EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

54th Annual ESPE Meeting 2015

 

1 - 3 October 2015 Barcelona, Spain
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N. Poster
Poster title
Applicant name
Status
  1-P1 Evaluation of Glucose Metabolism and Cardiovascular Risk Factors and Hyperandrogenemia in Prepubertal Girls with Premature Pubarche D&304;GDEM BEZEN Received Received
  2-P1 ONTOGENY OF THE SYNCHRONIZATION BETWEEN ADRENAL CLOCK GENES, ADRENAL STEROIDOGENESIS-RELATED GENES AND THE CIRCADIAN RHYTHM OF THE HPA AXIS IN RATS Ayrton Moreira Received Received
  3-P1 Are heterozygous carriers of CYP21A2 less vulnerable to psychological stress? Anna Nordenstrm Received Received
  4-P1 Effect of CYP17A1 inhibitors orteronel and galeterone on adrenal androgen biosynthesis. Sameer S. Udhane Received Received
  6-P1 Genetic diagnosis of congenital primary adrenal insufficiency by Massive Parallel Sequencing (MPS). Florence Roucher Boulez Received Received
  7-P1 Carriers of 21- Hydroxylase Deficiency Demonstrate Increased Psychological Vulnerability to Stress Eleni Magdalini Kyritsi Received Received
  8-P1 CORTISOL CORTISONE RATIO AND METALLOPROTEINASE-9 EMERGING AS RISK FACTORS ASSOCIATED WITH PEDIATRICS HIPERTENSION Constanza Pinochet Received Received
  9-P1 Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia (CLAH) due to StAR Mutations Abdulsalam Abu-Libdeh Received Received
  10-P1 Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Receptor in Neonates Steven Ghanny Received Received
  11-P1 Steroid 11-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases Mohammad Ahmad Awwad Alqahtani Received Received
  12-P1 GENETIC DIAGNOSIS USING WHOLE EXOME ANALYSIS IN TWO CASES WITH MALIGN INFANTILE OSTEOPETROSIS Korcan Demir Received Received
  13-P1 Osteogenesis imperfecta - a pilot trial on treatment with the RANKL-antibody Denosumab Heike Hoyer-Kuhn Received Received
  14-P1 No secular trend in vitamin D levels over the past 30 years in Swedish children Bjrn Andersson Received Received
  15-P1 Lithium chloride prevents glucocorticoid-induced growth failure in cultured fetal rat metatarsal bones Ondrej Soucek Received Received
  16-P1 Diverse presentations of hypophosphatasia in pediatric patients: a review of the case literature Kristina Kolygo Received Received
  17-P1 Humanin prevents undesired apoptosis of chondrocytes without interfering with the anti-inflammatory effect of dexamethasone in a model of arthritis Bettina Sederquist Received Received
  18-P1 RESPONSE TO VITAMIN D REPLACEMENT IS DETERMINED BY BODY SURFACE AREA IN CHILDREN WITH VITAMIN D DEFICIENCY In Hyuk Chung Received Received
  21-P1 Effects of inorganic phosphate and FGF23 on C2C12 myoblast cells Adalbert Raimann Received Received
  22-P1 EVALUATION OF BONE MINERAL DENSITY AND MICROARCHITECTURAL PARAMETERS BY DXA AND HR-pQCT IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS FROM A SINGLE-CENTER STUDY Guido de Paula Colares Neto Received Received
  23-P1 Safety and efficacy of treatment with long-acting lanreotide autogel in early infancy in patients with congenital hyperinsulinism Heike Corda Received Received
  24-P1 The influence of miR-125b in pancreatic -cell apoptosis Bei Han Received Received
  25-P1 Lower Bone Mineral Density in type 1 Diabetes Mellitus (T1DM) is probably associated with Wnt/-catenin pathway downregulation through increased Dickkopf-1 levels Kyriaki Karavanaki Received Received
  26-P1 Human Placenta-Derived Mesenchymal Stem Cells: a novel protocol for pancreatic differentiation. Viviana Dora Patianna Received Received
  27-P1 Activation of insulin signaling in gastrocnemius after central leptin infusion is associated with an increase in proliferation and muscle fiber size Vicente Barrios Received Received
  28-P1 Clinical characterisation of a novel RFX6 mutation- a rare cause of neonatal diabetes syndrome Moira Cheung Received Received
  29-P1 Is reduced heart rate variability associated with arterial stiffness in youth with childhood-onset type 1 diabetes mellitus? Hwa Young Kim Received Received
  30-P1 A NOVEL MUTATION IN THE ABCC8 GENE CAUSING A VARIABLE PHENOTYPE OF IMPAIRED GLUCOSE METABOLISM IN THE SAME FAMILY Maines Evelina Received Received
  31-P1 Type 1 Diabetes Onset: a story of innate and adaptive immune cells? Ana Laura Fitas Received Received
  32-P1 Etiological diagnosis of diabetes in Italian diabetic children and adolescents Delvecchio Maurizio Received Received
  33-P1 Improved genetic testing for monogenic diabetes in the Swiss population by targeted next generation sequencing Mirjam Dirlewanger Received Received
  34-P1 Low bone mineral density is associated to poor glycemic control and increased dickkopf-1 (DKK-1) serum levels in children and adolescents with type 1 diabetes Maria Felicia Faienza Received Received
  35-P1 Effect of 6 months therapy with Metreleptin in an African American boy with Congenital generalized lipodystrophy. Svetlana Ten Received Received
  36-P1 Somatic paternal UPD on chromosome 11p15 in focal form of congenital hyperinsulinism (CHI) causes monoallelic expression of mutant ABCC8 and KCNJ11 Ina Dallmann Received Received
  37-P1 Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria Axel Dost Received Received
  38-P1 METABOLIC SYNDROME FREQUENCY IN LONGITUDINALLY FOLLOWED CHILDREN WITH PREMATURE ADRENARCHE DURING PUBERTAL AGES Feyza Darendeliler Received Received
  39-P1 EVALUATION OF ABILITY OF URINARY PODOCALYXIN, NEPHRIN AND LIVER TYPE FATTY ACID BINDING PROTEIN FOR EARLY DIAGNOSIS IN RENAL INJURY IN ADOLESCENTS WITH TYPE 1 DIABETES Seniha Kiremitci Yilmaz Received Received
  40-P1 Efficacy and safety of a fixed combination of insulin degludec/ insulin aspart in children and adolescents with type 1 diabetes Jodi Cusack Received Received
  41-P1 Current care and outcomes for children and young people with diabetes in England and Wales: Results from the National Paediatric Diabetes Audit Naomi Holman Received Received
  42-P1 Dynamics perceptions of their own health in the process of learning self-control adolescents with type 1 diabetes mellitus Olena Budreiko Received Received
  43-P1 Evaluation of median nerve in children with type1 diabetes using ultrasonographic imaging andelectrophysiology Nancy Elbarbary Received Received
  44-P1 Is metabolic control affected by military service in young adults with type 1 diabetes? Avivit Brener Received Received
  45-P1 IMMUNE/INFLAMMATORY PROFILE IN CHILDREN WITH TYPE 1 DIABETES MELLITUS AND CELIAC DISEASE AND/OR AUTOIMMUNE THYROIDITIS Valentina Fattorusso Received Received
  46-P1 Trends in insulin therapy in 50,861 children and adolescents with type 1 diabetes from Austria and Germany between 2000 and 2014 Barbara Bohn Received Received
  47-P1 RELATIVE HYPOALDOSTERONISM IN A PATIENT WITH WOLCOTT-RALLISON SYNDROME Ahmet Ucar Received Received
  48-P1 Structured Education Programmes for Children with Type 1 Diabetes A Systematic Review Anbezhil Subbarayan Received Received
  49-P1 Can hypothalamic obesity be treated with stimulants? -Follow up Friederike Denzer Received Received
  50-P1 A feasibility study of intra-gastric balloons (supported by a lifestyle programme) for the treatment of severe adolescent obesity - the (BOB) Study. pooja sachdev Received Received
  51-P1 Distribution of obesity indices among European preschool children and associated risk factors: the ToyBox-study Sonya Galcheva Received Received
  52-P1 A Randomized Trial of the Effects of Perinatal Education of Overweight Pregnant Women to Prevent Childhood Overweight: the ETOIG study. Veronique NEGRE Received Received
  53-P1 Perypheral neuroblastic tumors and ROHHADNET syndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumor) FLAVIA NAPOLI Received Received
  54-P1 bestPWS EU: A Phase 3 study in adolescent and adult patients with PWS in Europe Nerissa Kreher Received Received
  55-P1 Intrauterine growth restriction is associated with greater severity in childhood obesity-associated metabolic impairment and poorer adult height prediction Martos-Moreno Gabriel Á. Received Received
  56-P1 Immunohistochemical detection of estrogen a and androgen receptors in genital tissues in girls with congenital adrenal hyperplasia Maria Kareva Received Received
  57-P1 Attitudes of parents of Klinefelter boys and Flemish pediatricians towards neonatal screening and fertility preservation techniques in Klinefelter syndrome. Inge Gies Received Received
  58-P1 Long-Term Endocrine Outcome In Men With Partial Androgen Insensitivity Syndrome Angela Lucas-Herald Received Received
  59-P1 Novel Genetic Associations In Children With Disorders Of Sex Development (DSD) And Neurodevelopment Disorders Insights From The Deciphering Developmental Disorders (DDD) Study Gabriella Gazdagh Received Received
  60-P1 Insight into the Human Ovarian Sex Development Networks Bouzzi Leila Received Received
  62-P1 Prediction of germ cell cancer occurrence in postpubertal individuals with androgen insensitivity based on pathological findings and cancer predisposition SNPs Martine Cools Received Received
  63-P1 Gender identity prediction in adulthood by HTP test (House-Tree-Family) in 46, XY DSD patients Rafael Loch Batista Received Received
  64-P1 MAMLD1 mutations seem not sufficient to explain a 46,XY DSD phenotype. What else? Camats Tarruella Núria Received Received
  65-P1 Subcutaneous continuous administration of recombinant human luteinizing and follicle-stimulating hormones is an effective treatment for micropenis during the mini-puberty Stoupa Athanasia Received Received
  66-P1 46,XX ovotesticular DSD in the absence of SRY gene associated to SOX3 duplication Romina P. Grinspon Received Received
  67-P1 miR-146a-mediated suppression of the inflammatory response in human adipocytes Julian Roos Received Received
  68-P1 Leptin resistance alteration after modulation of dopamine system funcional activity in rats diet-induced obesity Liudmila Viazava Received Received
  70-P1 Outcome of Adolescents Undergoing Sleeve Gastrectomy One Year Follow-up Michal Ben-Ami Received Received
  71-P1 Identifying critical periods for maintaining weight loss in obese children Amanda Peacock Received Received
  72-P1 Use of topiramate in severe hyperphagia associated to neuropsychiatric features in a boy with congenital proopiomelanocortin deficiency (POMC) Stefania Pedicelli Received Received
  73-P1 CIRCULATING miR146a AND 486-5p ARE ALTERED IN OBESE CHILDREN WITH AND WITHOUT NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) AND CORRELATE WITH ABDOMINAL FAT AND BMI. Maria Elisabeth Street Received Received
  75-P1 Ghrelin and brain-derived neurotrophic factor in children with Prader-Willi syndrome. Elena Bogova Received Received
  76-P1 Endothelial Progenitor Cells in Obese Non-Diabetic Children and Adolescents: Relations to Some Metabolic Parameters, Echocardiographic Parameters and Tissue Doppler Imaging Alaa Ahmed Received Received
  77-P1 Evaluation of adiponectin concentrations in obese children and its correlation with lipid and carbohydrate parameters Ruminska Malgorzata Received Received
  78-P1 Genetic Polymorphisms as Predictive Markers of Response to Growth Hormone Therapy in Paediatric Growth Hormone Deficiency Anna-Maria Jung Received Received
  79-P1 Decrease of jumping power in adolescents with severe GHD (sGHD) after stop of GH-therapy Roland Schweizer Received Received
  80-P1 GOOD CLINICAL RESPONSE TO GROWTH HORMONE THERAPY IN A BOY WITH A COMBINATION OF FAMILIAR SHORT STATURE CAUSED BY NOVEL p.Val478Serfs14 MUTATION IN ACAN GENE AND ISOLATED GROWTH HORMONE DEFICIENCY Stepanka Pruhova Received Received
  81-P1 The growth response to growth hormone treatment is greater in patients with SHOX enhancer deletions compared to SHOX defects. Stephany Donze Received Received
  82-P1 Assessment of Primary Cancers in Growth Hormone (GH)Treated Paediatric Patients Compared with General Population Registries: An Epidemiological Analysis of a Large, Multinational, Prospective Observational Study Christopher Child Received Received
  83-P1 Genetic markers contribute to the Prediction of response to GH in severe but not mild GH deficiency Adam Stevens Received Received
  84-P1 Disease and Treatment Burden In Children And Adolescents with Growth Hormone Deficiency (GHD) Michael Maddalena Received Received
  85-P1 EFFECTS OF GROWTH HORMONE TREATMENT ON IMMUNITY María Dolores Cañete Vázquez Received Received
  86-P1 The growth hormone treatment results in the increase of irisin concentration in plasma Beata Wikiera Received Received
  87-P1 A novel OTX2 gene mutation in a child with growth hormone deficiency Maurizio Delvecchio Received Received
  88-P1 The dose dependent effect of growth hormone therapy in patients with IGF-1 receptor haploinsufficiency due to heterozygous deletion Haruo Mizuno Received Received
  89-P1 Royal Jelly supplementation induces the growth plate development and increases plasma growth hormone and estradiol levels in prepubertal rats Ozgur Pirgon Received Received
  90-P1 Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C Shinichi Nakashima Received Received
  91-P1 Mutation in RTTN, a regulator of ciliary function, causes a complex syndrome characterized by severe congenital microcephaly, lissencephaly and profound growth failure in two siblings Anna Grandone Received Received
  93-P1 Severe IGF-I deficiency and multi-organ autoimmune disease associated with novel germline STAT3 mutations. Horacio Domene Received Received
  95-P1 Various imprinting disorders underlying Silver-Russell Syndrome-compatible phenotype Masayo Kagami Received Received
  96-P1 Ligase IV deficiency syndrome as a cause of microcephalic primordial dwarfism in dizygotic twins Celine Girardin Received Received
  97-P1 HIGH FREQUENCY OF HYPOMORPHIC ALLELIC HAPLOTYPES OF THE GH1 PROXIMAL PROMOTER IN PATIENTS WITH PROPORTIONAL UNDERGROWTH AND ISOLATED GH DEFICIENCY Angel Campos-Barros Received Received
  98-P1 Growth Hormone Excess in McCune-Albright Syndrome Daniele Tessaris Received Received
  99-P1 Growth hormone hypersecretion in children with NF1 and optic pathway gliomas Stefania Pedicelli Received Received
  100-P1 Atypical features in patients with Leprechaunism suggesting a wide clinical spectrum of disease Harshini Katugampola Received Received
  101-P1 Does Type 1 childhood diabetes start in utero? Zvi Laron Received Received
  102-P1 The role of HNF1B in human pancreas development and diabetes Ranna El Khairi Received Received
  103-P1 Molecular Characterization of a Novel Non-Stop KCNJ11 Mutation Associated with a Dual Focal and Diffuse Hyperinsulinaemic Hypoglycaemia Phenotype Ved Bhushan Arya Received Received
  104-P1 Diazoxide Responsive Congenital Hyperinsulinism in a Patient with Dual Genetic Aetiology (HNF4A and ABCC8 mutation) Dinesh Giri Received Received
  105-P1 Fluoxetine induced Hypoglycemia in a patient with Congenital Hyperinsulinism on Lanreotide Therapy Dinesh Giri Received Received
  106-P1 Influence of nocturnal glycemia on ventricular repolarization and heart rate variability in prepubertal children with type 1 diabetes. Marie-Béatrice SAADE Received Received
  107-P1 CHANGES IN SERUM PROTEIN EXPRESSION IN SMALL-FOR-GESTATIONAL-AGE NEWBORN INFANTS AT DIFFERENT GESTATIONAL AGES Ramón Cañete Estrada Received Received
  108-P1 Liver ER stress and Intrauterine growth retardation in rats Annalisa Deodati Received Received
  109-P1 Continuous subcutaneous infusion of recombinant LH and FSH during early infancy promotes testicular descent in congenital hypogonadotropic hypogonadism. Anne Sophie LAMBERT Received Received
  110-P1 Neonatal screening program for Central Congenital Hypothyroidism Debora Braslavsky Received Received
  111-P1 Serum Neurokinin B level can be used to differentiate central precocious puberty from premature thelarche. Mesut Parlak Received Received
  112-P1 Etiological spectrum and clinical characteristics of 129 children with gonadotropin independent precocious puberty: A nationwide cohort study Zeynep Atay Received Received
  113-P1 Relevance of astrocytic signals for GnRH-neuronal function Sabine Heger Received Received
  114-P1 Screening of mutations in idiopathic hypogonadotropic hypogonadism using a targeted next-generation sequencing approach Maria Naumova Received Received
  116-P1 FSHB/FSHR genetic variants alter serum FSH levels and prepubertal ovarian follicular growth in healthy girls Alexander Busch Received Received
  117-P1 The Puberty Nomogram and Transient Breast Budding in Healthy Girls Marie Lindhardt Johansen Received Received
  118-P1 Specific hypothalamic activation pattern by mGlu5 receptor blockade in vivo during pubertal development in female mice Ioana Inta Received Received
  119-P1 Lipid profiles in gender dysphoric adolescents treated with GnRH agonists alone and in combination with cross-sex hormones Sebastian Schagen Received Received
  120-P1 A novel LHX4 mutation is associated with hypogonadotropic hypogonadism, not combined pituitary hormone deficiency Masaki Takagi Received Received
  121-P1 A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty Johanna Knskoski Received Received
  122-P1 Congenital hypothyroidism in twin couples and triplets Antonella Olivieri Received Received
  123-P1 Th17 cells in children with Graves disease during methimazole treatment Klatka Maria Received Received
  124-P1 Thyrocytes are particularly well protected against oxidative stress induced by H2O2 ghaddhab chiraz Received Received
  126-P1 Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born after In Vitro Fertilisation (IVF) Vassiliki Giogli Received Received
  127-P1 Transient vs. Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-term Data Can Help Formulate a Practical Prognostic Algorithm Vassiliki Giogli Received Received
  128-P1 Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor Alpha Mutations Korcan Demir Received Received
  129-P1 Intelligence and behaviour in children and adolescents with Hashimotos thyroiditis Claudia Boettcher Received Received
  130-P1 Brain-lung-thyroid syndrome - clinical update on a heterogeneous disorder Nina Lenherr Received Received
  131-P1 Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis Malgorzata Kumorowicz-Czoch Received Received
  132-P1 A severe hyperthyroidism in an infant revealed a familial nonautoimmune hyperthyroidism with novel heterozygous thyrotropin receptor gene mutation. isabelle oliver petit Received Received
  134-P1 Coexistence of FOXE1 and BMP15 gene variants in young females withpremature ovarian insufficiency: Evidence of digenic inheritance NIKOLAOS SETTAS Received Received
  135-P1 Sex hormones and gonadal size in pubertal girls born small or appropriate for gestational age Indre Petraitiene Received Received
  136-P1 The methylation level of the Eap1 promoter is different during pubertal development in normal weight and obese female rats Sabine Heger Received Received
  138-P1 Weight gain in Turner Syndrome: Association to puberty induction? Christina Toschke Received Received
  139-P1 A study of arterial stiffness in Turner syndrome patients using cardio-ankle vascular index Hae Woon Jung Received Received
  140-P1 Impaired motor function in Turner syndrome: what is the relationship to performal intelligence scores? Betl Taskin Received Received
  141-P1 Adult height after growth hormone treatment and its association with X chromosome dosage in Turner Syndrome: a cross-sectional database analysis of the French national rare disease network. Elodie Fiot Received Received
  142-P1 Fracture incidence is not associated with the 6-year development of trabecular BMD in paediatric Turner syndrome patients Ondrej Soucek Received Received
  144-P1 Primary Adrenal Insufficiency in childrenwithout congenital adrenal hyperplasia:Molecular and clinical characterization of a nationwide cohort Tulay Guran Received Received
  145-P1 Clinical follow-up of the first SF-1 deficient female patient Karine Gerster Received Received
  146-P1 Salt sensitivity of blood pressure at age 7-8 years in preterm born children. Charlotte Ruys Received Received
  147-P1 A new LC-MS/MS assay for the analysis of sulfated steroids in human serum: quantification of cholesterol sulfate, pregnenolone sulfate, 17-hydroxypregnenolone sulfate and androgen sulfates Alberto Sánchez-Guijo Received Received
  148-P1 The analysis of occurrence the zinc transporter antibodies ZnT8 in children with Graves disease and Hashimotos thyroiditis. Artur Bossowski Received Received
  149-P1 Recombinant Parathyroid Hormone (1-34) replacement treatment of Hypoparathyroidism in the alfacalcidol-resistant patient with severe Autoimmune Polyendocrinopathy Syndrome type 1 Leila Sozaeva Received Received
