EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

55th Annual ESPE Meeting 2016

 

10-12 September 2016 Paris
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Poster title
Applicant name
Status
  1-5-RFC A novel animal model to study 21-hydroxylase deficiency in vivo Andreas Zaucker Received Received
  1-7-RFC Recovery of adrenal function in children with asthma assessed by Low Dose Short Synacthen Test (LDSST) Arundoss Gangadharan Received Received
  1-4-RFC Mutations of ABCD1 in 16 Vietnamese Patients with X-linked Adrenoleukodystrophy Dung Vu Chi Received Received
  1-P1 Leptin is associated with serum aldosterone in paediatric subjects, independently of body mass index, blood pressure and plasma renin activity. Alejandro Martinez-Aguayo Received Received
  1-LBP 46,XY DSD due to isolated AMH deficiency resulting in Persistent Mllerian Duct Syndrome (PMDS) as a consequence of a single-base deletion in a SF1-response element of the AMH promoter Rodolfo Rey Received Received
  1-6-RFC Pediatric patients with congenital adrenal hyperplasia have unfavorable changes in their cardiovascular risk profile Christiaan Mooij Received Received
  1-2-RFC Glucocorticoid deficiency due to disruption of mitochondrial steroidogenesis leads to dysregulation of antioxidant pathways and nucleotide biosynthesis Meltem Weger Received Received
  1-8-RFC Adrenal dysfunction in HIV-exposed uninfected infants receiving ritonavir-boosted lopinavir, an HIV protease inhibitor, for the prevention of breastfeeding HIV transmission. An ANRS 12174 substudy. Michel Polak Received Received
  1-1-RFC Tracing the Glucocorticoid Receptor evolutionary pedigree: insights from a comprehensive phylogenetic analysis of the full NR super-family Penio Kassari Received Received
  1-3-RFC Impaired cardiac function in a mouse model of Generalized Glucocorticoid Resistance Penio Kassari Received Received
  2-4-RFC Results of orthopaedic surgery in children with X-linked hypophosphatemic rickets (XLHR) AGNES LINGLART Received Received
  2-1-RFC 25-OH-Vitamin D status in a pediatric population of subjects affected by Prader-Willi Syndrome compared to matched controls danilo FINTINI Received Received
  2-LBP Sexual Outcomes in Brazilian Patients with 46,XY DSD Patients Rafael Loch Batista Received Received
  2-2-RFC Sex-specific association between cord 25hydroxyvitamin D and sub-ischial leg length. An Odense Child Cohort Study. Anna Mathilde Egelund Christensen Received Received
  2-3-RFC Cord vitamin D is inversely associated with blood pressure in young girls, but not in boys. An Odense Child Cohort Study Ss Dragsbk Larsen Received Received
  2-8-RFC Final heights and BMI in patients affected with different types of pseudohypoparathyroidism hanna hanna Received Received
  2-P1 Mast cells and steroidogenesis in the human fetal adrenal Alexandre Naccache Received Received
  2-5-RFC Growth Patterns And Fractures In Boys With Duchenne Muscular Dystrophy:Insights From Over 800 Boys In The UK North Star Cohort Shuko Joseph Received Received
  2-7-RFC Effect of paternal loss-of-function mutations of GNAS on growth during the childhood: a role for XL. Lea Tran Received Received
  3-4-RFC Children and adolescents with severe TBI can develop late pituitary dysfunction independently of the results of the first pituitary evaluation. Yamina DASSA Received Received
  3-3-RFC Unraveling the Link Between Optic Nerve Hypoplasia and Pituitary Hormone Dysfunction Naseem Alyahyawi Received Received
  3-7-RFC Pituitary structural abnormalities in idiopathic isolated growth hormone deficiency Luis Cardoso Received Received
  3-6-RFC Priority target conditions of growth-monitoring in children: toward consensus Pauline SCHERDEL Received Received
  3-2-RFC Subfertility After Chemotherapy in PNET tumours: 34 Year Experience From a Single Centre (1980-2013) Joana Serra-Caetano Received Received
  3-1-RFC Endocrinopathy in Childhood Intracranial Germ Cell Tumours is Predicted by Disease Location not Treatment: 30 Year Experience From a Single Tertiary Centre Joana Serra-Caetano Received Received