  151-P1 A case of autoimmune polyglandular syndrome type I presenting as progressive generalized lipodystrophy in a 15-month-old child. Ekaterina Sorkina Received Received
  152-P1 Noonan syndrome-causing SHP2 mutant inhibits murine growth plate chondrogenesis and bone development: role of Ras/MAPK hyperactivation Thomas Edouard Received Received
  153-P1 Relationship between Vitamin D and Brainstem Auditory Evoked Potentials (BAEPs) Murat Do&287;an Received Received
  154-P1 Novel Compound Heterozygous BMP1 variants associated with Osteogenesis Imperfecta Rimm Huh Received Received
  155-P1 Prospective Cognitive Assessment in Children with Craniopharyngiomaat Diagnosis, after Conservative Surgery and Before and after Adjuvant Radiation. Penelope Rodriguez-Cabrera Received Received
  156-P1 CUSHING SYNDROME DUE TO ADRENOCORTICAL CARCINOMA IN A 3 MONTH OLD INFANT WITH A LARGE INTERSTITIAL DELETION OF CHROMOSOME 5Q INCLUDING THE APC GENE Halit Ilker Akkurt Received Received
  157-P1 How do Adolescent Minors Banking Sperm Before Cancer Therapy Subsequently Use the Fertility Service? A Post Banking Re-evaluation. Maria Michaelidou Received Received
  158-P1 The Expression of Related Neuroendocrine Factors with Puberty Onset in Rat at Different Developmental Stages Mo Kyung Jung Received Received
  159-P1 FOXL2 gene and combined pituitary hormone deficiency: a possible link Saarh Castets Received Received
  160-P1 Septo-optic dysplasia (SOD) associated with Koolen-de Vries syndrome (KDVS): a case report Ani Aroyo Received Received
  161-P1 Screening of IGSF1 in patients with Central Hypothyroidism and GH deficiency, participating in the Dutch HYPOPIT study Laura de Graaff Received Received
  162-P1 Congenital Hypothyroidism: Reduction in the Female to Male Ratio Following the Decrease of the TSH Cut-off Point Used for Neonatal Screening Antonis Voutetakis Received Received
  163-P1 Pediatric Thyroid Nodule Score (PTNS): Derivation and Validation of a Predictive Score for Thyroid Nodule Assessment in Children Danielle van der Kaay Received Received
  164-P1 Practical application of elastography in the diagnosis of thyroid nodules in children. Hanna Borysewicz Received Received
  165-P1 Higher urinary iodine levels correlates with lower systolic blood pressure in Chilean schoolchildren Francisca Grob Received Received
  166-P2 Late diagnosis of adrenal insufficiency caused by novel compound heterozygous mutations in POMC. Elena Frolova Received Received
  167-P2 Hyponatraemia secondary to exudative eczema Irene Pilar Fernandez Viseras Received Received
  168-P2 The Natural Mutant Receptor hGRaT556I Causes Primary Generalized Glucocorticoid Resistance Through Decreased Affinity for the Ligand and Impaired Interaction with the GRIP1 Coactivator NICOLAS NICOLAIDES Received Received
  169-P2 References values under Synacthen test for 6 steroids in serum by LC-MS/MS ingrid Plotton Received Received
  170-P2 Usefulness of salivary cortisol levels in secondary adrenal insufficiency in pediatric population Raquel Corripio Received Received
  171-P2 Acute adrenal failure in a term newborn with congenital cytomegalovirus infection: case description and review of the literature Malgorzata Wasniewska Received Received
  172-P2 Resveratrol disrupts steroidogenesis in human fetal adrenals Iuliia Savchuk Received Received
  174-P2 CLINICAL, BIOCHEMICAL AND MOLECULAR CHARACTERISTICS OF THE PATIENTS WITH NONCLASSICAL CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY IN CROATIA Nevena Krnic Received Received
  176-P2 Triple A syndrome - the second most common cause of chronic adrenal insufficiency in North Africa? asmahane ladjouze Received Received
  177-P2 Analysis the relationship between clinical characteristics and genotype of six cases of Bartter syndrome and Gitelman syndrome in children jun zhang Received Received
  178-P2 Genotypic heterogeneity and clinical phenotype in two patients with triple A syndrome (AAAS). Antonella Meloni Received Received
  179-P2 Primary adrenal insufficiency: About a pediatric series Imen Nardine Received Received
  180-P2 High-dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-hydroxylase deficiency Mesut Parlak Received Received
  181-P2 Baseline cortisol concentrations predict positively and negatively anti- and pro- oxidation, respectively that are measured following an acute aerobic exercise bout in pre- and early pubertal normal-weight and obese boys. George Paltoglou Received Received
  182-P2 Insulin sensitivity and adipocytokynes in children with Classical Congenital Adrenal Hyperplasia Nicola Improda Received Received
  183-P2 24-hour urinary free cortisol as a screening test for Cushings syndrome in children. Lucy Shapiro Received Received
  184-P2 Familial Hyporeninemic Hyperkalemia and Hypertension (Pseudohypoaldosteronism Type II) in Infancy and Childhood. Aaron Hanukoglu Received Received
  185-P2 Severe craniosynostosis syndrome associated to salt wasting congenital adrenal hyperplasia Cristiane Kopacek Received Received
  186-P2 TESTICULAR ADRENAL CELL REST TUMORS ARE NOT ASSOCIATED WITH 21 HYDROXYLASE MUTATIONS OR THERAPY COMPLIANCE IN BOYS WITH CLASSIC FORM OF CAH Mirjana Kocova Received Received
  187-P2 A large family with a novel mutation in the SCNN1A gene causing a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) Alexandra Efthymiadou Received Received
  188-P2 Phosphoglucomutase -1 deficiency presented as adrenal insufficiency Neta Loewenthal Received Received
  189-P2 The etiological spectrum of congenital adrenal hyperplasia based on molecular genetic analyses Jin-Ho Choi Received Received
  190-P2 Higher serum DHEAS concentration is associated with lower plasma LDL cholesterol concentration in children Aino Mntyselk Received Received
  191-P2 Central adrenal insufficiency is not a common feature in CHARGE syndrome Gianni Bocca Received Received
  193-P2 Adrenal function in children born small for gestational age Indre Petraitiene Received Received
  194-P2 Cushings syndrome in children and adolescents : About a pediatric serie Aicha houatia Received Received
  195-P2 Serum cortisol and cortisone ratio as sensitive tool to identify subjects with severe or partial 11-hydroxysteroid dehydrogenase type 2 deficiency Cristian Carvajal Received Received
  196-P2 The role of de Nurse practitioner in optimizing care for Children with Congenital Adrenal Hyperplasia Viviane van de Crommert Received Received
  197-P2 Evaluation of medical treatment in the first 2 years of life with a new Dutch national longitudinal registry for children with congenital adrenal hyperplasia (CAH) Annelieke van der Linde Received Received
  199-P2 CARDIO-METABOLIC RISK FACTORS IN CHILDREN AND ADOLESCENTS WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY Taninee Sahakitrungruang Received Received
  200-P2 A novel mutation (c.delG209) in the proopiomelanocortin (POMC) gene in a child with early-onset obesity Semra etinkaya Received Received
  201-P2 IMPROVED LINEAR GROWTH IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA. Carla Bizzarri Received Received
  202-P2 Autoimmune polyglandular syndrome type 1 in Russia: clinical experience in 112 patients. Elizaveta Orlova Received Received
  203-P2 Autoimmune encephalitis - a newly recognised clinical manifestation of autoimmune polyendocrine syndrome type 1? Juliana Ferenczova Received Received
  205-P2 Mechanism of bone disease in Prader-Willi syndrome Maria Felicia Faienza Received Received
  206-P2 Hereditary vitamin D-resistant rickets (HVDRR): Report of four cases with successful use of intermittent intravenous calcium via peripheral route SAYGIN ABALI Received Received
  207-P2 A novel PRKAR1A gene mutation with mild brachydactyly Yagi Hiroko Received Received
  208-P2 Bone mineral density in children and adolescents with vertical HIV infection. Deisi Maria Vargas Received Received
  209-P2 Sclerostin and its associations with energy metabolism in children and adolescents Anna W&281;drychowicz Received Received
  210-P2 Genetic and epigenetic alterations at the GNAS locus and clinical consequences in Pseudohypoparathyroidism: a new healthcare pathway federica giachero Received Received
  211-P2 Fibrous cortical defects and non-ossifying fibromas in patients with precocious puberty Kyung-Sue Shin Received Received
  212-P2 The effect of high dose oral 17 estradiol on bone mineralization and body composition in young women with Turner syndrome - a 5 year randomized controlled clinical trial Line Cleemann Received Received
  213-P2 Comparison of cost benefits and efficacy of Zoledronic acid and Pamidronate in the treatment of Osteogenesis Imperfecta in children. Vrinda Saraff Received Received
  214-P2 TmP/GFR is a useful marker in making a clinical diagnosis of X-linked hypophosphatemic rickets caused by the PHEX gene mutation Ryojun Takeda Received Received
  215-P2 Whole body vibration training improves physical function and increases bone and muscle mass in youngsters with mild cerebral palsy Silmara Gusso Received Received
  216-P2 A CASE WITH ACRODYSOSTOSIS AND HORMONE RESISTANCE Selma Tun Received Received
  217-P2 The spectrum of molecular defects in 64 patients with hypophosphatemic rickets identified by targeted next-generation sequencing. Kristina Kulikova Received Received
  218-P2 NEPHROCALCINOSIS AND NEPHROLITHIASIS IN 36 X-LINKED HYPOPHOSPHATEMIC RICKETS PATIENTS: DIAGNOSTIC IMAGING AND EVALUATION OF RISK FACTORS IN A SINGLE-CENTER STUDY Guido de Paula Colares Neto Received Received
  220-P2 Genotype and phenotype characteristics in 22 patients with Vitamin D Dependent RicketsType I (VDDR1) Huseyin Demirbilek Received Received
  221-P2 Evidence of a link between resting energy expenditure and bone remodelling, glucose homeostasis and adipokine variations in adolescent girls with anorexia nervosa Mamoun laurent Received Received
  223-P2 Refractory Hypercalcaemia of Malignancy: Responsiveness to Denosumab and Zoledronate Dinesh Giri Received Received
  224-P2 Fractures In Boys With Duchenne Muscular Dystrophy And Their Relationship To Age Shuko Joseph Received Received
  225-P2 Early Detection of Increased Bone Turnover among Children and Adolescents with Type 1 Diabetes Mellitus Amina Abdelwahab Received Received
  226-P2 Association between oxidative stress and bone turnover markers in the obese children Pawel Matusik Received Received
  227-P2 Longitudinal bone development in patients with classical congenital adrenal hyperplasia: data using peripheral quantitative computed tomography Susanne Bechtold Received Received
  228-P2 Online Survey to Characterize the Burden of Illness in Children with X-linked Hypophosphatemia (XLH) Alison Skrinar Received Received
  229-P2 Comparison of the response to bisphosphonate treatment between acute lymphoblastic leukaemia and osteogenesis imperfecta type I Suma Uday Received Received
  231-P2 Cinacalcet treatment in girls with hereditary vitamin D resistant rickets Erkan Sari Received Received
  232-P2 Regulation of bone growth via ligand-specific activation of estrogen receptor alpha Maryam Iravani Received Received
  233-P2 Teriparatide (rhPTH) therapy in a boy with Hypoparathyroidism-Deafness-Renal dysplasia (HDR) syndrome due to GATA3 mutation Dinesh Giri Received Received
  234-P2 Variable degree of hormonal resistance in patients with Progressive Osseous Heteroplasia Kentaro Miyai Received Received
  235-P2 Assessment of foramen magnum in early infancy is efficient for patients with achondroplasia Chisumi Sogi Received Received
  236-P2 Body composition measures on different DEXA scanners are not the same Christiane Fritz Received Received
  237-P2 Intrauterine growth restriction, gestational age, steroidal prophylaxis and breastfeeding influence bone mass in prepubertal children ANNALISA CALCAGNO Received Received
  238-P2 Can vitamin D deficiency cause prolongation in visual evoked potentials? Murat Dogan Received Received
  239-P2 Novel CYP27B1 Gene Mutations in Children with Vitamin D-Dependent Rickets Type 1A Erdem Durmaz Received Received
  240-P2 Size-corrected bone mineral density is not affected by haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) in leukaemia survivors Christina Wei Received Received
  241-P2 Quantitative Sonometeric Bone Age (SBA) as a Function of Height and BMI Alina German Received Received
  242-P2 THE ASSOCIATION OF ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD) WITH THE MEAN PLATELET VOLUME (MPV) AND VITAMIN D Murat Dogan Received Received
  243-P2 Dyslipidemia in Children with Diabetes Pei Kwee Lim Received Received
  244-P2 Diabetes mellitus and hypoparathyroidism in a girl with mitochondrial disease Nurgun Kandemir Received Received
  245-P2 Association of ghrelin levels and insulin resistance in small for gestational age rats Wangkai Liu Received Received
  247-P2 A case of Donohue Syndrome : New Genetic Mutation and added phenotypic characteristics Fawziya Alyafei Received Received
  248-P2 Genetic analysis and follow-up of 25 neonatal diabetes mellitus patients in China Bingyan Cao Received Received
  250-P2 Recombinant human insulin-like growth factor-1 treatment in patients with insulin receptor mutations resulting in Donohue syndrome: a 10-year experience in a tertiary centre. Nicola Improda Received Received
  251-P2 Sick day rule: Survey of parents of children with Type 1 diabetes (experience and Knowledge) Chizo AGWU Received Received
  252-P2 Brachial Flow Mediated Dilation and its Relation to Osteoprotegerin in Type 1 Diabetes Mellitus Nermine Amr Received Received
  255-P2 Significant impact of nocturnal melatonin secretion on obesity-related metabolic disorders in children and adolescents Johanna Overberg Received Received
  256-P2 Exposure to phthalates and phenols in relation to gestational blood glucose homeostasis Benjamin Fisher Received Received
  257-P2 Developing a targeted, mobile-health technology (e-book) to promote self-care during diabetes transition Andrew DWYER Received Received
  258-P2 CARDIAC AUTONOMIC NEUROPATHY IS HIGHLY PREDICTIVE FOR SURVIVAL IN CHILDREN WITH MAURIAC SYNDROME Radka Savova Received Received
  259-P2 Predictors of Cystic Fibrosis-Related Diabetes (CFRD) in Patients with CF and Pancreatic Insufficiency Joseph Meyerovich Received Received
  260-P2 Adherence to diabetes care in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study. Renata Villoro Received Received
  261-P2 Gaining from patient experience on a local level: The introduction of annual questionnaires for children and teenagers with diabetes Emily Cottrell Received Received
  262-P2 Factitious administration of analogue insulin to a 2 year old child NEHAL THANAWALA Received Received
  263-P2 Insulin Sensitivity in Adolescents with Gender Dysphoria during Puberty Suppressing Therapy with GnRH Agonists Sebastian Schagen Received Received
  264-P2 Ethnic variation in the correlation of waist circumference to daily insulin requirement in children with type 1 diabetes Suma Uday Received Received
  265-P2 IMPORTANCE OF THROMBOCYTE VOLUME PARAMETERS IN TYPE I DIABETES MELLITUS PATIENTS WITH AND WITHOUT CLINICAL FINDINGS OF DIABETIC KETOACIDOSIS Dogus Vuralli Received Received
  266-P2 Increased Arterial Wall Stiffness in Children with Type 1 Diabetes and Poor Metabolic Control: An Early Marker of Vascular Complications? Barbora Obermannova Received Received
  267-P2 Glycaemic dysregulation in transfusion dependent thalassaemia patient in a childrens hospital SONG HAI LIM Received Received
  268-P2 MODY-GCK and MODY-HNF1A in children and adolescents in Russian population Elena Sechko Received Received
  269-P2 Clinical and hormonal profile in Mini-puberty of daughters born after pregnancies with diabetes: preliminary report JOEL RIQUELME Received Received
  270-P2 Growth and Endocrinopathy in Wolfram Syndrome: the experience of a nationally commissioned specialist clinic. Melanie Kershaw Received Received
  271-P2 Evaluation of a Novel Tool to Adjust Insulin Boluses based on Continuous Glucose Monitoring Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool) in Children and Youth with Type 1 Diabetes using Insulin Pump Therapy Emmeline Heffernan Received Received
  273-P2 Utility of estimated glucose disposal rate and fat mass percentage for predicting metabolic syndrome in children and adolescents with type 1 diabetes Cengiz Kara Received Received
  274-P2 Friedreichs Ataxia presenting with Diabetes Mellitus in an adolescent Serpil Bas Received Received
  275-P2 DO PANCREATIC FUNCTIONS PREDICT CARDIAC AND LIVER IRON LOADING IN TRANSFUSION-DEPENDENT BETA THALASSEMIA MAJOR PATIENTS USING CARDIOVASCULAR AND LIVER T2-STAR (T2)MAGNETIC RESONANCE ? Nancy Elbarbary Received Received
  276-P2 Determinants of outcome of children with type 1 diabetes in Cameroon. Loveline Lum Niba Received Received
  277-P2 Psychosocial Screening in children with Type 1 Diabetes in Ireland Elena Hennessy Received Received
  278-P2 Neonatal Diabetes Experience from a single center in Sri Lanka Navoda Atapattu Received Received
  279-P2 Dive: a serious game for diabetes therapeutic education in children Cecile Godot Received Received
  280-P2 GLUCOSE AND INSULIN RESPONSE AT STANDARD ORAL GLUCOSE LOAD AND FOLLOWED SUBMAXIMAL TREADMILL TEST IN OBESE ADOLESCENTS Tetyana Chaychenko Received Received
  281-P2 Insulin Dynamics and Biochemical Markers for Predicting Impaired Glucose Tolerance in Thai Obese Youth Taninee Sahakitrungruang Received Received
  282-P2 Total-Body Irradiation is a major risk factor for young adult onset diabetes mellitus and hyperlipidemia in childhood cancer survivors after hematopoietic stem cell transplantation. Ryuichi Nakagawa Received Received
  283-P2 Variables in Diabetic Children and Adolescents associated with High, Acceptable and Low range of Glycosylated Haemoglobin (HbA1c) in a DGH setting An Analysis Karthi Manoharan Received Received
  284-P2 In-patient care for children with type 1 diabetes- a regional audit in the Yorkshire and Humber region in the north of England. Suma Uday Received Received
  285-P2 Implementation of Effective Transition from Paediatric to Adult Diabetes Care: Epidemiological and clinical characteristics. A pioneering experience in North Africa. ESSADDAM Leila Received Received
  287-P2 Incidence of Type 1 Diabetes among Korean Children and Adolescents in 2012-2013: Analysis of Data from the Nationwide Registry of Korea Jae Hyun Kim Received Received
  289-P2 LONGITUDINAL STUDY OF IRISH CHILDREN AND ADOLESCENTS ON CONTINUOUS SUBCUTANEOUS INSULIN INFUSION (CSII) Mary-Ellen Bohane Received Received
  290-P2 C peptide variation after the diagnosis of type 1 diabetes in pediatric age Joana Correia Received Received
  292-P2 Incidence of Type 1 Diabetes in Children Under 15 years old in Navarre (Spain) Between 1980 and 2014 María Chueca Received Received
  293-P2 QUALITY OF LIFE IN ADOLESCENT WITH TYPE 1 DIABETES (T1D) AND ITS RELATIONSHIP WITH METABOLIC CONTROL GRACIA M. LOU-FRANCÉS Received Received
  294-P2 The prevalence of different subtypes of maturity-onset diabetes of the young in Russian Federation as defined by targeted next-generation sequencing Olesya Gioeva Received Received
  295-P2 Sirolimus therapy in infants with congenital hyperinsulinism after near total pancreatectomy Keun Hee Choi Received Received
  296-P2 Children born from mothers with gestational diabetes mellitus are at higher risk of metabolic derangement Reiko Horikawa Received Received
  297-P2 GH promotes mRNA expression and secretion of progranulin in 3T3-L1 cells. Song Guo Received Received
  298-P2 Early Diagnostics of Wolfram Syndrome Abdushelishvili Nino Received Received
  299-P2 Improving glycaemic control at diagnosis of type 1 diabetes: insulin dosing depending on degree of ketonaemia at presentation Sarah Kiff Received Received
  300-P2 Non-immune diabetes mellitus and neurodegeneration: two distinct cases of Wolfram syndrome. Annelies Lemay Received Received
  301-P2 EVALUATION OF CONTINUOUS GLUCOSE MONITORING IN CYSTIC FIBROSIS PATIENTS Laura Bilbao Received Received
  302-P2 The Impact of Diurnal Glycemic Variability on the Cardiovascular Systemin Children with Type 1 Diabetes Mellitus Oleg Dianov Received Received
  303-P2 Multiple malformations extending the phenotypic spectrum of Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency due to two novel mutations of the POR gene Aleksandra Janchevska Received Received
  305-P2 www.steroidogenicfactor-1.info: An online database of variants in steroidogenic factor-1 (SF-1, NR5A1) and resource for families and professional healthcare providers John Achermann Received Received
  306-P2 Two testes and 2 X chromosomes Why?AL JASER, FAHED, WHERRETT, DIANE. Division of Endocrinology, Department of Pediatrics,Hospital for Sick Children, University of Toronto, ON. fahed Aljaser Received Received
  308-P2 MAP3K1 mutation in a patient with complete XY gonadal dysgenesis Birgit Khler Received Received
  309-P2 Alterations in Germ Cell Memory and Mini-Puberty Induce Infertility in Cryptorchidism Faruk Hadziselimovic Received Received
  310-P2 Management of gonads in adults with androgen insensitivity: an international survey Ellen Maris Received Received
  311-P2 The localization of cells with XX and XY in gonadal tissues associated with ovotesticular disorder of sexual development with a 46,XX/46,XY karyotype Noriko Nishina Received Received
  312-P2 Birth Weight in Different Aetiologies of Disorder of Sex Development SUKRAN POYRAZOGLU Received Received
  313-P2 A novel human CYP19A1 deletion-insertion mutation reveals that the C-terminus of the aromatase protein is crucial for its activity asmahane ladjouze Received Received
  314-P2 Pubertal virilization in two unrelated XY teenagers with female phenotype due to NR5A1/SF-1 gene mutation Pascal PHILIBERT Received Received
  315-P2 Chimerism in a teenager with ovotesticular disorder of sexual development (DSD) Mihaela Buzduga Received Received
  317-P2 Next-generation Sequencing as a Rapid Molecular Diagnosis in Patients with 46,XY Disorder of Sex Development (DSD) Samim Ozen Received Received
  319-P2 Gonadotropin surge during the early postnatal activation period in 46,XX testicular/ovotesticular disorder of sex development (DSD) patients Mariana Costanzo Received Received
  320-P2 The Evaluation of AR and SRD5A2 Gene Mutations in 87 Patients with 46, XY DSD Children in Turkey Nese Akcan Received Received
  321-P2 Familial mutation of NR5A1/SF-1 gene associated with 46,XY DSD and spleen agenesis: a new syndrome? Pascal Philibert Received Received
  322-P2 Clinical spectrum of 45,X/46,XY mosaicism and variants in children. Hae Woon Jung Received Received
  323-P2 Chromosomal variations in children and adolescents with gender dysphoria: is routine karyotyping indicated? Gary Butler Received Received
  324-P2 DSD 46,XY and serum steroid profile ambiguity due to combined 17-beta hydroxysteroid dehydrogenase/21-hydroxylase deficiencies Elena Kuznetsova Received Received
  325-P2 FREQUENCY OF CRYPTORCHIDISM AND AGE AT OPERATION IN HELSINKI AREA BETWEEN 2004 AND 2014 Ella Kohva Received Received
  327-P2 A novel mutation of anti-Mullerian hormone receptor gene in a male with Persistent Mullerian Duct Syndrome ghadir elias-assad Received Received
  328-P2 miR-122 and non-alcoholic fatty liver disease in prepubertal obese children elena inzaghi Received Received
  329-P2 Meteorin-like (METRNL) expression in human adipose tissue is associated with adipocyte hypertrophy and inflammation and is down-regulated during human adipogenesis Antje Körner Received Received
  330-P2 Abdominal fat distribution measured by Magnetic Resonance Imaging in 197 children aged 10 to 15 years correlation to anthropometry and Dual X-ray Absorptiometry Jeanette Tinggaard Received Received
  331-P2 Autonomic nervous system function assessed by heart rate variability in children and adolescents with long term follow up of craniopharyngioma Hae Woon Jung Received Received
  332-P2 SIRT1 and SIRT2 gene expression in peripheral blood mononuclear cells of obese children and adolescents and their relationship with metabolic parameters and insulin resistance Mitra Nourbakhsh Received Received
  334-P2 Childhood obesity negatively influences adult Leydig cell function Isabel Wagner Received Received
  335-P2 Network Coordinated Primary Care Intervention in obese children and adolescents: almost a decade of experience. Sophie Guilmin-Crépon Received Received
  336-P2 Diagnosing the metabolic syndrome in survivors of childhood haematopoietic stem cell transplantation and total body irradiation (HSCT/TBI) Christina Wei Received Received
  337-P2 Laparoscopic sleeve gastrectomy in adolescents: metabolic consequences. Marina Ybarra Received Received
  338-P2 A novel melanocortin 4 receptor (MC4R) gene mutation associated with early onset severe obesity. Meropi Toumba Received Received
  339-P2 Hypothalamic obesity, Hyperphagia and Hyperinsulinaemia: time for a paradigm shift in assumptions? Hoong-Wei Gan Received Received
  340-P2 Prevalence of scoliosis in a large cohort of pediatric and adolescent Prader-Willi Syndrome: a Scottish-Italian study Sara Ciccone Received Received
  341-P2 Palmitic acid could modify cognitive and behavioral functions through sex specific activation of hippocampal astrocytes Laura María Frago Received Received
  342-P2 Changes in insulin sensitivity in adolescents who underwent bariatric surgery: effects of laparoscopic sleeve gastrectomy and laparoscopic gastric banding. Gianpaolo De Filippo Received Received
  343-P2 Chronodisruption in Obese Children Saner Christoph Received Received
  344-P2 Configuring a Better Estimation of Obese Childrens Kidney Size Fahimeh Soheilipour Received Received
  345-P2 Early onset of adiposity rebound is associated with higher leptin concentrations in 12-year old children Satomi Koyama Received Received
  346-P2 Metformin treatment for obese children and adolescents with insulin resistance Zdravka Todorova Received Received
  347-P2 A double-blind, placebo-controlled comparison of cinnamon extract to metformin effects upon insulin resistance, apolipoprotein B/ apolipoprotein A1 ratio, and body mass index of obese adolescent girls with polycystic ovarian syndrome Shadab Salehpour Received Received
  348-P2 Pantoprazole treatment of Exogenous Obesity and Hyperinsulinism in Childhood Murat Dogan Received Received
  350-P2 The switch in eating behavior in infants with Prader-Willi syndrome is associated with an increase in the acylated to unacylated ghrelin ratio: Results of a longitudinal study Renske Kuppens Received Received
  351-P2 Domino liver transplantation for the pre-emptive therapy of compound heterozygous familial hypercholesterolemia : A case of 3-year-old girl Hioyuki Tanaka Received Received
  353-P2 A new mutation of PCSK1 revealed by neonatal malabsorptive diarrhea, panhypopituitarism and major obesity. Natacha BOUHOURS-NOUET Received Received
  355-P2 BERARDINELLI SEIP CONGENITAL LIPODYSTROPHY. A LIGTH OF HOPE. Maria Ruiz del Campo Received Received
  356-P2 Physical and metabolic evolution of obese children and adolescents after the attainment of intense weight reduction Gabriel Á. Martos-Moreno Received Received
  358-P2 Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children Ayhan Abaci Received Received
  359-P2 FTO rs9939609 polymorphism is associated with the presence of obstructive sleep apnoea in obese youth. Kung-Ting Kao Received Received
  360-P2 Increasing waist/height ratio and BMI Z-score are associated with increased comorbidities in obese youth, although neither accurately identifies those with abnormal glucose metabolism. Kung-Ting Kao Received Received
  362-P2 Nonalcoholic fatty liver disease and intestinal inflammation in obese children ZEHRA YAVAS ABALI Received Received
  363-P2 Sleep and weight status at 4 years in the Inma Asturias cohort ISOLINA RIAÑO-GALAN Received Received
  364-P2 Evaluation of acylated ghrelin and obestatin levels and ghrelin/obestatin ratio in obesity Maryam Razzaghy Azar Received Received
  365-P2 A novel MC4R mutation associated with infancy-onset obesity Damla Goksen Received Received
  367-P2 Residual excess weight difference between BMI 35-40 and BMI over 40 after laparoscopic sleeve gastrectomy in severely obese adolescents. Midterm outcomes. Jeannette Linares Received Received
  368-P2 Effect of visfatin on gene expression of insulin signaling molecules in SW872 Adipocytes Ruizhen Li Received Received
  369-P2 Childhood obesity and normocalcamia with a GNAS mutation also present in mother. Sharon Lim Received Received
  370-P2 Information technology (IT) supported treatment of obese children and their families: A pilot study lAllemand Dagmar Received Received
  371-P2 Prevalence and phenotype characterization of MC4R mutations in a large paediatric cohort Heike Vollbach Received Received
  372-P2 The effect of ABCA1 gene C69T single nucleotide polymorphism on dyslipidemia and insulin resistance in obese children &304;lker Tolga zgen Received Received
  373-P2 Obese 5-years olds remain obese at age 12. Satomi Koyama Received Received
  374-P2 Lifestyle habits and arterial hypertension in children and adolescents Andrea Paola Rojas Gil Received Received
  376-P2 Metabolic syndrome components of normal weight central obese adolescents in Korea stratified by waist to height ratio: Results from K-NHANES 2008-2010 WONKYOUNG CHO Received Received
  377-P2 The Effect of Exenatide on Weight and Appetite in Overweight Adolescents and Young Adults with Prader-Willi Syndrome Parisa Salehi Received Received
  378-P2 Early-onset obesity and adrenal insufficiency associated with a homozygous POMC mutation. Antonella Meloni Received Received
  379-P2 Clinical and Laboratory Differences between Metabolically Healthy and Unhealthy Obese Children Selin Elmaogullari Received Received
  380-P2 Insulin-resistance and abnormal glucose tolerance after paediatric hematopoietic stem cell transplantation in blood-cancer survivors. Sara Ciccone Received Received
  381-P2 Metformin in combination with lifestyle changes effectively reduces body mass index and waist circumference in overweight/obese children and adolescents Natalija Smetanina Received Received
  382-P2 Insulin-like factor 5 a novel orexigenic hormone in humans is dysregulated in obesity Isabel Wagner Received Received
  383-P2 TRYPTOPHAN SUPPLEMENTATION AS CONJUNCTIVE THERAPY TO LIFE STYLE CHANGES IN OBESE ADOLESCENTS Marta Ramon-Krauel Received Received
  384-P2 Obesity in ROHHADNET syndrome: does cortisol play a role? Vera van Tellingen Received Received
  387-P2 Biovascular markers in children with Kabuki syndrome Nina Schott Received Received
  388-P2 Phthalate exposure and metabolic parameters in Korean girls Shin-Hye Kim Received Received
  389-P2 Childhood Craniopharyngioma with Hypothalamic Obesity No Long-term Weight Reduction due to Rehabilitation Programs Hermann Mller Received Received
  392-P2 UNALTERED RATIO OF CIRCULATING LEVELS OF GROWTH HORMONE (GH) ISOFORMS AFTER ADMINISTRATION OF DIFFERENT GH PROVOCATIVE TESTS IN A POPULATION OF SHORT STATURE CHILDREN Cristina Meazza Received Received
  393-P2 STUDY OF IGF1 RECEPTOR (IGF1R) GENE IN SMALL FOR GESTATIONAL AGE (SGA) PATIENTS WITH SHORT STATURE TREATED WITH RhGH. Marta Ferrer Received Received
  394-P2 Gene expression profiles in growth hormone deficient (GHD) children relate peak GH levels to circadian clock, chromatin remodelling and WNT signalling pathways Philip Murray Received Received
  395-P2 Growth and growth hormone in Kabuki syndrome Nina Schott Received Received
  396-P2 IGF-II and lipid profile in pediatric obesity: a marker of cardio-metabolic risk? elena inzaghi Received Received
  397-P2 Silver Russell Syndrome (SRS): a cause of partial IGF-I resistance? Marie-Nolle DUFOURG Received Received
  398-P2 The in vitro functional analysis of gene promoter region single nucleotide polymorphisms (SNPs) associated with growth hormone (GH) response in children with GH deficiency Adam Stevens Received Received
  399-P2 IS RETESTING IN GROWTH HORMONE DEFICIENT CHILDREN REALLY USEFUL? Sara Pagani Received Received
  400-P2 Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during Central Precocious Puberty therapy. MARIANA SARTI DE PAULA Received Received
  401-P2 GRB10 knockdown in Zebrafish is associated with decreased weight-to-length ratio without alterations in AKT and ERK activity: a model to study human growth regulation Adam Stevens Received Received
  402-P2 The involvement of the Epidermal Growth Factor Receptor (EGFR) in the successful Growth Hormone (GH) signaling and the role of p21 in the negative regulation of the GH/GHR and EGF/EGFR pathways, in Growth Hormone Transduction Defect (GHTD). Eirini Kostopoulou Received Received
  403-P2 Homozygous carriers of a novel IGFALS mutation are 1.5 SD shorter than heterozygous relatives and tend to have lower bone mineral density Is&305;k Emregl Received Received
  404-P2 The role of beta-TrCP (-TrCP), an E3 ubiquitin ligase, in the signaling of the Growth Hormone (GH) and Epidermal Growth Factor (EGF) pathways in Growth Hormone Transduction Defect (GHTD). Eirini Kostopoulou Received Received
  405-P2 SGA Short Stature Bearing with a Novel Nonsense Mutation (p.W1249X) in the IGF1R Gene Masanobu Fujimoto Received Received
  406-P2 Metabolic Health in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial. Manouk van der Steen Received Received
  407-P2 A Phase 2, six-month, randomized, active-controlled, safety and efficacy study of TransCon hGH compared to daily hGH in children with Growth Hormone Deficiency (GHD) Michael Beckert Received Received
  408-P2 Does skeletal disproportion in children with idiopathic short stature influence response to Growth Hormone (GH) therapy? Cecilia Camacho-Hbner Received Received
  409-P2 THE INFLUENCE OF GROWTH HORMONE THERAPY ON CHEMERIN CONCENTRATION, BODY MASS AND SELECTED PARAMETERS OF CARBOHYDRATE METABOLISM IN PREPUBERTAL NON-OBESE CHILDREN WITH GROWTH HORMONE DEFICIENCY Agnieszka Rudzka-Kocjan Received Received
  410-P2 Response to growth hormone treatment in the very young with growth hormone deficiency Semra etinkaya Received Received
  411-P2 ESTIMATION OF ADIPSIN, OMENTIN AND VASPIN CONCENTRATION IN PREPUBERTAL CHILDREN WITH GROWTH HORMONE DEFICIENCY BEFORE AND AFTER 6 MONTHS OF GROWTH HORMONE TREATMENT Agnieszka Rudzka-Kocjan Received Received
  412-P2 Final Height and Safety Outcomes in Growth Hormone (GH)-Treated Children Born Small for Gestational Age (SGA): Experience from the Prospective GeNeSIS Observational Study Christopher Child Received Received
  413-P2 Results up to January 2015 from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope in children requiring growth hormone treatment Markus Zabransky Received Received
  415-P2 The Pharmacokinetics and Pharmacodynamics of TV-1106, a Once Weekly Growth Hormone Supplement: Results from a Phase 2 Study of TV-1106 in Adults with Growth Hormone Deficiency Pippa Loupe Received Received
  417-P2 GH THERAPY IN SKELETAL DYSPLASIAS: FINAL HEIGHT (FH) DATA. LAURA MAZZANTI Received Received
  418-P2 Random forest classification predicts response to growth hormone (GH) in GH deficient children using baseline clinical parameters and genetic markers Adam Stevens Received Received
  419-P2 Safety evaluation of long-term recombinant growth hormone treatment in childhood: interim analysis of the NordiNet International Outcome Study Michael Maddalena Received Received
  420-P2 Hypoglycaemic adverse events reported in children enrolled in the European Increlex Growth Forum Database (EU-IGFD) in Europe (5-year interim data) Joachim Worlfle Received Received
  421-P2 Application of neural networks for final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH Joanna Smyczynska Received Received
  423-P2 The accuracy of bioelectrical impedance analysis (BIA) to detect the body composition changes in adolescents with severe GHD during transition Julian Ziegler Received Received
  424-P2 Timing of GH peak in provocation tests is important in predicting the effectiveness of treatment with rhGH in prepubertal children with GHD Athanasios Christoforidis Received Received
  426-P2 The ALS dose matters? Response to human growth hormone treatment in patients with acid-labile subunit deficiency Susanne Bechtold Received Received
  427-P2 rhGH replacement therapy ameliorates body composition substantially but has no effect in the quality of life in adolescents with GH deficiency A cross-sectional study Charikleia Stefanaki Received Received
  428-P2 Evaluation of the effect of growth hormone treatment on insulin resistance and cardiovascular tissue Feyza Darendeliler Received Received
  429-P2 EFFECTIVENESS OF RECOMBINANT IGF-I TREATMENT IN A PATIENT WITH ISOLATED GH IA DEFICIT PRODUCER OF ANTI-GH ANTIBODIES. INES PORCAR Received Received
  430-P2 Analysis of CD133CD45 hematopoietic progenitor/stem cells and CD133/CD45- very small embryonic-like stem cells in children with growth hormone deficiency subjected to growth hormone (GH) therapy Beata Sawicka Received Received
  431-P2 Effectiveness of rhIGF-I treatment in a girl with Leprechaunism Clemens Kamrath Received Received
  432-P2 A perioperative changes of Anti-Mullerian Hormone (AMH) and E2 in a patient with SCTAT Aya Shimada Received Received
  435-P2 Clinical criteria remain paramount for the diagnosis of polycystic ovary syndrome in the adolescent age group Liat de Vries Received Received
  436-P2 Gonadal and sexual dysfunction in childhood cancer survivors Ju Young Yoon Received Received
  439-P2 Markers of fertility and quality of life in adolescents with chronic endocrine diseases at the time of transition from paediatric to adult care Janna Mittnacht Received Received
  440-P2 A NOVEL ANDROGEN RECEPTOR GENE MUTATION IN TWO PATIENTS WITH A 46,XY DISORDER OF SEX DEVELOPMENT María Sanz Fernández Received Received
  441-P2 The effect and pharmacokinetics of percutaneous administration of dihydrotestosterone gel in Chinese Children with microphallus jun zhang Received Received
  442-P2 DIFERENTIAL REGULATION OF SERUM SEX HORMONE BINDING GLOBULING IN POLYCYSTIC OVARIAN SYNDROME GIRLS IN RELATION TO WEIGHT Marta Murillo Received Received
  443-P2 Usefulness of 3D ultrasonography for assessment of the morphology of the ovary in adolescents with hyperandrogenism Iwona Ben-Skowronek Received Received
  444-P2 An unusual cause of primary amenorrhoea suggested by the urine steroid profile Noemi Auxiliadora Fuentes-Bolaños Received Received
  445-P2 The late effects after the hematopoietic stem cells transplantation (HSCT) for patients with non-neoplastic disease Akito Sutani Received Received
  446-P2 Body mass index negatively correlates with growth hormone response to GH provocation testing. Ioannis- Anargyros Vasilakis Received Received
  447-P2 SHOX mutation spectrum in an unbiased cohort of 585 patients referred for Leri-Weill dyschondrosteosis or idiopathic short stature. Alberta Belinchon Martinez Received Received
  449-P2 Risk for non-alcoholic fatty liver disease in young adults born preterm Laura Breij Received Received
  450-P2 Pharmacokinetics and Efficacy of a long-acting human growth hormone with Fc fusion protein SU JIN KIM Received Received
  452-P2 Skeletal Dysplasia with Short Stature and a Larsen-like Phenotype due to a Homozygous Mutation in B3GAT3 Elisabeth Steichen-Gersdorf Received Received
  453-P2 Cross-sectional and longitudinal follow-up of changes in glucose metabolism in prepubertal growth-hormone (GH)-treated SGA-patients: results of an unicentric study. Carmen Sydlik Received Received
  454-P2 Growth Pattern in children affected of Lowe Syndrome. Descriptive multicenter international study: Preliminary data Larisa Suarez-Ortega Received Received
  455-P2 Effect of aromatase inhibitor treatment during adolescence on the final adult height in males with idiopathic short stature Yan-hong Li Received Received
  457-P2 Low Plasma Ghrelin Levels in Children with Severe Protein Energy Malnutrition Rakesh Kumar Received Received
  458-P2 Sleep apneas in Silver Russell syndrome : A constant finding Irène Netchine Received Received
  459-P2 Heterozygous NPR2 mutations cause disproportionate short stature, similar to Léri-Weill dyschondrosteosis Alfonso Hisado Oliva Received Received
  460-P2 INDIVIDUALS WITH COWS MILK ALLERGY ARE AT RISK FOR NOT REACHING THEIR GROWTH POTENTIAL Tali Sinai Received Received
  461-P2 French growth reference charts should be updated Stoupa Athanasia Received Received
  462-P2 Advanced bone age and accelerated dental development associated with elevated retinoic acid levels and haploinsufficiency of CYP26A1 and CYP26C1 Ola Nilsson Received Received
  463-P2 Recurrent IGFALS gene mutations p.E35Gfs17 and p.L409F;A475V: hot spot or founder effect? Horacio Domené Received Received
  464-P2 INFANT WITH PHENOTYPE SUGGESTIVE OF SILVER-RUSSELL SYNDROME AND STUDY OF NORMAL METHYLATION: CONSIDER 12Q14.3Q15 MICRODELETION SYNDROME. Blanca Lidia Galo Received Received
  465-P2 Making adult height prediction complete: Forecasting the age of the growth spurt and the height & velocity trajectories until adulthood David Martin Received Received
  467-P2 Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease Gnl Catli Received Received