  3-LBP The growth hormone (GH) - insulin like growth factor I (IGF-1) system in early non-alcoholic fatty liver disease: from an animal model to a childrens cohort. Tommaso de Giorgis Received Received
  3-8-RFC Anthropometric and endocrine features in children and adolescents with Type 1 Narcolepsy. Antonio Balsamo Received Received
  3-P1 Gender-specific differences in hypothalamus-pituitary-adrenal axis activity in children.A meta-analysis Bibian van der Voorn Received Received
  3-5-RFC PROSPECTIVE DYNAMIC EVALUATION OF HYPOTHALAMO-PITUITARY FUNCTION IN 30 CASES OF PAEDIATRIC CRANIOPHARYNGIOMA, BY HYPOTHALAMIC INJURY AND TREATMENT; A SINGLE CENTRE SERIES. Chiara Guzzetti Received Received
  4-8-RFC Novel association between the non-synonymous A803G polymorphism of the N-acetyltransferase 2 gene and impaired glucose homeostasis in obese children and adolescents. Giuseppina Rosaria Umano Received Received
  4-3-RFC Early growth is associated with fat accumulation and distribution measured by DXA in 982 healthy children aged 8 to 15 years Jeanette Tinggaard Received Received
  4-5-RFC Steroid Metabolomic Signature of Liver Disease in Childhood Obesity Aneta Gawlik Received Received
  4-LBP Sirolimus precipitating Diabetes in a patient with Congenital Hyperinsulinism due to autosomal dominant ABCC8 mutation ANTONIA DASTAMANI Received Received
  4-6-RFC Adipose tissue - a source of hyperandrogenism in obese females? Isabel Wagner Received Received
  4-2-RFC Adipocytokines delay pubertal maturation of human Sertoli cells Isabel Wagner Received Received
  4-1-RFC Immune-fat-bone axis in obese children: the role of LIGHT Brunetti Giacomina Received Received
  4-P1 Prepubertal children born large for gestational age have lower serum DHEAS concentrations than those with lower birth weight Henrikki Nordman Received Received
  4-7-RFC Prevalence and characterization of retinal alterations in a cohort of overweight and obese children Stefania Pedicelli Received Received
  5-P1 Whole exome sequencing in patients with Primary Generalized Glucocorticoid Resistance, who did not have mutations in the NR3C1 gene AMALIA SERTEDAKI Received Received
  5-2-RFC Limits of agreement between HbA1c levels measured in different laboratories following the introduction of the International Federation of Clinical Chemistry and Laboratory Medicine standardised values Joanne Blair Received Received
  5-6-RFC Clinical management of the Mitchell-Riley syndrome due to RFX6 gene mutations: aggressive support results in improved outcome Poidvin Amélie Received Received
  5-7-RFC Early successful hematopoietic cell transplantation (HSCT) in a boy with IPEX syndrome caused by novel c.721TC FOXP3 mutation Barbora Obermannova Received Received
  5-4-RFC TRANSIENT NEONATAL DIABETES IN ADULTHOOD: METABOLIC OUTCOMES kanetee busiah Received Received
  5-1-RFC Adiponectin and leptin in children with type 1 diabetes for 3-5 years with or without residual cell function. Niels Birkebaek Received Received
  5-5-RFC The efficacy of insulin degludec in children and adolescents with type 1 diabetes. Barbara Predieri Received Received
  5-3-RFC Sexual lifestyle among young adults with type 1 diabetes Orit Pinhas-Hamiel Received Received
  6-5-RFC Abnormal Videofluoroscopic Swallow Studies (VFSS) in Infants with Prader-Willi Syndrome Indicate a High Rate of Silent Aspiration Parisa Salehi Received Received
  6-3-RFC Effect of Very Early Growth Hormone (GH) Treatment on Long-term Growth in Girls with Turner Syndrome (TS): A Multicenter, Open-Label, Extension Study Hiren Patel Received Received
  6-2-RFC RAB3IP and DGCR8 as a potentially pathogenic novel candidate gene involving in growth disorders Thais Homma Received Received
  6-P1 Novel CYP11A1 mutations in 15 patients (13 families) with variable clinical presentations Claire Goursaud Received Received
  6-LBP Children with brain tumors have enhanced visceral adiposity compared to non-cancer controls: A preliminary analysis from the Canadian Study of Determinants of Endometabolic Health in Children (CanDECIDE) study M. Constantine Samaan Received Received