  468-P2 Novel heterozygous ACAN mutations in short stature: expanding the clinical spectrum LUCIA SENTCHORDI Received Received
  469-P2 Major improvement in parental perception of their childrens height-specific quality of life after one year of GH treatment - our experience with the QoLiSSY (Quality of Life in Short Stature Youth) questionnaire. Laura G. González Briceño Received Received
  470-P2 HYPOMETHYLATION WITHIN THE IMPRINTED DLK1 - DIO3 DOMAIN : A POTENTIAL REGULATORY MECHANISM OF PRE AND POSTNATAL GROWTH Anna Prats-Puig Received Received
  473-P2 The pubertal gain in height is inversely related to BMI in childhood Anton Holmgren Received Received
  474-P2 Growth curves for achondroplasia - height, weight, BMI and head circumference Andrea Merker Received Received
  475-P2 Growth hormone deficiency and pituitary dysgenesis in a girl with microdeletion 2q31.1 Elke Hammer Received Received
  476-P2 One Year Screening Program for Stature Deviations - Strategy and Outcome Galina Yordanova Received Received
  477-P2 BASIC: Bone Age Study In Children Charlotte Elder Received Received
  478-P2 Comparison of the Turkish Growth Standards with the WHO standards ZEHRA YAVAS ABALI Received Received
  479-P2 Moya Moya syndrome in a patient with growth hormone deficiency and hypergonadotropic hypogonadism: to treat or not to treat with growth hormone therapy? Laura G. González Briceño Received Received
  480-P2 In vitro functional characterization of IGFALS gene variants found in ALS deficient or idiopathic short stature (ISS) children Horacio Domené Received Received
  481-P2 KLINEFELTER SYNDROME WITH SHORT STATURE AND MICROCEPHALY: AN UNUSUAL COMBINATION Blanca Lidia Galo Received Received
  482-P2 Childhood Growth of Boys with Congenital Hypogonadotropic Hypogonadism Tero Varimo Received Received
  483-P2 HYPERMETHYLATION AT THE IMPRINTED C19MC microRNA CLUSTER: A NEW LINK BETWEEN MATERNAL METABOLISM AND INFANTS GROWTH. Anna Prats-Puig Received Received
  484-P2 Challenged diagnosis on hypoglycemia: Hirata Disease X Factitious Hypoglycemia TIAGO JERONIMO DOS SANTOS Received Received
  486-P2 Transient Hyperinsulinaemic Hypoglycaemia in Association with a Novel ABCC8 Mutation: Expanding the Clinical Phenotypes Ved Bhushan Arya Received Received
  487-P2 Congenital hyperinsulinism in Ukraine Globa Eugenia Received Received
  488-P2 Unexplained altered states of consciousness in a girl Stefanie Graf Received Received
  489-P2 The Effectiveness of Sirolimus in a Newborn with Hyperinsulinemic Hypoglycemia Belma Haliloglu Received Received
  490-P2 CONGENITAL HYPERINSULINISM CAUSED BY A COMBINATION OF NOVEL HETEROZYGOUS ABCC8 AND KCNJ11 MUTATIONS Klara Rozenkova Received Received
  491-P2 FUNCTIONAL ANALYSIS OF NOVEL ABCC8 MUTATIONS FOUND IN CZECH PATIENTS WITH CONGENITAL HYPERINSULINISM Klara Rozenkova Received Received
  492-P2 Syndromic hypoketotic, hypoinsulinemic hypoglycaemia due to a mosaic activating phosphatidylinositol 3-kinase (PI3K) mutation Sebastian Kummer Received Received
  493-P2 Long Acting Somatostatin Analogue (Lanreotide) therapy in Congenital Hyperinsulinism - Pharmacokinetics and long term follow-up study Pratik Shah Received Received
  494-P2 Congenital Hyperinsulinism in association with Poland Syndrome and Chromosome 10p11-p13 duplication Dinesh Giri Received Received
  495-P2 Rapid Biochemical Evaluation Aids Timely Management of Congenital Hyperinsulinism Julie Park Received Received
  496-P2 Serial 3-dimensional ultrasonographic evaluation of foetal adrenal volumes in the 2nd and 3rd trimester of pregnancy characterises human adrenal development in utero. Nerma Baftic Received Received
  497-P2 Genetic variation in the FSH signalling pathway affects female reproductive hormones during infancy Louise Scheutz Henriksen Received Received
  498-P2 Longitudinal comparison of inhibin B and AMH levels, and testicular volumes between preterm and full-term infant boys Tanja Kuiri-Hnninen Received Received
  499-P2 Postnatal catch-down growth is not associated with disturbances in metabolic parameters in large-for-gestational-age infants at the age of eight years Julia Peters Received Received
  500-P2 Birth incidence of Prader-Willi syndrome in France Céline Bar Received Received
  501-P2 Variation of Environmental Chemicals Measured in Serum During Pregnancy Maria Assens Received Received
  502-P2 Auxological parameters, endocrine growth factors and insulin resistance from birth to 12 months of life in children born small for gestational age (SGA) Laura Guazzarotti Received Received
  503-P2 SERUM FETUIN-A LEVEL FOR DIAGNOSIS HEPATIC STEATOSIS IN CHILDEREN WITH TYPE 1 DIABETES MELLITUS Selim Kurtoglu Received Received
  504-P2 Association of Dll4 levels and VEGFR-1, VEGFR-2 in mice model of oxygen-induced retinopathy Wangkai Liu Received Received
  505-P2 EVALUATION OF THYROID FUNCTION IN PRETERM NEWBORNS OF 24-30 WEEKS OF GESTATION ARIADNA CAMPOS Received Received
  507-P2 Fanconi Anemia Endocrine Abnormalities - case report Liliana Abreu Received Received
  508-P2 The IGSF-1 Deficiency Syndrome: An Unusual Case Javier Aisenberg Received Received
  509-P2 Survival, Hypothalamic Obesity, and Neuropsychological/Psychosocial Status afterChildhood-onset Craniopharyngioma: Newly reported Long-term Outcomes Anthe Suzan Sterkenburg Received Received
  510-P2 CHRONIC INAPPROPRIATE ANTIDIURESIS IN CHILDHOOD: EXPERIENCE WITH TOLVAPTAN Claudia Piona Received Received
  511-P2 Pituitary hormone secretion profiles in IGSF1 deficiency syndrome Sjoerd Joustra Received Received
  513-P2 A novel mutation within the AVP gene in an 18-year-old male patient with Kallmann syndrome and combined pituitary hormone deficiency Won Bok Choi Received Received
  514-P2 Hydrocephalus and Hypothalamic Involvement in Pediatric Patients with Craniopharyngioma or Cysts of Rathkes Pouch: Impact on Long-term Prognosis Anna Maria Daubenbchel Received Received
  515-P2 Contrasting central diabetes insipidus due to preproAVP mutations: earlier onset of symptoms in recessive than in dominant forms Bourdet Karine Received Received
  516-P2 ENDOCRINE DISORDERS IN CHILDREN WITH OPTIC CHIASM GLIOMA Alicia Torralbo-Carmona Received Received
  517-P2 Be aware of congenital panhypopituitarism in children with a family history of polydactyly Idske Kremer Hovinga Received Received
  519-P2 Eating behavior, weight problems and eating disorders in 101 long-term survivors of childhood-onset craniopharyngioma Anika Hoffmann Received Received
  520-P2 Two novel LHX3 mutations in patients with combined pituitary hormone deficiency and sensorineural hearing loss BASSAM BINABBAS Received Received
  521-P2 A novel entity characterized by growth hormone deficiency (GHD) and central precocious puberty (CPP) in two siblings, in the absence of central nervous system (CNS) abnormality Antonis Voutetakis Received Received
  523-P2 Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes Fernanda Correa Received Received
  524-P2 Pulsatile GnRH is superior to hCG in therapeutic efficacy in adolescent boys with hypogonadotropic hypogonadodism Ying Liu Received Received
  525-P2 The lack of MKRN3 gene mutations in patients with idiopathic sporadic GnRH-dependent precocious puberty Beata Wikiera Received Received
  526-P2 Serum AMH levels are lower in healthy boys who develop pubertal gynaecomastia Mikkel G. Mieritz Received Received
  527-P2 Evaluation of final height in girls taking GnRH analogue: Should the age limit for precocious puberty be changed? Dogus Vuralli Received Received
  528-P2 Correlation of clinical phenotype and genotype of Prader-Willi syndrome (PWS) and the deletion of paternal MKRN3 allele in PWS patients with central precocious puberty Jahyang Cho Received Received
  529-P2 Doppler evaluation of the uterine artery for the diagnosis and follow-up of patients with precocious puberty Jeannette Linares Received Received
  530-P2 Nephrogenic Diabetes Insipidus with partial response to ddAVP caused by a novel AVPR2 splice site mutation Ola Nilsson Received Received
  531-P2 Regional Brain Volume and Luteinizing Hormone in Girls with Idiopathic Central Precocious Puberty Eun Young Kim Received Received
  532-P2 Determination of final height in girls with precocious puberty. Which is the most accurate method? Constanza Pinochet Received Received
  533-P2 The relationship between steriod receptors and Aromatase in the Mouse Brain Bertan Yilmaz Received Received
  534-P2 Evaluation of body proportions in children with precocious or delayed puberty Michael Hauschild Received Received
  535-P2 GH Deficiency with Advanced Bone Age: GHRH Receptor mutation detected by exome sequencing associated to non-classical congenital adrenal hyperplasia (CAH) Fernanda Correa Received Received
  536-P2 Ultra-deep next-generation sequencing: a reliable method for the molecular diagnosis of McCune Albright syndrome. Florence Roucher Boulez Received Received
  537-P2 Increased ambulatory blood pressure in adolescents with gender dysphoria treated with gonadotropin- releasing hormone analogues Daniel Klink Received Received
  538-P2 Plasma humanin levels during normal childhood and puberty. Study of possible correlations with sex, age, and insulin levels. Marta Ciaccio Received Received
  539-P2 GnRH Infusion in Females with Hypogonadotrophic Hypogonadism Analia Freire Received Received
  540-P2 A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene. Anna Grandone Received Received
  543-P2 The Endocrine Response to a Gonadotropin Releasing Hormone (GnRH) Test: Establishing a Reference Interval in Healthy Girls below 6 Years of Age Niels Birkebk Received Received
  544-P2 Increasing body mass index is associated with lower luteinizing hormone levels in girls with central precocious puberty at the early pubertal stage. Hae Sang Lee Received Received
  545-P2 Change of Growth Pattern and Bone Mineral Density in Ovariectomized Female Rats According to Estrogen Dosage Byung Ho Kang Received Received
  546-P2 Gynecomastia with precocious onset in Peutz-Jeghers Syndrome: managing the aromatase overexpression Joana Simes Pereira Received Received
  547-P2 The impact of growth hormone (GH) therapy combined with estrogens on blood pressure (BP), cardiac left ventricular (LV) dimensions and lipid metabolism in pubertal girls with Turners syndrome (TS). Tatiana Shiryaeva Received Received
  548-P2 Sensitivity of measured parental height and target range in the diagnosis of Turner syndrome Yasmine Ouarezki Received Received
  549-P2 Balance control in children and adolescent girls with Turner syndrome. Bruno LEHEUP Received Received
  550-P2 SHORT STATURE WITH NEURODEVELOPMENTAL DELAY IN FAMILIAL VARIANT TURNER SYNDROME Madhurima Chetan Received Received
  551-P2 Diagnostic significance of serum concentrations of osteoprotegerin and proinflammatory cytokine IL-1 in children with autoimmune thyroid disease. Marek Niedziela Received Received
  552-P2 Even in the era of congenital hypothyroidism screening mild and subclinical sensorineural hearing loss remains a relatively common complication of severe congenital hypothyroidism Malgorzata Wasniewska Received Received
  553-P2 Efficacy of supplemental Liothyronine for patients with congenital hypothyroidism and pituitary resistance to thyroid hormone Laura Paone Received Received
  554-P2 Hypoceruloplasminemia as a marker of severe hypothyroidism Mariella Valenzise Received Received
  555-P2 PITUITARY RESISTANCE TO EXOGENOUS LEVOTHYROXINE IN HUMANS Nerea Lacámara Received Received
  557-P2 Potentially excessive levothyroxine doses in cases of congenital hypothyroidism with eutopic thyroid gland Hidetoshi Satoh Received Received
  558-P2 Objective versus subjective measurement of thyroid volume by ultrasound in infants referred with TSH elevation on newborn screening Chourouk Mansour Received Received
  559-P2 Central or Primary Hypothyroidism? How to Differentiate in Patients with low T4 but mildly elevated TSH levels Serap Turan Received Received
  561-P2 Analysis of chosen polymorphisms rs5742909 C/T - CTLA4, rs7522061 C/T FCRL3, rs7138803 A/G - FAIM2 in pathogenesis of autoimmune thyroid diseases in children. Ewa Jakubowska Received Received
  562-P2 THYROID DYSFUNCTION IS ASOCIATED WITH BIOCHEMICAL MARKERS OF NON ALCOHOLIC FATTY LIVER DISEASE (NAFLD) IN PEDIATRIC POPULATION Carolina Loureiro Received Received
  563-P2 Nonautoimmune neonatal hyperthyroidism due to A633G mutation in the thyrotropin receptor gene In Ah Jung Received Received
  565-P2 Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimotos thyroiditis to Graves disease and beyond Malgorzata Wasniewska Received Received
  566-P2 Analysis of B regulatory cells with phenotype CD19CD24hiCD27IL-10 and CD19IL-10 in the peripheral blood of children with Graves disease and Hashimotos thyroiditis Artur Bossowski Received Received
  567-P2 Case Report: Resistance of Thyroid Hormone due to a novel Thyroid Hormone Receptor -Gene Mutation meltem TAYFUN Received Received
  570-P2 GOITROUS HYPOTHYROIDISM OF PUBERTAL ONSET CAUSED BY A NOVEL MUTATION IN DEHAL1 GENE. Esther Schulz Received Received
  572-P2 Mutational analysis of TSH receptor and the clinical characteristics of congenital hypothyroidism Jeesuk Yu Received Received
  574-P2 Three year follow-up of children with abnormal newborn screening results for congenital hypothyroidism: Who needs treatment and who needs permanent treatment? Min Jae Kang Received Received
  575-P2 Attention Deficit (AD) and Sluggish Cognitive Tempo (SCT) symptoms in Congenital Hypothyroidism (CH): results from a case-control study. Ida DAcunzo Received Received
  577-P2 Osteoprotegerin and free T4 levels in subclinical hypothyroidism of childhood Aristeidis Giannakopoulos Received Received
  578-P2 Cryptorchidism is commonly observed in Allan Herndon Dudley syndrome Noriyuki Namba Received Received
  579-P2 Co-existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis; A Single-Center Study senay savas erdeve Received Received
  580-P2 The diagnostic, treatment and follow-up features of childhood thyroid malignancies-A preliminary report Ediz Yesilkaya Received Received
  581-P3 New mutation causing systemic Pseudohypoaldosteronism Stefania Pedicelli Received Received
  582-P3 Rapid Molecular Diagnosis of CAH by Strip Hybridization Assay in DEMPU Amany Ibrahim Received Received
  583-P3 Insufficient mineralocorticoid replacement as a predictor factor for the TART in boys with congenital adrenal hyperplasia Igor Chugunov Received Received
  584-P3 CYP11B1 Gene Mutations in Patients with Congenital Adrenal Hyperplasia in Turkey Firdevs Bas Received Received
  585-P3 Living with adrenal hyperplasia for children in primary school between 6 and 11 years.Educational innovation and design of a learning tool for therapeutic education Catherine PIENKOWSKI Received Received
  587-P3 ADRENAL ATROPHY SECONDARY TO INAPPROPRIATE ORAL ADMINISTRATION OF EXOGENOUS STEROID PRESENTING WITH HYPERCALCEMIA Suna Kilinc Received Received
  588-P3 CASE REPORT: HYPOTHYROIDISM AND ACTH-DEFICIENCY CAUSED BY TBX 19 MUTATION:COINCIDENCE OR PATHOGENETIC CORRELATION? Esther Schulz Received Received
  589-P3 Deletion Mapping in Xp21 for a family With Complex Glycerol Kinase Deficiency Using Array-based comparative genomic hybridization Zhangqian Zheng Received Received
  590-P3 Characterization of Ovarian Adrenal Rest Tumors in Children and Adolescent Females with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency Zhe Su Received Received
  591-P3 Pseudohypoaldosteronism Subtle presentations with critical electrolyte imbalances Experiences from one hospital Caroline Ponmani Received Received
  592-P3 Atypical prednisone-metabolism: Pharmacological studies in a boy with classical adrenal hyperplasia and suspected malcompliance Hess Melanie Received Received
  593-P3 CYP21A2 gene mutations analysis in 21 Chinese patients with salt-wasting form of congenital adrenal hyperplasia Hui Yao Received Received
  594-P3 X-Linked Adrenoleucodystrophy (X-ALD) presenting as Addisons disease in childhood: a case report. Antonella Meloni Received Received
  595-P3 Three Siblings with Corticosterone Methyloxidase Deficiency Type 2 due to c.1175TC mutation a Novel c.788TA Mutation in CYP11B2 gene Evliyaoglu Olcay Received Received
  596-P3 Transient pseudohypoaldosteronism as a complication of infected obstructive uropathy in infancy, a case series. Alexandra Rodrigues Da Costa Received Received
  597-P3 Generalized glucocorticoid resistance in an adolescent girl with severe hyperandrogenia without mutations in NR3C1 gene. Nadezda Makazan Received Received
  598-P3 Remission with Cabergolin with Recurrent hypercortisolism after pituitary surgery in Cushings Disease &304;lkin Majidov Received Received
  599-P3 Phaeochromocytoma in placental mesenchymal dysplasia: who should we screen and for how long? Mary White Received Received
  600-P3 A DOUBLE DOSE OF TRIPLES V. SRINAGESH Received Received
  601-P3 Central cortisol deficiency (isolated ACTH deficiency)in a child. Fawziya Alyafei Received Received
  602-P3 THE FIRST CASE OF PRIMARY GENERALIZED GLUCOCORTICOID RESISTANCE IN SERBIA IN AN 8 YEAR OLD BOY WITH G679S MUTATION OF THE NR3C1 GENE Katarina Mitrovic Received Received
  603-P3 A CASE OF PHEOCHROMOCYTOMA DIAGNOSED AS ADRENAL INCIDENTALOMA Dogus Vuralli Received Received
  604-P3 Severe high blood pressure with renal failure in a neglected case of 11-hydroxylase deficient congenital adrenal hyperplasia (11-OH CAH) BELCEANU ALINA Received Received
  605-P3 Delayed diagnosis of salt wasting congenital adrenal hyperplasia, without complications of cortisol deficiency: a case report Karijn Pijnenburg-Kleizen Received Received
  606-P3 Familial Hyperaldosteronism Type I in an infant without hypertension: how important could be the early treatment with hydrocortisone? Alejandro Gregorio Martinez-Aguayo Received Received
  608-P3 A PROSPECTIVE EVALUATION OF ANTHROPOMETRIC AND METABOLIC PROFILE IN PREMATURE ADRENARCHE PATIENTS glcan seymen karabulut Received Received
  610-P3 Development of a patient with severe pseudohypoaldosteronism due to mutation in the alpha subunit of ENaC Erwin Lankes Received Received
  611-P3 Methodological considerations into the approach for genetic diagnostics of CAH in a girl with SW form and relatively higher needs of mineralcorticoids Ganka Dineva Received Received
  612-P3 11-hydroxylase deficiency: Twenty years follow-up Didem Helvacioglu Received Received
  613-P3 Near-final height outcome of congenital adrenal hyperplasia (CAH) due to classic 21-hydroxylase deficiency(21OHD) in 55 Chinese patients Ma Huamei Received Received
  614-P3 Late diagnosis of childhood adrenal insufficiency and hypogonadotropic hypogonadism due to DAX 1 gene mutation maria karantza Received Received
  615-P3 Paraaortical paragangliomas as incidental findings in a female adolescent. Eleni Kotanidou Received Received
  616-P3 Nephrotic syndrome developing in a girl with classic 21-hydroxylase deficiency---first report Huamei Ma Received Received
  617-P3 Conservative treatment of neonatal Cushings syndrome in McCune Albright syndrome, a 2 year follow-up Nancy Nieuwaal, van Received Received
  618-P3 A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia:Molecular genetics report from Saudi Arabia Sarar Mohamed Received Received
  619-P3 Adrenal cortex dysfunction as a consequence of chronic therapies other than oral steroid therapy cases presentation. Izabela Rogozinska Received Received
  620-P3 A RARE CAUSE OF HYPERTENSION: PSEUDOPHEOCHROMOCYTOMA Nihal Hatipoglu Received Received
  621-P3 A Case of X-Linked Adrenal Hypoplasia Congenita; Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency and Duchenne Muscular Dystrophy Bilgin Yuksel Received Received
  622-P3 Prenatal treatment of Congenital Adrenal Hyperplasia (CAH): A survey of Paediatric Endocrinologist.Ethical group of Sociedad Española de Endocrinología Pediátrica (SEEP) Maria J Chueca Guindulain Received Received
  623-P3 A case of ACTH resistance with generalized hyperpigmentation at birth Takako SASAKI Received Received
  624-P3 Clinical and genotypic characterization of simple virilizing forms of congenital adrenal hyperplasia Rita Cardoso Received Received
  625-P3 ?Reexpansion of testicular tissue after testis-sparing surgery in an adolescent Emine Ayca Cimbek Received Received
  626-P3 Exogenous Cushings syndrome due to misuse of topical corticosteroid therapy Maria Korpal- Szczyrska Received Received
  627-P3 Familial Glucocorticoid Deficiency A case report Navoda Atapattu Received Received
  628-P3 Assessment of ovarian function and reserve based on hormonal parameters, ovarian volume, and follicle count in euthyroid girls with Hashimoto thyroiditis Ozgur Pirgon Received Received
  629-P3 Early-onset type 1 diabetes and multiorgan autoimmunity in a girl with partial monosomy 2q and trisomy 10p Carla Bizzarri Received Received
  630-P3 CTLA4 A49G and C60T genetic polymorphism in Croatian children and young adults with autoimmune thyroid disease Natasa Rojnic Putarek Received Received
  631-P3 Oocyte cryopreservation in a patient with premature ovarian failure due to autoimmune polyendocrine syndrome type 2. claudia balsamo Received Received
  632-P3 Thyroid function and autoimmunity in children with newly diagnosed type 1 diabetes mellitus. El&380;bieta Niechcia&322; Received Received
  633-P3 HYPERCALCAEMIA AS AN INDICATION OF ADRENAL INSUFFICIENCY IN A PATIENT WITH AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY (APECED) ELLI ANAGNOSTOU Received Received
  635-P3 Radiologic appearance is important for diagnosis of autoimmune hypophysitis Erkan Sar&305; Received Received
  637-P3 About a case of Basedow-Graves disease in a infantM.A.Bassaid , K.Bouriche , A.S.Bendeddouche PédiatricsA.Medjahdi, N.Berber Nuclear Medicine Mohammed El-amin Bassaid Received Received
  638-P3 THE AUTOIMMUNE POLYENDOCRINOPATHIES in children and Adolescents NORA SOUMEYA FEDALA Received Received
  639-P3 Is serum serotonin involved in the bone loss of young females with anorexia nervosa ? maimoun laurent Received Received
  640-P3 Cranial MR Spectrometry Findings of Patients Aged 10-15 years with Diagnosis of Rickets Murat Dogan Received Received
  641-P3 Evaluation of bone geometry, quality and bone markers in children with type 1 diabetes Silvia Longhi Received Received
  642-P3 Comparison of treatment alternatives for hypercalcemia due to vitamin D intoxication in children Korcan Demir Received Received
  643-P3 Influence of birth weight and total body less head bone mineral contents in 10-18 Korean adolescents: Results from the Korea National Health and Nutrition Examination Surveys (KNHANES) 2008 - 2010. WONKYOUNG CHO Received Received
  644-P3 Clinical and molecular characterization of patients with pseudohypoparathyroidism Eungu Kang Received Received
  645-P3 Long term effects of bisphosphonate treatment in a case with infantile onset severe form of juvenile Pagets disease E. Nazli Gonc Received Received
  646-P3 Diagnosis and management of Gorham-Stout disease: a protocol proposal Natascia Di Iorgi Received Received
  647-P3 Vitamin D dependent rickets type 1A with genetic analysis in 3 Chinese children Wenjing LI Received Received
  648-P3 A novel mutation in CYP24A1 gene in an infant with severe hypercalcemia and unique neurological presentation Yael Levy-Shraga Received Received
  649-P3 CONTINUOUS 1-34 rhPTH THERAPY IN A GIRL WITH A PTH-GENE DEFECT Diana-Alexandra Ertl Received Received
  650-P3 PREVALENCE OF VITAMIN D DEFICIENCY IN SICKLE CELL ANEMIC CHILDREN IN JOS, NIGERIA Ibrahim Abok Received Received
  651-P3 VITAMIN D LEVEL AND VITAMIN D RECEPTOR DNA IN CHILDREN WITH DIABETES MELLITUS STUDYING SEQUENCE ANALYSE AND POLIMORPHISM Murat Dogan Received Received
  652-P3 Endocrine function, vitamin D and bone mass status in -thalassemia major. AYA ALTINCIK Received Received
  653-P3 LATE SEQUEL OF MENINGOCOCCEMIA: PRESENTING AS SKELETAL DYSPLASIA glcan seymen karabulut Received Received
  654-P3 LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF-I levels Carlos Martinelli Jr Received Received
  655-P3 A longitudinal, prospective, long-term registry of patients with hypophosphatasia Kristina Kolygo Received Received
  656-P3 Retrospective Evaluation of Patients Diagnosed as Nutritional Rickets: A Single Center Study Meliksah KESK&304;N Received Received
  657-P3 Discrepancy in bone age rating using Tanner-Whitehouse rating and automated bone age determination in a child who was later diagnosed with metaphyseal dysplasia. Niels Holtum Birkebk Received Received
  658-P3 VITAMIN LEVELS IN PREGNANT WOMEN AND IN CORD BLOOD IN NEWBORN IN OUR AREA. PRELIMINARY RESULTS. Maria Ruiz del Campo Received Received
  659-P3 Vitamin D status in Romanian children 0-18 years should we be more careful regarding supplementation? Adela Chirita Emandi Received Received
  660-P3 4 years follow up for 25OHD and iPTH in Vitamin D substituted patients with Diabetes mellitus 1 (DM1): an unicentric prospective study Claudia Weienbacher Received Received
  661-P3 Bone Mineral Density in Prader-Willi females during the transition phase Graziano Grugni Received Received
  662-P3 Seasonal differences in plasma 25-OH vitamin D concentrations in cord blood Sandra Ortigosa Gómez Received Received
  663-P3 Spondyloenchondrodysplasia with immune dysregulation and without neurological involvement: Report of two siblings with ACP5 gene mutation. Ayse Nurcan Cebeci Received Received
  664-P3 Short stature in Osteogenesis Imperfecta is not caused by deficiencies in IGF1 or IGF-BP3 Oliver Semler Received Received
  665-P3 Vitamin D Status in Children in the Western Part of Turkey bayram ozhan Received Received
  666-P3 PARATHYROID ADENOMA SHOULD BE CONSIDERED IN THE MANAGEMENT OF HYPOPHOSPHATEMIC RICKETS Ulku Gul Received Received
  667-P3 NEUROLOGICAL CLINIC DELAYS THE DIAGNOSIS OF PSEUDOHYPOPARATHYROIDISM Maria Teresa Pérez Received Received
  668-P3 TREATMENT OF LIFE THREATENING HYPERCALCEMIA IN TWO INFANTS Didem Helvacioglu Received Received
  669-P3 Comparison of the levels of vitamin D in children in northern Spain (domestic or foreign) Ignacio Diez Received Received
  671-P3 How are we using bisphosphonates in children with secondary osteoporosis in a tertiary centre? Victoria Price Received Received
  672-P3 PSEUDOHYPOPARATHYROIDISM (PHP): clinical heterogeneity illustrated by 3 different cases. Annelies Lemay Received Received
  673-P3 Successful treatment of severe hypercalcemia in an infant with Williams syndrome using a single infusion of pamidronate followed by low calcium diet. Rasha Odeh Received Received
  674-P3 25-Hydroxy Vitamin D levels in patients with chronic diseases on corticosteroid treatment Desislava Yordanova Received Received
  675-P3 PSEUDOHYPOPARATHYROIDISM TYPE 1b, A RARE DIAGNOSIS IN ADOLESCENTS ELLI ANAGNOSTOU Received Received
  676-P3 What Lies Beneath: An enigma of missed opportunities and Calcium problem Dalia Hammouche Received Received
  677-P3 A novel homozygous 6 nucleotide deletion in GLUT2 gene in a FanconiBickel syndrome family farzaneh abbasi Received Received
  678-P3 Final Heigh(FH) in a patient with Fanconi Syndrome(FS) and Growth Hormone Deficiency(GHD) treated with Growth Hormone Maria Cláudia Schmitt-Lobe Received Received
  679-P3 Carpal spasm in hypophosphatemic patients Sang Hyun Lee Received Received
  683-P3 Hypocalcemia by parathyroid dysfunction in children and adolescents Ali el mahdi HADDAM Received Received
  684-P3 VDR Gene Analysis Results of Four Patients With Hereditary1,25-Dihydroxyvitamin DResistant Rickets Esra Deniz Papatya Cak&305;r Received Received
  685-P3 NUTRITIONAL RICKETS IN A BOTTLE-FED TWO MONTHS OLD BABY Maria Hawkins Received Received
  686-P3 A rare reason of hyperinsulinism: Mnchausen Syndrome by Proxy onur ak&305;n Received Received
  687-P3 Correlation of vitamin D levels with glycemic control, total daily insulin dose, BMI and ethnicity in pediatric patients with type 1 diabetes mellitus. Monica Bianco Received Received
  688-P3 Management of children with Type 1 diabetes during illness (sick days): Is there a need for national consensus guideline? Astha Soni Received Received
  689-P3 Incretin secretion was not impaired in obese Korean children and adolescents with type 2 diabetes SO HYUN PARK Received Received
  690-P3 NEONATAL DIABETES MELLITUS: CLINICAL FEATURE AND OUTCOME Can Thi Bich Ngoc Received Received
  691-P3 Acute kidney injury as a severe complication of diabetic ketoacidosis Alagusutha Jeyaraman Received Received
  692-P3 Body mass index in children and young people with Type 1 diabetes in England and Wales Naomi Holman Received Received
  693-P3 Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study Philippe Lysy Received Received
  694-P3 ELASTARGENE 3C HELPS TO IMPROVE GLYCATED HAEMOGLOBIN IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES USING INSULIN PUMP THERAPY. Andrea Scaramuzza Received Received
  695-P3 Intraosseous infusion: sometimes the only way to treat severe diabetic ketoacidosis Francesco Gallo Received Received
  696-P3 Does the frequency of hypoglycemia influence attention in children with type 1 diabetes? Michael Wurm Received Received
  697-P3 Recurrent ketosis after prolonged exercise in type 1 diabetes the need for glycogen replacement strategies. Case report Mirjam van Albada Received Received
  698-P3 Adherence to Diabetic Ketoacidosis Management Protocol: A Paediatric Center Experience Joanie Barbe Received Received
  699-P3 Continuous intersticial glucose monitoring in early detection of glucose tolerance abnormalities in adolescents with cystic fibrosis. Jacobo Perez Received Received
  700-P3 Health Related Quality of Life in children and adolescents with Type 1 Diabetes Mellitus in Spain: Results from the CHRYSTAL Study. Renata Villoro Received Received
  701-P3 HBA1C RATHER THAN BMI, LIFESTYLE AND ADHERENCE TO MEDITERRANEAN DIET IS THE MAJOR DETERMINANT OF TRIGLYCERIDE/HDL CHOLESTEROL RATIO IN ADOLESCENTS WITH TYPE-1 DIABETES (T1D) STEFANO ZUCCHINI Received Received
  702-P3 Non-HDL cholesterol in diabetic children: Treatment recommendations considering glycemic control, BMI, age, gender, and generally accepted cut points Karl Otfried Schwab Received Received
  703-P3 A 1 year follow up study to evaluate efficacy and compliance of continuous glucose monitoring (CGM) in children with Type 1 Diabetes Mellitus (T1DM) Astha Soni Received Received
  704-P3 Diabetic ketoacidosis treatment: experience from a pediatric tertiary centre (2004-2014) Joana Serra-Caetano Received Received
  705-P3 Treatment of dyslipidemia in children and adolescents with diabetes mellitus type 1 Mariel Borgerink Received Received
  706-P3 Hearing changes in children and adolescents with type 1 diabetes mellitus Young-Jun Rhie Received Received
  707-P3 A novel genetic mutation in a Turkish family with GCK-MODY SELIN ELMAOGULLARI Received Received
  709-P3 Elevated HbA1c and cardiometabolic risk factors in Korean children and adolescents: Data from the Korean National Health and Nutrition Examination Survey, 2011-2012 Jieun Lee Received Received
  710-P3 How appropriate are the lenghts of syringe needles used for subcutaneous injections to the children at school age Murat Dogan Received Received
  711-P3 Heterogeneous Presentation of Paediatric Hyperglycaemic Hyperosmolar State A case series Zainaba Mohamed Received Received
  712-P3 A NOVEL COMPOUND HETEROZYGOUS MUTATION IN AN ADOLESCENT WITH INSULIN-DEPENDENT DIABETES: A CASE REPORT OF WOLFRAM SYNDROME Giulio Maltoni Received Received
  713-P3 Sirolimus therapy in an infant with Persistent Hyperinsulinemic Hypoglycemia Yvonne Lim Received Received
  714-P3 Permanent Neonatal Diabetes Mellitus in Beckwith Wiedemann Syndrome: An unusual co-occurrence. Dipesalema Joel Received Received
  715-P3 Prevalence of vascular complications in children with type 1 diabetes in Ireland Elena Hennessy Received Received
  716-P3 Hyperglycaemia during Chemotherapy for Acute Lymphoblastic Leukaemia among Taiwanese Children Meng-Che Tsai Received Received
  717-P3 Seip-Berardinelli syndrome in a patient referred by low weight gain Cristiane Kopacek Received Received
  718-P3 Effect of Reward-Based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus gonul catli Received Received
  719-P3 Fanconi-Bickel syndrome due to a Novel SLC2A2 Mutation Presenting with Transient Neonatal Diabetes Selin Elmaogullari Received Received
  721-P3 GAD antibodies negative type 1 diabetes and Dravet syndrome Sara Ciccone Received Received
  722-P3 Social risk assessment in children with type 1 diabetes mellitus to plan medical and social care Anna Karpushkina Received Received
  724-P3 Study of Adiponectin Level in Diabetic Adolescent Girls in Relation to Glycemic Control and Complication of Diabetes soha eldayem Received Received
  725-P3 Frequent and prolonged daytime hypoglycemia in diabetic children detected by continuous glucose monitoring (cgms): a problem of hypoglycemia unawareness? Sara Bachmann Received Received
  726-P3 NEONATAL DIABETES MELLITUS DUE TO INSULIN GENE MUTATION Can Thi Bich Ngoc Received Received
  727-P3 SINGLE CENTRE EXPERIENCE OF NEONATAL DIABETES V.SRI NAGESH Received Received
  728-P3 Assessment of the effect of the diagnosis of T1DM in the nutritional habits of unaffected family members Athanasios Christoforidis Received Received
  729-P3 LIFESTYLE AND METABOLIC CONTROL IN ADOLESCENTS WITH TYPE 1 DIABETES (T1D) GRACIA M. LOU-FRANCÉS Received Received
  730-P3 cells functional exhaustion at Type 1 Diabetes onset may lead to early microvascular complications Nektaria Papadopoulou Received Received
  731-P3 Influence of pancreatic autoinmunity in the onset and progression of diabetes in pediatric population Yoko Patricia Oyakawa Barcelli Received Received
  732-P3 Severe insulin resistance and dyslipidaemia with unremarkable fat distribution in an adolescent girl due to mutation in the PPARG gene (Familial partial lipodystrophy type 3) Carsten Ding Received Received
  733-P3 Use of Smartphone, a Cellular Glucometer and Social Media App in the Management of Type 1 DM in the Adolescent Population: The Future of Diabetes Care Steven Ghanny Received Received
  734-P3 A boy with Wolfram syndrome Ho-chung YAU Received Received
  735-P3 Cardiovascular risk factors in children and adolescents with type 1diabetes Carla Ferreira Received Received
  736-P3 Megaloblastic anemia and diabetes in a young girl Anissa Messaaoui Received Received
  737-P3 Glycaemic control in children aged with Type 1 diabetes in Malta. Formosa Nancy Received Received
  739-P3 Assessment of Quality of life in adolescents with type 1 diabetes; A pilot study Noha Musa Received Received
  740-P3 MODY3 early identification and diagnosis Zilberman Lyubov Received Received
  741-P3 Low fT3 syndrome due to metabolic acidosis/ketoacidosis in Type 1 diabetes mellitus (type 1 DM) Heinrich Schmidt Received Received
  742-P3 Coping styles of adolescents with type 1 diabetes and their parents: Association with metabolic control and disease duration. Feneli Karachaliou Received Received
  744-P3 Transition during adolescence, is there room to improve? Sinead Glackin Received Received
  745-P3 Vitamin D status in Egyptian children with T1D and the role of Vitamin D replacement on glycemic control Noha Musa Received Received
  746-P3 RESIDUAL C-PEPTIDE IN PAEDIATRIC PATIENTS WITH TIPE 1 DIABETES Maria Martin-Frias Received Received
  747-P3 A novel nonsense mutation in the WFS1 gene causes the wolfram syndrome Shahab Noorian Received Received
  748-P3 Health Literacy of Caregivers of Children with Type 1 Diabetes: A Pilot Study on Impact on Glycemic Control in an Arabic-speaking Population Dalia Al-Abdulrazzaq Received Received
  751-P3 FASTING THE HOLY MONTH OF RAMADAN IN OLDER CHILDREN AND ADOLESCENCE WITH TYPE 1 DIABETES IN KUWAIT mohamed kholoud Received Received
  752-P3 The long-term insulin management with premixed insulin in neonates and infants with diabetes Hakan Dneray Received Received
  754-P3 Thyroid function and prevalence of celiac disease in children with T1D in Lithuanian pediatric population Ingrida Stankute Received Received
  755-P3 Severe hypertriglyceridemia in a child with severe diabetic ketoacidosis Glay Karagzel Received Received
  756-P3 Factors Related to Progression to Macroalbuminuria in Type 1 Diabetic Children with microalbuminuria Keun Hee Choi Received Received
  757-P3 ACUTE PAINFUL NEUROPATHY IN A TEENAGER WITH TYPE 1 DIABETES (T1D) AND EATING DISORDERS maria louraki Received Received
  758-P3 A Case of Tacrolimus Related Posttranslated Diabetes Mellitus(PTDM) murat karaoglan Received Received
  759-P3 Short-term use of continuous glucose monitoring system in pediatric patients with type 1 diabetes mellitus and correlation with short-term improvement in glycemic control Monica Bianco Received Received
  760-P3 Neonatal diabetes - the great masquerader Experiences from one hospital Caroline Ponmani Received Received
  762-P3 METABOLIC CONTROL AND GLYCEMIC VARIABILITY IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES IN MULTIPLE DAILY INJECTIONS THERAPY USING AUTOMATED BOLUS CALCULATOR GLUCOMETER Marta Murillo Received Received
  763-P3 Maturity onset diabetes of the young: just think about it Anissa Messaaoui Received Received
  764-P3 THE ROLE OF KCNJ11 GENE IN NEONATAL DIABETES soha eldayem Received Received
  765-P3 A case of DEND (developmental delay, epilepsy, and neonatal diabetes) syndrome with heterozygous KCNJ11 mutation successfully treated with sulfonylurea therapy Ja Hye Kim Received Received
  766-P3 TWO PERMANENT NEONATAL DIABETES MELLITUS CASES DUE TO MUTATION IN ABCC8 GENES IN VIET NAM: CLINICAL FEATURES AND LONG TERM OUTCOME IN TREATING BY SULFONYLUREA (2008-2014) Khanh Phuong Nguyen Received Received
  767-P3 Type 1 diabetes in pediatric patients: demographic and clinical characterization Helena Ferreira Received Received
  768-P3 The missing link in Neonatal Diabetes Irene Pilar Fernandez Viseras Received Received
  769-P3 Cutaneous Manifestations among Type 1 Diabetic Patients in DEMPU Amany Ibrahim Received Received
  770-P3 Particularités du diabete chez les enfants dont lage de révélation est avant 5ans Wafaa Korti Received Received
  771-P3 Evaluation Of Boluses Delivered By Insulin Pump In TYPE1 Diabetes Mellitus Pediatric Patients Snijezana Hasanbegovic Received Received
  773-P3 MAURIAC SYNDROME, A RARE COMPLICATION OF TYPE 1 DIABETES MELLITUS MARÍA JOSÉ RIVERO MARTÍN Received Received
  774-P3 Is autoimmunity on the increase in type 1 Diabetes Mellitus?Presentation of multiple auto-immune disorders at diagnosis of type 1 Diabetes Mellitus Diluxy Elangaratnam Received Received
  775-P3 Type 1 diabetes mellitus and precocios puberty : rare association mimouna bessahraoui Received Received
  776-P3 SCHOOL AGED PRESENTATION OF DIABETES MELLITUS TYPE 1 WITH REPEAT HYPERGLYCEMIA, POSITIVE PANCREATIC AUTOIMMUNITY AND RELATED GENETIC RISKS Ana Dolores Alcalde de Alvaré Received Received
  777-P3 Clinical changes observed AFTER SYSTEM IMPLEMENTATION OF JUNIORSTAR systems in children with Dm1a Ignacio Diez Received Received
  778-P3 Metabolic control in children in northern Spain DM1A with deficit of vitamin D Ignacio Diez Received Received
  779-P3 Effects of Educational Interventions for Children and Adolescents with Type I Diabetes Mellitus Sameh Tawfik Received Received
  780-P3 Clinical findings, endocrine profile and genetic features of 5alpha-reductase-2 deficiency Gianni Russo Received Received
  781-P3 Aromatase deficiency due to novel CYP19A1 mutation in an Egyptian patient with ambiguous genitalia inas Mazen Received Received
  782-P3 The time of first presentation at the department of paediatric endocrinology of patients with 46,XY DSD. Zofia Kolesinska Received Received
  784-P3 A cross-sectional growth reference and chart of stretched penile length for Japanese boys aged 07 years: Ethnic differences and secular changes Tomohiro Ishii Received Received
  785-P3 Recurrent orchitis in a patient with true hermaphroditism Leticia Guimaraes de Souza SOUZA L. G. Received Received
  786-P3 Isolated persistent pubertal gynecomastia in three adolescent males as the only phenotypic expression of PAIS with androgen receptor gene mutations Pascal Philibert Received Received
  787-P3 Identical Twins Raised as Sister and Brother Rolf Peter Willig Received Received
  788-P3 Persistent Mllerian duct syndrome associated with anorchia caused by a compound heterozygous mutation in the AMHR-II gene Jaime Cruz-Rojo Received Received
  789-P3 A Novel Mutation in Steroidogenic Factor (SF1) Gene in a Patient with 46, XY DSD without Adrenal Insufficiency Ahmet ANIK Received Received
  790-P3 Evaluation of two new anti-Mllerian hormone (AMH) assays for the investigation of disorders of sexual development in neonates Clement Ho Received Received
  791-P3 Female, Male, or Between in a 46,XY-Patient with a 17-HSD3-Mutation Rolf Peter Willig Received Received
  792-P3 Physical assessment and growth curve of 46, XY Disorders of Sex Development children who aged 0-16 years old DI WU Received Received
  794-P3 A Novel Androgen Receptor Gene Mutation in a 46, XY Patient: Complete Androgen Insensitivity Syndrome Ece Bober Received Received