  6-4-RFC Growth hormone (GH) treatment in skeletal dysplasias Short-term results in prepubertal children reported in KIGS Ferah Aydin Received Received
  6-7-RFC Characteristics of responders and poor-responders to Increlex therapy data from children enrolled in the European Increlex Growth Forum Database (EU-IGFD) Nick Brown Received Received
  6-8-RFC The actual incidence of Small for Gestational Age (SGA) newborns and their catch-up growth is dramatically lower than previously considered. Eran Lavi Received Received
  6-6-RFC Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene Mutation Maria Consolata Miletta Received Received
  7-2-RFC Reference values for external genitalia size and steroid hormone levels in female neonates. Sarah Castets Received Received
  7-4-RFC A Mutation in WT1 (Wilms tumor suppressor 1) associated with 46,XX TDSD Caroline Eozenou Received Received
  7-LBP Loss of functional Osteoprotegerin: more than a skeletal Problem Corinna Grasemann Received Received
  7-1-RFC Tissue engineered collagen based tubular scaffolds for urethral regeneration. A novel technology for the surgical treatment of VSD (Variation of Sex Development) patients with severe hypospadias. Kalitha Pinnagoda Received Received
  7-3-RFC Harmonisation of Serum Dihydrotestosterone Analysis: Establishment of an External Quality Assurance Program Michaela Hartmann Received Received
  7-P1 Transient Generalized Glucocorticoid Hypersensitivity Syndrome Eleni Magdalini Kyritsi Received Received
  7-5-RFC FERTILITY PRESERVATION IN AN ADOLESCENT BOY: INDUCING PUBERTY AND SPERMATOGENESIS PRIOR TO BONE MARROW TRANSPLANTATION margaret zacharin Received Received
  7-6-RFC FERTILITY PRESERVATION FOR CHILDREN AND ADOLESCENTS A REPORT OF CURRENT PRACTICE Cindy Ho Received Received
  7-7-RFC Clinical Decision-Making in Disorders of Sex Development (DSD): Physician Recommendations Pre- and Post-Consensus Statement David Sandberg Received Received
  7-8-RFC Premature adrenarche in girls at pubertal onset is associated with high androgens, but lower AMH concentrations veronica mericq Received Received
  8-LBP Impact of weight loss after bariatric surgery on gonadic function in severely obese female adolescents Iva Gueorguieva Received Received
  8-8-RFC Efficacy of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-Month Complete Database Results of a Phase 2 Study in Children with Growth Hormone Deficiency Gili Hart Received Received
  8-7-RFC Safety and Tolerability of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-month Complete Dataset Results of a Phase 2 Study in Children with Growth Hormone Deficiency Gili Hart Received Received
  8-5-RFC Optimal Sampling of IGF-1 During Weekly Administration of a Long Acting Human Growth Hormone (MOD 4023) Gili Hart Received Received
  8-3-RFC Batch-to-Batch Consistency of a Highly O-Glycosylated Long-Acting Human Growth Hormone (MOD-4023) Gili Hart Received Received
  8-1-RFC Somavaratan (VRS-317) Treatment of Children with Growth Hormone Deficiency (GHD): Results at 2 Years (NCT02068521) Ingrid Koo Received Received
  8-2-RFC Pharmacokinetic Modelling predicts native hGH levels following administration of a sustained-release prodrug, TransCon hGH, to children with GHD. Michael Beckert Received Received
  8-6-RFC A Six-Month Safety and Efficacy Study of TransCon hGH Compared to Daily hGH in Pre-Pubertal Children with Growth Hormone Deficiency (GHD) Yi Su Received Received
  8-P1 The Effect of Obesity on the Stress Response: The Paradigm of Surgical Stress Voutetakis Antonis Received Received
  8-4-RFC A hybrid Fc-fused human growth hormone, GX-H9, shows a potential for weekly and semi-monthly administration in clinical studies Joan Lee Received Received
  9-1-RFC Neonatal diabetes due to NKX2.2 mutation Genotype, clinical phenotype and therapeutic challenges in a very low birth weight diabetic neonate Adi Auerbach Received Received
  9-3-RFC Molecular analysis of a large cohort of MODY patients by Next Generation Sequencing. Stefano Stagi Received Received
  9-4-RFC Prevalence of monogenic diabetes in the Lithuanian pediatric and young adult population Valerie Schwitzgebel Received Received