  795-P3 Polymorphisms and mutations of the genes INSL3 and HOXD13 in the pathogenesis of isolated cryptorchidism in Greece. SOFIA VAPPA Received Received
  797-P3 Screening for Y Microdeletions in Patients With Hypergonadotropic Hypogonadism Due to Disorder of Sexual Development murat karaoglan Received Received
  798-P3 I AM A BOY SINCE 8-YEARS-OLD:FEMALE DURING CHILDHOOD, VIRILIZATION AT PUBERTY Suna Kılınc Received Received
  799-P3 A novel mutation in human androgen receptor gene causing partial androgen insensitivity syndrome in a patient presenting with gynecomastia at puberty gonul catli Received Received
  800-P3 A novel mutation of the AMH in an Egyptian male with persistent Mullerian duct syndrome Mona El Gammal Received Received
  801-P3 PSEUDO-PRECOCIOUS PUBERTY IN ANDROGEN INSENSITIVITY SYNDROME SECONDARY TO A PREPUBERTAL ESTROGEN PRODUCING SERTOLI CELL TUMOR Dr Diana Monica Warman Received Received
  802-P3 Gender reassignment in Muslim communities Amir Babiker Received Received
  803-P3 A CASE OF KLINEFELTER SYNDROME WITH AN ATYPICAL PRESENTATION Nihal Hatipoglu Received Received
  805-P3 Patient with primary amenorrhea and glomerular nephropathy Franziska Phan-Hug Received Received
  806-P3 The advent of Disorders of sexual differentiation team at a major teaching Nigeria: impact on patient management and outcome. Olumide Jarrett Received Received
  808-P3 Characteristic of children with mixed gonadal dysgenesis Natallia Akulevich Received Received
  809-P3 A 19-year-old adolescent with short stature and scrotal tumor Katrin Heldt Received Received
  810-P3 An atypical case of Mayer-Rokitansky-Kuster-Hauser syndrome with hyperandrogenemia ALA STYOL Received Received
  811-P3 Cushings syndrome (CS) due to ectopic ACTH secretion by a germline tumor in the cross-tail area in a 7 month old female infant. Artur Bossowski Received Received
  812-P3 Uterine Bleeding: a rare side effect of mitotane treatment for recurrent adrenal carcinoma HILTON KUPERMAN Received Received
  813-P3 Metabolic syndrome in childhood acute lymphoblastic leukemia survivors Vincenza Luce Received Received
  814-P3 Results of growth hormone treatment in childhood brain tumors survivors Nadia Mazerkina Received Received
  815-P3 Craniopharyngioma symptoms, treatment and follow up an analysis of 100 cases Agnieszka Bogusz Received Received
  816-P3 Von Hippel-Lindau disease in an adolescent with a newly described alteration in the VHL gene Emine Aya Cimbek Received Received
  817-P3 TWO SYNCHRONOUS CENTRAL NERVOUS SYSTEM TUMOURS IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1. Rodica Elena Cornean Received Received
  818-P3 Endocrine evaluation in children and adolescents submitted to allogenic bone marrow tranplantation HILTON KUPERMAN Received Received
  819-P3 EARLY ENDOCRINE COMPLICATIONS IN SURVIVORS OF CHILDHOOD MALIGNANT TUMORS Cristina Sánchez-González Received Received
  820-P3 AIP POLYMORPHISM IN FAMILIAR ISOLATED PITUITARY ADENOMAS. CASE REPORT Verónica Figueroa Received Received
  821-P3 PRIMARY HYPOGONADISM AFTER HEMATOPOIETIC STEM CELL TRANSPLANT IN PEDIATRIC PATIENTS WITH CANCER maria del carmen de mingo alemany Received Received
  822-P3 Galactocele: A rare case of breast enlargement among children Moslah Ali Jabari Received Received
  823-P3 LHRH ANALOGUES (LHRHa) SUCCESSFULLY SUPPRESS MENSTRUATION DURING CHEMOTHERAPY IN TEENAGERS AND YOUNG ADULTS (TYA) Sujata Edate Received Received
  824-P3 Suprasellar brain tumours related endocrinopathies Amir Babiker Received Received
  825-P3 GROWTH HORMONE AND PROLACTIN SECRETING ADENOMA IN AN ADOLESCENT BOY Fatma Dursun Received Received
  826-P3 The evaluation of bone mass density (BMD) in patients after therapy of solid tumors Ewa Barg Received Received
  827-P3 The pathway to the true diagnosis Stoycheva Rositca Received Received
  828-P3 Long-term effects of a ketogenic versus a hypocaloric diet in children and adolescents with obesity. Ioanna Partsalaki Received Received
  829-P3 METABOLICALLY UNHEALTHY OBESE CHILDREN UNDER THE RISK OF EXERCISE INDUCED CHRONOTROPIC INCOMPETENCE Tetyana Chaychenko Received Received
  830-P3 Determinants of Serum Interleukin-1 Receptor Antagonist Concentrations in 12-Year-Old Children Born Small or Appropriate for Gestational Age Satu Sepp Received Received
  831-P3 Evaluation of Renal Functions in Obese Children and Adolescents with Cystatin-C and Creatinin Based GFR: Is Increasing GFR Reflected Hyperfiltration and Possible Renal Damage in Future? Zeynep SIKLAR Received Received
  832-P3 THE FRENCH EXPERIENCE IN BARIATRIC SURGERY Laparoscopic adjustable gastric banding (LAGB) IN ADOLESCENCE. Myriam DABBAS Received Received
  833-P3 Correlation of serum fibroblast growth factor 21 levels with metabolic parameters in Korean children and adolescents joonwoo Baek Received Received
  834-P3 Liver steatosis in obese children courses with enhanced insulin resistance and dyslipidemia, which are influenced by gender, puberty, race and body fat distribution. Gabriel Á. Martos-Moreno Received Received
  835-P3 HOW EARLY ARE VASCULAR CHANGES IN OBESE CHILDREN AMONG NORTH INDIAN POPULATION? Krishna Kishore Received Received
  836-P3 Prader-Willi Syndrome a general picture of 51 cases TIAGO JERONIMO DOS SANTOS Received Received
  837-P3 Comparison of two family-intervention (parents only versus parent and child) in the treatment of childhood obesity. Joseph Meyerovitch Received Received
  838-P3 Bioavailable Vitamin D in Obese Children: The Role of Insulin Resistance. Anna Grandone Received Received
  839-P3 AGE AT MENARCHE IN RELATION TO BODY MASS INDEX. DATA FROM THE HELLENIC ACTION PLAN FOR THE ASSESSMENT, PREVENTION AND TREATMENT FOR CHILDHOOD OBESITY ELLI ANAGNOSTOU Received Received
  840-P3 Are age and initial BMI-SDS in obese children and adolescents associated with the BMI-SDS courses during and after the attendance of an inpatient weight-loss program (LOGIC-trial)? Stephanie Brandt Received Received
  841-P3 Turn off and turn in: the influence of television viewing and sleep on lipid profiles in children. Melanie Henderson Received Received
  842-P3 Hepatic steatosis influences significantly the cardiovascular risk in children with metabolic syndrome Gianpaolo De Filippo Received Received
  844-P3 The risk of metabolic syndrome among dyslipidemic children and adolescents. Barbara Predieri Received Received
  845-P3 RNAi as tool to study molecular mechanisms of metabolic adverse reactions in Caenorhabditis elegans Manuela HORNLE Received Received
  846-P3 Hypertriglyceridemia in a boy with Bardet-Biedl Syndrome Case Report Ma&322;gorzata Wójcik Received Received
  847-P3 Uric acid and Triglycerides/HDL ratio as a predisposing factor for metabolic syndrome in children Andrea Paola Rojas Gil Received Received
  848-P3 Increased prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in GREECE Evangelia Charmandari Received Received
  849-P3 The triglyceride-to-high density lipoprotein cholesterol ratio in overweight Korean children YU SUN KANG Received Received
  850-P3 Waist Height Ratio As a Marker of Obesity and Insulin Resistance in Adolescents V. SRI NAGESH Received Received
  851-P3 Genotype and Clinical Characteristics in Korean patients with Prader-Willi Syndrome: a single center study Yoo-Mi Kim Received Received
  853-P3 Nonalcoholic steatohepatitis leading to cirrhosis of the liver as a complication of hypothalamic disorders in a course of craniopharyngioma- case report Urszula Watrobinska Received Received
  854-P3 Association of sleep habits and risk factors for metabolic disorders in children Andrea Paola Rojas Gil Received Received
  855-P3 Plasminogen activator inhibitor-1(PAI-1) as a marker of insulin resistance in obese adolescents Ozlem Engiz Received Received
  856-P3 Relationship between Visceral Obesity and Plasma Fibrinogen in Obese Children Noha Musa Received Received
  858-P3 Prevalence of asthma symptoms and association with obesity, sedentary lifestyle and sociodemographic factors: Data from the Hellenic National Plan for the Assessment, Prevention and Treatment of Childhood Obesity Feneli Karachaliou Received Received
  859-P3 Long-term effects of neonatal over-nutrition on metabolic equilibrium are age and sex dependant Pilar Argente Received Received
  860-P3 Metabolic syndrome in Greek adolescents and the effect of six-month educational/behavioral school interventions Flora Bacopoulou Received Received
  862-P3 Diagnosis and treatment of familial hypercholesterolemia in children a preliminary report. Agnieszka Brandt Received Received
  864-P3 A Systemic Approach for the Management of the Program entitled Development of a National System for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece Penio Kassari Received Received
  865-P3 Waist circumference to body height (WHtR) is a suitable measure of cardiovascular risk in overweight and obese children. Vira Yakovenko Received Received
  866-P3 The Effectiveness of a Comprehensive and Personalized Plan of Action in the Prevention and Management of Overweight and Obesity in Childhood and Adolescence Evangelia Charmandari Received Received
  867-P3 Insulin resistance in adolescents with screen addiction and attention-deficit/hyperactivity disorder Sukran Darcan Received Received
  868-P3 Ketogenic diet in paediatrics: work in progress Paola Miglioranzi Received Received
  869-P3 Severe hypothalamic obesity in a girl with craniopharyngioma case report. Monika Obara-Moszynska Received Received
  870-P3 The changes of neuroendocrine status in children with different forms of obesity Olga Zagrebaeva Received Received
  871-P3 Body composition and metabolic risk factors in preschool children. Mina Lateva Received Received
  872-P3 Assessment of impaired glucose tolerance and diabetes in an obese paediatric population Elowe-Gruau Eglantine Received Received
  873-P3 Sex differences in the pubertal response to high-fat diet Alejandra Freire Fernández-Regatillo Received Received
  874-P3 RELATION BETWEEN THYROID FUNCTION TESTS AND CARDIOMETABOLIC RISK FACTORS IN CHILDHOOD OBESITY Dogus Vuralli Received Received
  875-P3 Insulin infusion treatment option in severe hypertriglyceridemia induced pancreatitis ALA STYOL Received Received
  876-P3 Obesity has a significant impact on hyperandrogenemia only after puberty in Korean girls Min Jae Kang Received Received
  877-P3 Higher Hb1Ac in Obese Prader-Willi Syndrome patients versus Obese controls TIAGO JERONIMO DOS SANTOS Received Received
  878-P3 Obese children and adolescents: Reasons for non-compliance with follow-up scheduling Chrysoula Drosatou Received Received
  879-P3 Cardiometabolic risk factors in overweight/obese children and adolescents and family history of cardiovascular disease Zacharoula Karabouta Received Received
  880-P3 Healthcare professionals perception of overweight in preschool-aged children. Gianni Bocca Received Received
  881-P3 EVALUATION OF THE RELATIONSHIP BETWEEN SERUM ADROPIN LEVELS AND BLOOD PRESSURE IN OBESE CHILDREN AYA ALTINCIK Received Received
  882-P3 Adipocyte fatty acid binding protein (aFABP) is related to weight status and metabolic risk markers in childhood obesity Susann Blher Received Received
  883-P3 Investigating predisposing factors for childhood obesity Andrea Paola Rojas Gil Received Received
  884-P3 Vitamin D status in Iranian obese and non-obese children Fatemeh Sayarifard Received Received
  885-P3 IS VITAMIN D IMPORTANT PLAYER IN HEPATOSTEATOSIS IN CHILDHOOD OBESITY ? Elif Ozsu Received Received
  886-P3 Obesity in school children of Zahedan-Iran; double burden of weight disorders Fahimeh Soheilipour Received Received
  887-P3 Sports regulated and lipid profile in children and adolescents with overweight María Rosaura Leis Trabazo Received Received
  888-P3 Weight and the factors influencing it in a cohort of school aged children Pop Raluca-Monica Received Received
  889-P3 Dietary patterns in a group of obese children Pop Raluca-Monica Received Received
  890-P3 Does vitamin D influence energy metabolism in children and adolescents? Anna Wedrychowicz Received Received
  891-P3 Bone age assessment and glucose metabolism in overweight and obese children Corina Paul Received Received
  892-P3 The triglyceride-to-HDL cholesterol ratio is associated with insulin resistance in obese boys but not in obese girls Guy Massa Received Received
  893-P3 Experience with sleeve gastrectomy in adolescent obese subjects and in Prader-Willi Syndrome danilo FINTINI Received Received
  894-P3 Metabolic syndrome and inflammatory markers in obese childrenat Chiang Mai University Hospital Prapai Dejkhamron Received Received
  896-P3 Prevalence of excess weight in adolescents at primary health care units in South Brazil. Deisi Maria Vargas Received Received
  898-P3 A Case of rapid Onset Obesity, hypoventilation, hypothalamic dysregulation and neuroendocrine tumours-ROHHADNET syndrome Navoda Atapattu Received Received
  899-P3 The influence of physical activity and physical fitness in the metabolic profile and microcirculation of eutrophic, overweight and obese children 5 to 12 years of age Paulo Collett-Solberg Received Received
  900-P3 PREDICTING EARLY CARDIOVASCULAR RISK IN OBESE CHILDREN BASED ON ANTHROPOMETRY Giovanni Farello Received Received
  901-P3 Metabolic syndrome rates among adolescents of the Greek school community. Eleni Kotanidou Received Received
  902-P3 Identification and Management of Obesity by General Paediatricians in the UK. Madhu Easwariah Received Received
  903-P3 GENOTYPE AND PHENOTYPE CHARACTERIZATION IN TWO PATIENTS WITH MEHMO SYNDROME Juraj Stanik Received Received
  904-P3 Generalized idiopathic benign acanthosis nigricans in childhood Pinar Isguven Received Received
  905-P3 Potential connection of dyslipidemia with BMI and associated disorders in obese children and adolescents Lusine Navasardyan Received Received
  906-P3 Deficiency of 25- (OH) D-vitamin in adolescents with obesity. Mariia Matveeva Received Received
  908-P3 The prevalence of obesity in children and adolescents in the Udmurt Republic Tatiana Kovalenko Received Received
  909-P3 Survey Serum 25-Hdroxyvitamin D concentration in obese children and clinical significance in chinese population YU YANG Received Received
  910-P3 CLINICO-BIOCHEMICAL CORRELATION AMONG CHILDREN WITH OBESITY AND METABOLIC SYNDROME Sangeeta Yadav Received Received
  912-P3 IN DIFFERENT METHOD OF THE EVALUATIONOF STATE OF FEELING( cognitive functions/ socioemotional adaptation)OF OBESE CHILDREN;Goodenough Harris The Draw-A-Person Test AYA TREL ERGR Received Received
  913-P3 Phenotypic study of obesity in children and adolescents NORA SOUMEYA FEDALA Received Received
  914-P3 Association of serum levels of 25(OH)cholecalciferol and childhood obesity maria laura iezzi Received Received
  916-P3 Vitamin D deficiency can modulate GH/IGF-1 axis in growth hormone deficient children. Ewelina Witkowska-S&281;dek Received Received
  917-P3 Serum IGF-I concentration and growth during infancy correlate to polyunsaturated fatty acid pattern Jovanna Dahlgren Received Received
  918-P3 Are short children with low GH secretion metabolically different from children of normal height? Anders Tidblad Received Received
  919-P3 Familial short stature associated to terminal microdeletion of 15q26.3: variable phenotype not involving the IGF-I receptor gene. Laura Lucaccioni Received Received
  920-P3 Is the insulin secretion in pancreatic beta cells related with IGF-1/IGFBP-1 axis in Korean children? Min Sun Kim Received Received
  921-P3 SEVERE ISOLATED GROWTH HORMONE DEFICENCY AND MYOPATHY IN TWO BROTHERS WITH RNPC3 MUTATION Zoran Gucev Received Received
  922-P3 Gigantism Secondary to Growth Hormone Secreting Pituitary Macrodenoma ANDREW SNG Received Received
  923-P3 IGF-I and growth in early childhood in very-low-birth-weight infants and term appropriate for gestational age infants Miranda de Jong Received Received
  925-P3 Influence of The -202 A/C IGFBP-3 Promoter Polymorphism on Individual Variation in Body Height in Korean Girls Seung Yang Received Received
  927-P3 Comparison of two IGF-I assays in patients treated with GH María Martínez Barahona Received Received
  928-P3 Acute effects of a training session on IGF-I and IGFBP-3 concentrations in Brazilian Jiu-Jitsu fighters Carlos Martinelli Received Received
  929-P3 Biochemical profiles differentials by SGA children catch up Ignacio Diez Received Received
  930-P3 IGF-1 deficiency: an important differential diagnosis in severe growth failure and its excellent response to rhIGF-1 replacement therapy Dinesh Giri Received Received
  931-P3 Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency: our experience and review of the literature. Cristina Meazza Received Received
  932-P3 Modification of cardiovascular risk factors in children treated with growth hormone. MARIA ESCOLÀ LLOP Received Received
  933-P3 Adult height in children born small for gestational age and treated with GH: data from the French KIGS database HICHEM ZOUATER Received Received
  934-P3 Psychosocial functioning and self-perception of children and adolescents treated with Growth Hormone Chrysoula Drosatou Received Received
  935-P3 Do IGF-I Generation Test Results Predict First Year Growth Response to GH Treatment in Idiopathic Short Stature? Oya Ercan Received Received
  936-P3 Adherence to growth hormone treatment: impact of height, age, and puberty Thomas Reinehr Received Received
  937-P3 The Blood Oxidant System and Insulin Resistance in Girls with Turner Syndrome after 1 Year of Growth Hormone Therapy Maria Pankratova Received Received
  938-P3 An Open-label Phase 2 Dose-Finding Study Comparing 3 Different Doses of Weekly TV-1106 and Daily Recombinant Human Growth Hormone (Genotropin) in Treatment-Naive, Pre-Pubertal, Growth Hormone-Deficient Children Pippa Loupe Received Received
  939-P3 Increasing Lean Body Mass (LBM), Phase Angle (PA), and Total Body Water (TBW) but decreasing Body Fat (BF) among short-statured children born Small-for-Gestational Age on Growth Hormone Treatment Thomas Vlkl Received Received
  940-P3 Growth hormone (GH) dosing patterns in children with isolated GH deficiency (IGHD) and multiple pituitary hormone deficiency (MPHD) enrolled in the NordiNet International Outcome Study (IOS) Michael Maddalena Received Received
  941-P3 Decrease of small dense LDL and lipoprotein-associated phospholipase A2 due to human growth hormone treatment in short children with growth hormone deficiency and small for gestational age status Andreas Krebs Received Received
  942-P3 Long-term insulin sensitivity and beta-cell function in short children born SGA treated with GH and GnRHa: Results of a randomized, dose-response trial Manouk van der Steen Received Received
  943-P3 Influence of the application of the POI score on the results of GH therapy in Prader-Willi. Alessandro Salvatoni Received Received
  944-P3 The impact of growth hormone therapy in Noonan Syndrome children with identified mutations in RAS/MAPK pathway Alexsandra Malaquias Received Received
  945-P3 As great intra as interindividual variability in uptake of subcutaneous GH injections in longitudinally followed GH treated children Elena Lundberg Received Received
  946-P3 The correlation between the increase in insulin-like growth factor I and the growth improvement induced by growth hormone treatment in short children born small for gestational age Atsushi Hattori Received Received
  947-P3 Medical and biochemical effects of intervention program in patients with poor adherence to rhGH treatment. María Martínez Barahona Received Received
  948-P3 Favourable growth hormone treatment response in a young boy with achondroplasia Marina Krstevska-Konstantinova Received Received
  949-P3 Plexiform neurofibroma and demielinisant lesions in a patient with GH deficiency treated with rGH LUMINITA NICOLETA CIMA Received Received
  950-P3 Growth, development and puberty of patients with congenital multiple pituitary hormone deficiencies (MPHD) Zvi Laron Received Received
  952-P3 Linear regression model of final height prediction based on pre-treatment data in children with growth hormone (GH) deficiency treated with GH Maciej Hilczer Received Received
  953-P3 Vitamin D levels and not vitamin A are correlated with height velocity in children with growth hormone (GH) deficiency who are under GH treatment Maria Xatzipsalti Received Received
  954-P3 Long-term effects of GH replacement therapy on hematopoiesis in GH deficient children Andrea Esposito Received Received
  955-P3 Thyroid function in children treated with rhGH for growth hormone deficiency Athanasios Christoforidis Received Received
  956-P3 A 5-year follow-up of adults, with childhood-onset GH deficiency, treated with GENOTONORM in France hichem zouater Received Received
  957-P3 Somatotropic pituitary insufficiency in Kearns-Sayre syndrome the clinical picture, genetic diagnosis and efficacy of rhGH therapy Aleksandra Rojek Received Received
  958-P3 The correlation between the increase in insulin-like growth factor-I 24 hours after the first injection of growth hormone and the improved growth. Kenichi Miyako Received Received
  959-P3 Late diagnosis of a type II/III mucolipidoses treated with GH replacement therapy Iulia Crumpei Received Received
  960-P3 DOES APPLYING REGULAR QUESTIONNAIRE TO PATIENTS ON GROWTH HORMONE INCREASE THE COMPLIANCE ? Mikayir Genens Received Received
  961-P3 Characterization of Children Born Small for Gestational Age (SGA) Within the Australian Indications for Growth Hormone (GH) Therapy: An OZGROW Analysis Ian Hughes Received Received
  962-P3 Effectiveness of rhGH treatment in a boy with nephrogenic diabetes insipidus Clemens Kamrath Received Received
  963-P3 The Easypod Connect Observational Study (ECOS): comparison of results from interim analyses Ekaterina Koledova Received Received
  964-P3 EVALUATION OF THE FACILITY OF USE OF A NEW GROWTH HORMONE ADMINISTRATION DEVICE. STUDY DAGH2014. MARÍA JOSÉ RIVERO MARTÍN Received Received
  965-P3 Effect of human growth hormone on growth rate of short stature children with low birth weight Fatemeh Saffari Received Received
  966-P3 GH treatment and first year response: a retrospective study Catarina Moniz Received Received
  967-P3 Usefulness of reevaluation of Growth Hormone secretion during puberty Paolo Cavarzere Received Received
  969-P3 Evaluating First Year Response and Final Height to Growth Hormone Treatment in Growth Hormone Deficiency based on Peak GH levels on Testing SAYGIN ABALI Received Received
  970-P3 Growth hormone therapy in children: predictive factors and short-term and long-term response criteria in an Italian cohort Gabriella Pozzobon Received Received
  971-P3 PATIENTS WITH CHILDHOOD ONSET GROWTH HORMONE DEFICIENCY TREATED WITH rhGH REEVALUATION IN THE TRANSITION PERIOD BETWEEN CHILDHOOD AND ADULTHOOD PRELIMINARY STUDY Camelia Procopiuc Received Received
  972-P3 Time trends in age, growth hormone dose and height standard deviation score at treatment start Michael Maddalena Received Received
  973-P3 A patient with an 13q deletion syndrome, important growth delay and somatotropine insufficiency undergoing growth hormone therapy case report. Kinga Wolaniecka-Deahan Received Received
  974-P3 Linear Growth in a Child with Ellis Van Creveld Syndrome: Positive Effect of growth hormone therapy . Ashraf Soliman Received Received
  975-P3 Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome Serpil Bas Received Received
  976-P3 Thyroid function in children with Prader-Willi syndrome (PWS) treated with Growth Hormone (GH) Ian Hughes Received Received
  977-P3 Congenital hypopituitarism and severe developmental delay associated with homozygous POUF1 mutation. Maria Melikian Received Received
  978-P3 GH therapy in Lery Weill Syndrome: report of three cases Elisa Guidoni Received Received
  979-P3 The assessment of quality of life and new technologies for therapeutic monitoring in a cohort of pediatric patients treated with growth hormone Gabriella Pozzobon Received Received
  980-P3 Final height in patients with isolated growth hormone deficiency and multiple pituitary hormone deficiencies, treated with growth hormone Olga Berseneva Received Received
  981-P3 CURRENT PRACTICE IN DIAGNOSIS AND TREATMENT OF GROWTH HORMONE DEFICIENCY IN CHILDHOOD: A SURVEY FROM TURKEY SUKRAN POYRAZOGLU Received Received
  983-P3 Growth Hormone Therapy in Kuwait: Characteristics and Response in Treated Children Dalia Al-Abdulrazzaq Received Received
  984-P3 Management of prepubertal gynecomastia in two patients with Peutz-Jeghers Sydrome: use of aromatase inhibitors Laura Guazzarotti Received Received
  985-P3 Age at Menarche (AAM) in chronic respiratory disease: Cystic Fibrosis (FC) and Asthma. Comparison with a large cohort of healthy girls living in Verona. Claudia Piona Received Received
  986-P3 Optimal strategy for ovarian function assessment in girls with central precocious puberty before and during GnRH analogue treatment Maria Gabriela Ropelato Received Received
  987-P3 From prepuberty to adulthood: semen quality and its predictors in a prospective cohort study of Russian young men Oleg Sergeyev Received Received
  988-P3 Expanding the CHARGE geno-phenotype: a girl with novel CHD7 deletion, hypogonadotropic hypogonadism, and agenesis of uterus and ovaries Nele Reynaert Received Received
  989-P3 Metabolism and gonadal axis of early menarche girls and girls treated with GnRHa Chen Qiuli Received Received
  990-P3 The Consequences of Polycystic Ovary Syndrome in Adolescent Girls giorgiana brad Received Received
  991-P3 PELVIC MRI AS ALTERNATIVE TO PELVIC US FOR THE DIAGNOSIS OF PCOS IN OVERWEIGHT AND OBESE ADOLESCENT GIRLS. SIMON KAYEMBA-KAYS Received Received
  993-P3 The effect of aromatase inhibitor in a pubertal patient with aromatase excess syndrome Keisuke Nagasaki Received Received
  994-P3 Homozygous CYP17A1 mutation identified in a Chinese family with 46, XX and 46, XY 17a-hydroxylase deficiency Huamei Ma Received Received
  995-P3 Puberty and gonadal function in adolescent girls after renal transplantation. maud bidet Received Received
  996-P3 Endocrine disruptor and premature puberty, is there any association?. ISOLINA RIAÑO-GALAN Received Received
  998-P3 The Changes of Body Fat and Metabolic Parameters during GnRHa treatment in Central Precocious Puberty or Early and Fast Puberty Girls Chen Qiuli Received Received
  999-P3 SERTOLI CELL TUMOR IN A CASE OF ANDROGEN INSENSITIVITY SYNDROME senay savas erdeve Received Received
  1000-P3 Final height of children with SGA TREATED WITH BIOSYNTHETIC GROWTH HORMONE : About a serie of 30 children NORA SOUMEYA FEDALA Received Received
  1001-P3 Anti-Mllerian Hormone Is a Useful Marker of Gonadotoxicity in Girls Treated for Cancer: A Prospective Study Yoko Miyoshi Received Received
  1002-P3 Leydig-cell tumor, a rare cause of LH-independent sexual precocity in boys. maxime gerard Received Received
  1003-P3 Antimullerian Hormone and Inhibin B markers of the ovarian reserve after ovariectomy Morandi Grazia Received Received
  1006-P3 Early and sever manifestation of McCune-Albright syndrome with GNAS mutation in the liver tissue FAHAD ALJURAIBAH Received Received
  1007-P3 Depth And Timing Of Hypoglycaemia Achieved During Insulin Tolerance Test In Children Sze Choong Wong Received Received
  1008-P3 Presenting characteristics, auxological, and etiologic evaluation of 364 patients with growth hormone deficiency Huseyin Demirbilek Received Received
  1009-P3 Nutritional Supplementation, Sleep Patterns and Growth in Short and Lean Prepubertal Children Yael Lebenthal Received Received
  1010-P3 Disease-specific growth charts of Marfan syndrome in Korea SU JIN KIM Received Received
  1011-P3 Targeted birth length and parental height measurement in babies with birthweight 9th centile; improved uptake during second study during one calendar year in a single newborn unit. Colette Montgomery Sardar Received Received
  1012-P3 Case report of Wolf-Hirschhorn Syndrome by Chromosomal Microarray Analysis: Importance of the Molecular Investigation for the Etiological Diagnosis of Short Stature. RENATA MACHADO PINTO Received Received
  1013-P3 Achondroplasia height reference as a background matrix when following children with extreme short stature Andrea Merker Received Received
  1014-P3 Altered gene-expression in human growth plate cartilage tissue exposed to dexamethasone. Therése Cedervall Received Received
  1015-P3 Reversible Growth Hormone Excess (GHE) in Two Girls with Neurofibromatosis Type 1 (NF-1) and Optic Pathway Glioma (OPG) Ilaria Sani Received Received
  1016-P3 Autosomal recessive omodysplasia: a rare cause of disproportionate short stature CRISTIANE KOPACEK Received Received
  1017-P3 The growth characteristics of patients with Noonan syndrome, and first two years results of GH treatment: A Nationwide multicenter study ZEYNEP SIKLAR Received Received
  1018-P3 Vitamin D in short children on Growth Hormone Therapy: effects of vitamin D status and vitamin D supplementation on glucose homeostasis CRISTINA PATRICIA DUMITRESCU Received Received
  1021-P3 Response to rhGH treatment in patients with transient or permanent growth hormone deficiency Beatriz Villafuerte Q. Received Received
  1022-P3 Postnatal growth and biochemical markers of late preterm infants: prospective birth cohort Tomoko Yoshida Received Received
  1023-P3 ALTERATIONS OF SHOX AND ITS ENHANCERS AS A CAUSE OF SHORT STATURE: EVOLUTION OF OUR CASES MARIA LAURA BERTHOLT ZUBER Received Received
  1024-P3 Vitamin D Status in Pre-pubertal children with Isolated Idiopathic Growth Hormone Deficiency: Effect of Growth Hormone Therapy Rasha Hamza Received Received
  1025-P3 New point mutation in short stature homeobox (SHOX) gene leads to phenotype of Lery-Weill dyschondrosteosis. Gera Hoorweg-Nijman Received Received
  1026-P3 Fasting and post-meal levels of appetite regulating hormones, before and following growth hormone treatment, in children with idiopathic short stature Michal Yackobovitch-Gavan Received Received
  1027-P3 Impact of using WHO vs national growth charts on the clinical performance of a decision rule for growth monitoring Pauline SCHERDEL Received Received
  1028-P3 Comparison of the performance of algorithms proposed to standardize growth monitoring Pauline SCHERDEL Received Received
  1029-P3 Evaluation of 293 Danish Girls with Constitutional Tall Stature (CTS): Diagnostic Characteristics and Effects of Oral Administration of 17- Estradiol. Emmie Nicolina Upners Received Received
  1030-P3 Sitting height/height ratio: an indicator for genetic study of the SHOX gene in children with disharmonic short stature. An in-house analysis. Diego Yeste Received Received
  1031-P3 Final height in survivors of childhood acute leukemia In Ah Jung Received Received
  1032-P3 IMPACT OF RECOMBINANT HUMAN GROWTH HORMONE ON HEIGHT IN CHILDREN WITH CHRONIC KIDNEY DISEASE Polina Miteva Received Received
  1033-P3 Birth length and metabolic syndrome in obese children. elena inzaghi Received Received
  1034-P3 Birth characteristics influence the male to female diagnostic prevalence of idiopathic growth hormone deficiency Cecilia Camacho-Hbner Received Received
  1035-P3 Two cases with decelerated linear growth, normal growth hormone (GH) insulin-likegrowth factor I(IGF-I) axis with an exceptional response to GH therapy Fawziya Alyafei Received Received
  1036-P3 IMPACT OF GROWHT HORMONE (GH) TREATMENT IN CHILDREN FINAL HEIGHT AND WEIGHT STATUS Daniela Guelho Received Received
  1037-P3 Expanding the role of nurses in improving patient care and clinical outcomes in growth disorders Theo Bond Received Received
  1038-P3 Short stature in a rare 15q duplication is hGH treatment beneficial? Adina Manolachie Received Received
  1039-P3 Sotos syndrome. Why is an early diagnosis better? Maria Hawkins Received Received
  1040-P3 Psychomotor development in children born small for gestational age (SGA) during early infancy. Beatriz Puga Received Received
  1041-P3 PATIENT WITH CLASSIC PHENOTYPE OF HYPOCHONDROPLASIA AND DELETION OF THE GENE SHOX Sonia Amoretti Received Received
  1042-P3 Growth Hormone Treatment in Survivors of Pediatric Brain Tumors nurhan Ozcan Received Received
  1043-P3 Growth Hormone Deficiency in a patient with 4p16 Deletion: an infrequent association with Wolf-Hirschhorn syndrome Maria Xatzipsalti Received Received
  1044-P3 Value of alkaline phosphatase assay in short stature exploration NACCACHE Alexandre Received Received
  1045-P3 SGA incidence in one of the regions of the Russian Federation Irina Petrova Received Received
  1046-P3 Final Height (FH) in patients with and without pituitary abnormalities detected by MRI and/or CT treated with growth hormone. Maria Cláudia Schmitt-Lobe Received Received
  1048-P3 A Rare Cause of Short Stature : The Floating Harbor Syndrome.A Case Report. SIMON KAYEMBA-KAYS Received Received
  1049-P3 CORRELATIONS BETWEEN IGF1 LEVELS AND ANTHROPOMETRICAL PARAMETERS IN CHILDREN UNDER GROWTH HORMONE THERAPY SIMONA HUTU Received Received
  1050-P3 Body Mass Index is a Negative Predictor of Peak Stimulated Growth Hormone in Han Children with Short Stature Su Wu Received Received
  1051-P3 A 4 month-old boy with Beckwith Wiedemann Syndrome (BWS) Aleksandra Janchevska Received Received
  1052-P3 MEGHA : Observational study on prescription of the growth hormone Saizen in adults in France Laurente Fresneau Received Received
  1053-P3 Comparative study of low-dose growth hormone treatment in children with idiopathic short stature and growth hormone deficiency Hwalrim Jeong Received Received
  1054-P3 To investigate the changes of hormone levels and body composition in pubertal children with growth retardation: A clinical controlled study Su Wu Received Received
  1055-P3 the effect of BMI in reducing risk of refractory seizure due to probable lipoid tissue factors setila dalili Received Received
  1056-P3 Growth Hormone Treatment for Idiopathic Short Stature Renata Markosyan Received Received
  1057-P3 The frequency study and the Etiological profile of short stature in 2-15 years old children admitted in endocrinology clinic of 17 Shahrivar Hospital, Rasht, between 2008-2013 shahin koohmanaee Received Received
  1058-P3 Cystic encephalomalacia and infantile spasm as a complication of transient and mild hyperinsulinemic hypoglycemia Ahmet ANIK Received Received
  1059-P3 HYPERGLYCEMIA PRECEDED BY NEONATAL HYPERINSULINEMIC HYPOGLYCEMIA IN INFANTS WITH NOVEL HNF1A MUTATIONS Jana Malikova Received Received
  1060-P3 Transient congenital hyperinsulinism and renal Fanconi syndrome Corinna Melanie Brichta Received Received
  1061-P3 Clinical characteristics and molecular analysis of Turkish patients with congenital hyperinsulinism: A Single-Center Experience with 15 cases Sebahat Yilmaz Agladioglu Received Received
  1062-P3 Congenital Hyperinsulinemic Hypoglycemia of Infancy, Renal Fanconi Syndrome and Hepatopathy due to a Mutation in the HNF4A Gene Alejandro Vargas Pieck Received Received
  1063-P3 Genotype-phenotype associations in 90 children with congenital hyperinsulinism Maria Melikyan Received Received
  1065-P3 Glycogen-Storage Disease Type VI in a girl presenting with Recurrent Ketotic Hypoglycaemia but no Hepatomegaly Victoria Price Received Received
  1066-P3 Congenital hyperinsulinism in a newborn with a novel paternally inherited heterozygous mutation ( p.E1517G ) in the ABCC8 gene Nancy Elbarbary Received Received
  1067-P3 Discontinuation of Diazoxide therapy in children with Hyperinsulinaemic Hypoglycaemia with no identified genetic aetiology. A long-term follow-up study. Mouza Said AlYahyaei Received Received
  1068-P3 Pancreatic hormones in children with hyperinsulinaemic hypoglycaemia Maria Gemes Received Received
  1069-P3 Experience based on 193 18-F-DOPA PET CTs in patients with congenital hyperinsulinism: Pearls and pitfalls in imaging diagnostics in patients with CHI Oliver Blankenstein Received Received
  1070-P3 Severe neonatal hypoglycemia in the newborn despite prenatal diagnosed cerebral midline malformations A review of three cases Felix Reschke Received Received
  1071-P3 A case of mild congenital hyperinsulinemia presenting with developmental delay, complicated by diazoxide-induced transient neutropenia Yuki Abe Received Received
  1072-P3 Failure of Sirolimus response on three more cases with a diffuse type of Congenital hyperinsulinism Angham Al Mutair Received Received
  1073-P3 Auxological characteristics of persistent hyperinsulinemic hypoglycemia at birth Hironori Shibata Received Received
  1074-P3 Congenital hyperinsulinism in siblings case report. Agnieszka Brandt Received Received
  1075-P3 GENETIC CAUSES OF CONGENITAL HYPERINSULINISM IN SLOVAKIA Juraj Stanik Received Received
  1076-P3 Hyperinsulinism secondary to congenital portosystemic shunt in a neonate Yong Hee Hong Received Received
  1077-P3 Clinical presentation of a patient with a novel homozygous mutation in the TRPM6 gene. AYA ALTINCIK Received Received
  1078-P3 Long acting somatostatin analogs in the management of congenital hyperinsulinism in cases with poor compliance to conventional therapy Mehmet Nuri Ozbek Received Received
  1079-P3 Isolated Postprandial Hyperinsulinaemic Hypoglycaemia Maria Gemes Received Received
  1080-P3 Severe Congenital Hyperinsulinism in a Neonate Homozygous for Two Novel Missense Mutations in the KCNJ11 Gene Alev Ozon Received Received
  1081-P3 Congenital glucose-galactose malabsorption in a male infant Nevenka Slaveska Received Received
  1083-P3 Cholestatic hepatopathy and hypoglycaemic seizures as primary manifestation of hypocortisolism in infancy Peter Saupp Received Received
  1084-P3 Plasma Kisspeptin Levels of Infants Breast Growth in Neonatal Period Avni Kaya Received Received
  1085-P3 Circadian variation in cortisol concentration in mothers milk. Bibian van der Voorn Received Received
  1087-P3 Differences in leptin levels between newborns with and without Intrauterine Growth Restriction born in the Hospital Gineco Obstétrico Isidro Ayora of Quito-Ecuador. Year 2013-2014. Maria Elisa Acosta de la Vega Received Received
  1088-P3 Leptin and Neuropeptide Y Levels in Newborns Avni Kaya Received Received
  1089-P3 CORD BLOOD AND MATERNAL SERUM INSULIN-LIKE GROWTH FACTOR-I,II(IGF-I,II) , INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3 (IGFBP-3) LEVELS IN OVERWEIGHT PREGNANTS Aysehan Akinci Received Received
  1090-P3 Crystal formation in the meibomian glands as diagnostic proof of pseudohypoaldosteronism type I van der Werf-Grohmann Natascha Received Received
  1091-P3 TRANSIENT NEONATAL HYPOPARATHYROIDISM SECONDARY TO AN UNKNOWN MATERNAL PARATHYROID ADENOMA Maria Teresa Pérez Received Received
  1092-P3 Relations of birth chest circumference to blood serum Insulin-like Growth Factor-I in the newborn free of life-threatening disease: possible role of birth body weight in addition to respiratory supportive treatment. Cesare Terzi Received Received
  1093-P3 Relations of birth chest circumference to blood serum Insulin-like Growth Factor Binding Protein-3 in the newborn free of life-threatening disease: relevance of birth body weight and of blood serum Insulin-like Growth Factor-I beyond respiratory Cesare Terzi Received Received
  1094-P3 EPIPEG-PREMEB proyect. Clinical situation before 12 mouths go on a SGA population Ignacio Diez Received Received
  1095-P3 McCune-Allbright syndrome in a male newborn with hyperthiroydism María de la Esperanza Rueda Valencia Received Received
  1096-P3 Role of Notch1-Dll4 signaling pathway in mice model of oxygen-induced retinopathy Wangkai Liu Received Received
  1098-P3 Case Presentation; A Neonate Presenting to a District General Hospital with Isolated Cranial Diabetes Insipidus Evolving to Partial Hypopituitarism Gemma Keelty Received Received
  1099-P3 Isolated Growth Hormone Deficiency (IGHD) Associated with 7q11.23 Duplication Syndrome -a Case Report Ani Aroyo Received Received
  1100-P3 Cushing disease in a patient with Beckwith Wiedemann: an unusual association. FREDERIC BRIOUDE Received Received
  1101-P3 Baseline characteristics, growth hormone response, and long term evolution in 67 patients with pituitary stalk interruption according to the initial presentation Céline Bar Received Received
  1102-P3 Clinical characteristics of children with congenital combined growth hormone deficiency without associated syndrome in Belgium Renate Zeevaert Received Received
  1103-P3 Pitfalls in reporting of paediatric pituitary scans Dalia Hammouche Received Received
  1104-P3 Long term follow-up of a child treated with CyberKnife radiosurgery for ACTH-secreting pituitary adenoma after bilateral adrenalectomy Tommaso Aversa Received Received
  1105-P3 Off-label use of vaptans in children with severe symptomatic hyponatremia due to SIADH Gerdi Tuli Received Received
  1106-P3 Acquired long QT syndrome in a 14-year-old boy with panhypopituitarism Yoo-Mi Kim Received Received
  1107-P3 Between three to four years after severe traumatism brain injury 22 at least of children and adolescents do have persistent pituitary dysfunction Hélène Crosnier Received Received
  1108-P3 Causes and consequences of thickened pituitary stalk found by MRI in children and adolescents with central diabetes insipidus Martinez-Villanueva Julian Received Received
  1109-P3 Acute phase proteins and endocrine dysfunction after traumatic brain injury in childhood CHRISTINA KANAKA-GANTENBEIN Received Received
  1110-P3 Two Cases of Combined Pituitary Hormone Deficiency Proven to Have Mutations of GLI2 Yuka Nagashima Received Received
  1111-P3 AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus Doga Turkkahraman Received Received
  1112-P3 A boy with Combined Pituitary Hormone Deficiency and Agenesis of Right Internal Carotid Artery: a rare association or a simple coincidence? Carolina Ramos Received Received
  1113-P3 A rare case of Congenital Hyperinsulinism associated with Hypopituitarism due to Pituitary Stalk Interruption Syndrome Hussain Alsaffar Received Received
  1114-P3 Management of Risperidone induced Hyperprolactinemia in an Adolescent with Severe Autism Dinesh Giri Received Received
  1116-P3 HORMONE DISORDER AND VITAMIN DEFICIENCY IN ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) AND AUTISM SPECTRUM DISORDERS (ASD) Murat Dogan Received Received
  1117-P3 Two novel mutations in GLI2 gene in two unrelated Argentinean prepuberal patients, one with isolated growth hormone deficiency, and another with multiple pituitary hormone deficiency, both with developmental defects in posterior pituitary gland. Roxana Marino Received Received
  1118-P3 Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia Gonul Catli Received Received
  1119-P3 PEDIATRIC CENTRAL NERVOUS SYSTEM GERM CELL TUMORS: ENDOCRINE OUTCOME Alicia Torralbo-Carmona Received Received
  1120-P3 Description of patients diagnosed with central diabetes insipidus, 14 year experience at the National Childrens Hospital, Costa Rica. Fred Cavallo Received Received
  1121-P3 Pegvisomant in childhood acromegaly : report of two cases. Anna Vaczlavik Received Received
  1122-P3 Case Series; Central Diabetes Insipidus Presenting to a District General Hospital Gemma Keelty Received Received
  1123-P3 A 5-year-old patient with Cushings disease Kikumi Ushijima Received Received
  1124-P3 Sequelae in giant prolactinoma in a teenage boy. Sara Queirolo Received Received
  1125-P3 COMBINED PITUITARY HORMONE DEFICIENCY Karolina Kot Received Received
  1126-P3 Outstanding growth response to growth hormone replacement therapy in 3 different cases of growth hormone deficiency (GHD) Ljiljana Saranac Received Received
  1127-P3 Pituitary Stalk Interruption Syndrome : a case of an infant Havva Nur Peltek Kendirci Received Received
  1129-P3 Thickened Pituitary stalk with central diabetes insipidus: what diagnosis? merazka amel Received Received
  1130-P3 CLINICAL FEATURES AND PUBERTAL TIMING IN GIRLS WITH PREMATURE ADRENARCHE Heves Kirmizibekmez Received Received
  1131-P3 Growth Outcomes in Childhood Craniopharyngioma: A Longitudinal Assessment of 20 Cases at a Single Centre Maria Michaelidou Received Received
  1132-P3 Effects of GnRH agonists and antagonists on Danazol-induced precocious puberty rat Aram Yang Received Received
  1133-P3 Clinical Characteristics of Girls with Atypical Precocious Puberty Laura Mawer Received Received
  1134-P3 Paraphilic compulsion secondary to dopamine replacement therapy and successful treatment with gonadotropin-releasing hormone (GnRH) analogues Anna Brewka Received Received
  1135-P3 Cardiovascular disease risk factors in girls with isolated premature pubarche. Deisi Maria Vargas Received Received
  1136-P3 Menstruation Pattern in Idiopathic Central Precocious Puberty (ICPP) Girls after Discontinuing Gonadotropin-Releasing Hormone Agonist (GnRHa) Therapy Suttipong Wacharasindhu Received Received
  1137-P3 Age of menarche and near final height after long-term use of gonadotropin-releasing hormone agonist or combined with growth hormone in idiopathic central precocious girls Heon-Seok Han Received Received
  1138-P3 Psychosocial changes after GnRH agonist treatment in girls with idiopathic central precocious puberty Seung Yang Received Received
  1139-P3 Multicenter study of early screening and prevention of Prader-Willi Syndrome Wei LU Received Received
  1140-P3 A novel GLUT-1 mutation in a patient with apparently normal cerebrospinal fluid glucose level ALA STYOL Received Received
  1141-P3 Does treatment with gonadotropin releasing hormone (GnRH) analogues affect BMI in children with precocious or early puberty? Madhavi Madhusudhana Received Received
  1142-P3 Qualitative assessment of precocious puberty-related user-created contents on YouTube Hyo-Kyoung Nam Received Received
  1143-P3 Premature adrenarche is associated to precocious thelarche but not to precocious gonadarche or pubarche in Chilean adolescents Veronica Mericq Received Received
  1144-P3 Central precocious puberty in cerebral palsy. Patrizia Bruzzi Received Received
  1145-P3 Changes in body mass index during gonadotropin-releasing hormone agonist treatment in girls with idiopathic central precocious puberty and early pubety. Hae Sang Lee Received Received
  1146-P3 An Elevated Tumor Marker and Adrenarche in a Child using Lavender Oil - a case report Susan Lathrop Received Received
  1147-P3 Persistent isolated cyclical vaginal bleeding (premature menarche) not associated with GnRH pubertal response or endometrial echo should be considered for examination under general anaesthesia (EUA) Swathi Upadrasta Received Received
  1148-P3 Endocrine Dysfunction in Hypothalamic Hamartoma Depends on Presentation (endocrine or epileptogenic), Radiological Characteristics and Surgery Elisabetta Caredda Received Received
  1149-P3 Idiopathic central precocious puberty treatment criteria Joana Serra-Caetano Received Received
  1150-P3 Physiological dose reverse rhythm testosterone treatment abolishes the development of permanent gynaecomastia in adolescent boys with 47,XXY Klinefelter syndrome Gary Butler Received Received
  1151-P3 Urinary bisphenol A and its relation with kisspeptin in girls with idiopathic central puberty precocious and premature telarche lker Tolga Ozgen Received Received
  1152-P3 Prevalence of parental consanguinity in children with precocious puberty and kisspeptin gene polymorphisms Mahin Hashemipour Received Received
  1153-P3 EFFECTS OF NUTRITION AND VITAMIN D DEFICIENCY ON CENTRAL PUBERTY PRECOCIOUS Heves Kirmizibekmez Received Received
  1155-P3 Familial precocious puberty: clinical characteristics and GnRH agonist response Hwalrim Jeong Received Received
  1156-P3 Eating disorders in Greek adolescents: frequency and characteristics Eleni Kotanidou Received Received
  1158-P3 Evaluation of the effect of two different GnRH-agonist therapies on the anthropometric measurements in girls with idiopathic central precocious puberty (ICPP) AYLA GVEN Received Received
  1159-P3 Testotoxicosis: be careful to predict the final height Leticia Guimaraes de Souza SOUZA L. G. Received Received
  1160-P3 Central precocious puberty presented due to late started treatment for familial testotoxicosis Yilmaz Kor Received Received
  1162-P3 Delayed puberty in girl : clinical and etiologic study ALI EL MAHDI HADDAM Received Received
  1163-P3 Pubertal development anticipation Elisa Guidoni Received Received
  1164-P3 The Relationship between Xenoestrogens exposure and early puberty among young females living in Jeddah, Saudi Arabia. nouf alnwasany Received Received
  1165-P3 ONE YEAR FOLLOW-UP OF CHILDREN WITH ASYMPTOMATIC PRECOCIOUS PUBERTY: CLINICAL AND LABORATORY CHARACTERISTICS Cheol Woo Ko Received Received
  1168-P3 Endocrinopathies in a 17-years-old girl with Diamond-Blackfan anemia and transfusion-associated iron overload Elena Ilyina Received Received
  1169-P3 Large goiter in a patient with congenital hypothyroidism. Anna Bolmasova Received Received
  1170-P3 TOPICAL IODINE INDUCED THYROTOXICOSIS IN A NEWBORN WITH GIANT OMPHALOCELE Sonali Malhotra Received Received
  1171-P3 A familial case of congenital hypothyroidism (CH) due to a mutation in the thyroglobulin (TG) gene detected by Next Generation Sequencing (NGS) Maria Cristina Vigone Received Received
  1172-P3 Central hypothyroidism and growth hormone deficiency in a boy with Williams-Beuren Syndrome Sara Ciccone Received Received
  1173-P3 Avoidable thiamazole-induced omphalomesenteric duct remnants -20-year retrospective study in our hospital- Hiroyuki Shinohara Received Received
  1174-P3 The impact on families of receiving a diagnosis of congenital hypothyroidism Sabah Alvi Received Received
  1175-P3 Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: an observational study over 20 years Maurizio Delvecchio Received Received
  1176-P3 Graves disease in childhood and adolescence: clinical manifestations, adverse effects, and predictive factors for response to antithyroid drugs Noelia Vanesa Dujovne Received Received
  1177-P3 The correlation between TSH levels and BMI percentiles in hypothyroid children who are chemically euthyroid on levothyroxine treatment Carla Minutti Received Received
  1178-P3 Short Stature with lipodystrophy: reminder of a forgotten syndrome Rakesh Kumar Received Received
  1179-P3 Plasma visfatin level and its association with apolipoproteins A1 and B in hypothyroid children Elham Hashemi Dehkordi Received Received
  1180-P3 Outcome of thyrotoxicosis in childhood and adolescence in a geographically define area;a 24-year experience mariam kourime Received Received
  1181-P3 Early discrimination between transient and permanent congenital hypothyroidism in children with eutopic gland Maria Francesca Messina Received Received
  1182-P3 The role of early thyroid imaging in children with congenital hypothyroidism Tal Oron Received Received
  1183-P3 EFFECT OF MARIJUANA USE ON THYROID FUNCTION AND AUTO IMMUNITY Sonali Malhotra Received Received
  1184-P3 pediatric thyroid disease: About a series of 48 cases HAKIMA ABAES Received Received
  1185-P3 Neonatal hyperthyroidism with craniolacunia junko igaki Received Received
  1186-P3 Is transient hypothyroidism in preterm infants true? Beatriz Garcia Cuartero Received Received
  1187-P3 The benefits of preterm neonate development by early replacement therapy with L-thyroxine longitudinal prospective study Iwona Ben-Skowronek Received Received
  1188-P3 INTRATHYROIDAL ECTOPIC THYMIC TISSUE MIMICING A THYROID NODULE: A REPORT OF THREE PEDIATRIC CASES Gulay Karaguzel Received Received
  1189-P3 Simultaneous occurrence of thyroid storm, diabetic ketoacidosis, and multiple cerebral infarction in a 16-year-old girl Sung Yeon Ahn Received Received
  1190-P3 Two Cousins with Allen-Herndon-Dudley Syndrome: A Novel Mutation on MCT8 Gene Gul Yesiltepe Mutlu Received Received
  1191-P3 Audit of Thyroid Carcinoma in children, adolescents and adults Wei Li Cindy HO Received Received
  1193-P3 NKX2-1 p.Asp266Argfs142X de novo mutation in a girl with congenital hypothyroidism (CH): phenotypic description Boris Stoilov Received Received
  1194-P3 Development and risk factors of thyroid dysfunction in patients with positive TPO antibodies Nicolas Gomez Carmen Received Received
  1195-P3 The evaluation of CD8CD122 T cells in children with autoimmune thyroiditis. Anna Kucharska Received Received
  1196-P3 Hoffmann syndrome in a boy with severe acquired primary hypothyroidism. Lucía Garzón Received Received
  1197-P3 Congenital Hypothyroidism incidence and dysgenesis or dyshormonogenesis prevalence in a large infants cohort from south of France. Isabelle OLIVER PETIT Received Received
  1198-P3 Thyroid function in a large group of obese children: causes and consequences Fiorenzo Lupi Received Received
  1199-P3 THYROID NODULES IN CHILDREN AND ADOLESCENTS Concepción Fernández Ramos Received Received
  1200-P3 Trisomy 21 and thyroid dysfunction: About 50 pediatric cases ALI EL MAHDI HADDAM Received Received
  1201-P3 NKX2-1 (TTF-1) Germline mutations are not a frequent cause of congenital hypothyroidism due to dysgenesis AIDY GONZALEZ Received Received
  1202-P3 A Curious Case of Thyrotoxic Crisis and Lower Extremity Weakness in a 15 year-old Female with Graves Disease Magdalena Dumin Received Received
  1203-P3 Newborns of Mothers with GravesDisease survey of 14 years Rita Cardoso Received Received
  1204-P3 Use of liothyronine in a case of consumptive hypothyroidism caused by hepatic hemangiomas Shinji Higuchi Received Received
  1205-P3 Subclinical hypothyroidism in children and adolescents a 5-year single-center follow-up study Aleksandra Antosz Received Received
  1206-P3 The difference between cord and filter paper TSH level in congenital hypothyroidism screening programme FAHAD ALJURAIBAH Received Received
  1207-P3 Neonatal hyperthyrotropinemia - watchful waiting versus treatmentExperiences from a tertiary centre caroline ponmani Received Received
  1208-P3 Congenital central hypothyroidism due to a homozygous mutation in the TSHB gene just think about it Monika Flury Received Received
  1209-P3 A Case of Acute Suppurative Thyroiditis with Piriform Sinus Fistula treated with Chemocauterization using Trichloroacetic acid Kyung lae Son Received Received
  1210-P3 Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated? Elena Sukarova-Angelovska Received Received
  1211-P3 Rectal diluted levothyroxine for the treatment of neonatal hypothyroidism: an alternative route of administration Marina Ybarra Received Received
  1213-P3 HYPERTHYROIDISM IN CHILDREN AND ADOLESCENTS:CAUSES, WHEN AND HOW TO TREAT. A TUNISIAN EXPERIENCE ESSADDAM Leila Received Received
  1214-P3 Massive pericardial effusion and short stature caused by autoimmune hypothyroidism in 9-yr old dyspneic girl Heon-Seok Han Received Received
  1215-P3 Prevalence of goiter and thyroid nodule and analysis of the association between anthropometric measurements and thyroid volume in children Murat Dogan Received Received
  1216-P3 Hyperfunctioning Thyroid Nodule in an Adolescent Inka Baus Received Received
  1217-P3 Subclinical hypothyroidism in children and adolescents : About a study of 25 cases NORA SOUMEYA FEDALA Received Received
  1218-P3 Impaired Hemorheological Parameters and Increased Carotid Intima-Media Thickness in Children with Subclinical Hypothyroidism Sebahat Yilmaz Agladioglu Received Received
  1219-P3 Unilateral Graves Disease in an adolescent: Case report Beray Selver Eklioglu Received Received
  1220-P3 Transient Hyperthyroidism Associated with a Thyroid Nodule Alejandro Vargas Pieck Received Received
  1221-P3 Hyalinizing Trabecular Tumor of thyroid gland in 17-year-old boy- case report Beata Sawiclka Received Received
  1222-P3 SEVEN CASES WITH WILLIAMS BEUREN SYNDROME: ENDOCRINE EVALUATION AND LONG TERM FOLLOW-UP Ayla Gven Received Received
  1223-P3 Clinical course in a girl with hTPO mutation R161I in exon 5: 18 years of follow up Boris Stoilov Received Received
  1224-P3 Transient polyarthritis with Carbimazole treatment Madhavi Madhusudhana Received Received
  1226-P3 A rare adverse effect of radioactive iodine therapy in a child with Graves Disease Elizabeth Walsh Received Received
  1227-P3 A 7 month-old male infant with spontaneous transient Graves thyrotoxicosis Shuichi Yatsuga Received Received
  1228-P3 Sex and age differences in the incidence of thyroid disease in children with obesity Olena Budreiko Received Received
  1229-P3 Euthyroid sick syndrome in children presenting with diabetic ketoacidosis Huseyin Demirbilek Received Received
  1230-P3 THE ROLE OF THYROID FINE-NEEDLE ASPIRATION CYTOLOGY IN THE TREATMENT AND FOLLOW-UP OF THYROID NODULES IN THE PEDIATRIC POPULATION mikayir genens Received Received
  1231-P3 ANGIONEUROTIC EDEMA WITH ANTITHYROID DRUGS IN THYROID STORM: WHAT IS THE BEST THERAPEUTIC OPTION Pelin Bilir Received Received
  1232-P3 Malabsorption of levothyroxine in a child affected by short bowel syndrome Laura Paone Received Received
  1233-P3 Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group Ediz Yesilkaya Received Received
  1234-P3 Cardiovascular Assessment In Turner Syndrome: Current Practice In The United Kingdom Avril Mason Received Received
  1235-P3 Turner syndrome in Iceland 1968-2012. Congenital anomalies and clinical outcomes. Arndis Sigmarsdottir Received Received
  1237-P3 Clinical Features and Genetic Considerations of Turner Syndrome: A Review of our cases Sara Berrade Received Received
  1238-P3 Growth characteristics of patient with Turner syndrome different age and karyotypes by the Ukrainian national register. Natalia Zelinska Received Received
  1239-P3 Nationwide study of Turner syndrome in Ukraine. Irina Shevchenko Received Received
  1240-P3 Patients with Turners syndrome should have ophthalmological examination before commencing recombinant growth hormone treatment Hussain Alsaffar Received Received
  1241-P3 Renal problems in early adult patients with Turner syndrome WOO YEONG CHUNG Received Received
  1242-P3 To predict ovarian function is a single determination of AMH usefulin patients with Turner syndrome? Paolo Cavarzere Received Received
  1243-P3 Anthropometric findings from birth to adulthood in Turkish Girls with Turner Syndrome and association with Karyotpye distribution Ediz Yesilkaya Received Received
  1244-P3 GROWS HORMONE THERAPY IN TURNER SYNDROME Corina Galesanu Received Received
  1245-P3 A Rare Variant of Turner Syndrome: First Clinical Report from Kuwait mohamed kholoud Received Received
  1246-P3 Turner Syndrome with Breast Development : Case report Sung Won Park Received Received
  1247-P3 The association between ed endocrinopathies and central arterial pressure in children and adolescents Hanna Borysewicz-Sanczyk Received Received
  1248-P3 The Development of a Publication Presentation Workshop: Enhancing the Publication of African Paediatric Endocrinological Research. Francois de Villiers Received Received
  1249-P3 Leukocyte telomere length in young adults born preterm: support for accelerated biological ageing Carolina Smeets Received Received
  1250-P3 A survival analysis approach to assess the association between maternal prepregnancy overweight and childhood overweight Results of the Ulm Birth Cohort Study (UBCS) Stephanie Brandt Received Received
  1251-P3 Sexually dimorphic methylation of SF-1 gene in rat placenta after gestational exposure to BPA Julie Fudvoye Received Received
  1253-P3 Newborns with Longest Telomeres are Big at Birth and have Most Lean Mass not Most Fat in Late Infancy. Marta Díaz Received Received
  1254-P3 Untargeted Plasma Metabolomics in Prepubertal ICSI and naturally conceived Children Unravels Gender - dimorphic Metabolic Trajectories after ICSI Alexandra Gkourogianni Received Received
  1255-P3 Analysis of gene methylation difference and evaluation the effect of growth hormone in Silver Russell syndrome DI WU Received Received
  1256-LBP Higher Expression of the Oncogene YAP1, a Wnt/-Catenin Target, is associated with Poor Outcome in Pediatric Patients with Adrenocortical Tumors Sonir Antonini Received Received
  1258-LBP A Distinct Population of Islet Cells Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease Mark Dunne Received Received
  1259-LBP Adrenal Steroid Precursors Accumulating in Congenital Adrenal Hyperplasia lead to Transactivation of the Glucocorticoid Receptor Karijn Pijnenburg-Kleizen Received Received
  1261-LBP POLR3H VARIANT IS ASSOCIATED WITH PRIMARY OVARIAN FAILURE IN TWO FAMILIES Franca Monica Received Received
  1262-LBP The Existence Of An Androgen Responsive Transcriptome In The Peripheral Blood Of Boys Extends The Utility Of The HCG Stimulation Test Martina Rodie Received Received
  1266-LBP Determining the effects of race, skin colour and genotype on the response to vitamin D therapy. Jaya Sujatha Gopal-Kothandapani Received Received
  1267-LBP Safety and Efficacy of Long-Acting Growth Hormone (VRS-317) in Children with GHD: Effects of Dose Change in the Second Treatment Year Ingrid Koo Received Received
  1268-LBP GENETIC CAUSES OF DISPROPORTIONAL SHORT STATURE IDENTIFIED BY WHOLE EXOME SEQUENCING Mariana Funari Received Received
  1269-LBP Reduced Humanin Levels In Children With Type-1 Diabetes Mellitus Maria Isabel Hernandez Received Received
  1270-LBP Long-term Safety and Effectiveness of daily and weekly growth hormone treatment in pediatric patients Jae Hyun Kim Received Received
  1271-LBP Prepubertal and pubertal predictors of semen quality in a prospective cohort study of Russian young men: focus on endocrine disrupting chemicals Oleg Sergeyev Received Received
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EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

54th Annual ESPE Meeting 2015

 

1 - 3 October 2015 Barcelona, Spain
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                   DOI: 10.3252/pso.eu.54espe.2015 
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