  9-5-RFC NON-MODY MONOGENIC DIABETES: A VERY HETEROGENOUS AND PROBLEMATIC GROUP OF DIABETES Zeynep SIKLAR Received Received
  9-P1 Long-term anthropometric outcome of girls with non-classical congenital adrenal hyperplasia diagnosed in childhood Rachel Bello Received Received
  9-2-RFC Missense mutation of GLIS3 gene resulting inneonatal diabetes and congenital hypothyroidism nadia alghazir Received Received
  9-LBP Osteoprotegerin and insulin resistance in childhood obesity: a new interplay? Eleni P Kotanidou Received Received
  9-6-RFC Emerging pitfalls of etiological diagnosis of diabetes in children and adolescents? Analysis of a French cohort of 310 recent-onset cases Elise Bismuth Received Received
  9-7-RFC Chronotype and Type 2 Diabetes Risk in Preadolescents Magdalena Dumin Received Received
  10-8-RFC GESTATIONAL DIABETES IS ASSOCIATED WITH CHANGES IN PLACENTAL MICROBIOTA AND MICROBIOME Judit Bassols Received Received
  10-2-RFC DYSREGULATION OF PLACENTAL MIRNA IN MATERNAL OBESITY IS ASSOCIATED WITH PRE-AND POST-NATAL GROWTH Judit Bassols Received Received
  10-3-RFC Vitamin D depletion in pregnancy decreases survival time, oxygen saturation, lung weight and body weight in preterm rat offspring. Sine Lykkedegn Received Received
  10-4-RFC Pharmacokinetics of Intravenous Glucagon in Children with Hyperinsulinaemic Hypoglycaemia PRATIK SHAH Received Received
  10-5-RFC Phenotype, Genotype and Short term Outcome in Congenital Hyperinsulinism(CHI) MUDITA DHINGRA Received Received
  10-LBP Molecular analysis of AR, SRD5A2, NR5A1 and HSD17B3 genes in a Brazilian 46,XY DSD cohort. Reginaldo Petroli Received Received
  10-P1 Current Dilution Methods cause Large Variations and Inaccuracies when making up 1mcg Synacthen Dose. Alexandra Cross Received Received
  10-6-RFC Increased Islet Cell Neogenesis and Endocrine Cell Differentiation in Congenital Hyperinsulinism in Infancy Mark Dunne Received Received
  10-1-RFC Paternal loss-of-function mutations of GNAS and growth retardation in a mice model: a specific placental transcriptomic signature? Lea Tran Received Received
  11-6-RFC Falsely TSH and free thyroid hormone measurements in pediatric patients treated with high dose of biotin Moran Gal Received Received
  11-3-RFC Germline and somatic DICER1 mutations in familial Papillary Thyroid Carcinoma and Multinodular Goiter. César Lumbreras Received Received
  11-LBP Long-term Safety and Effectiveness of Growth Hormone Treatment in Pediatric Patients with Growth Hormone Deficiency : Interim Results of LG Growth Study Sochung Chung Received Received
  11-1-RFC Central hypothyroidism and biallelic defect near the D/ERY motif of the TRHR gene Marta Garcia Received Received
  11-7-RFC Secondary thyroid cancer among childhood cancer survivors. A single institution experience. Monica Muraca Received Received
  11-4-RFC Thyroid function in monozygotic twins with intra-twin birth-weight-differences Sandra Schulte Received Received
  11-5-RFC Novel homozygous mutation in the sodium/iodide symporter (NIS) gene highlight by next generation sequencing (NGS) in a patient with congenital hypothyroidism isabelle oliver petit Received Received
  11-P1 Evaluation of the glucocorticoid, mineralocorticoid, and adrenal androgen secretion dynamics in a large cohort of patients aged 6-18 years with transfusion-dependent -thalassemia major, with an emphasis on the impact of cardiac iron load Ahmet Uar Received Received
  12-LBP An analysis of symptoms and signs of adrenal insufficiency in children with CAH admitted to hospital in Australia. Georgina Chrisp Received Received
  12-4-RFC Molecular screening of MKRN3, DLK1 and KCNK9 genes in central precocious puberty Anna Grandone Received Received
  12-6-RFC Serum antimllerian hormone and inhibin B as potential markers for progressive central precocious puberty in girls Ting Chen Received Received
  12-8-RFC Circulating MKRN3 levels decline during puberty in healthy boys Alexander Busch Received Received
  12-5-RFC A novel MKRN3 nonsense mutation causing familial central precocious puberty Athanasios Christoforidis Received Received
  12-P1 Testicular adrenal rest tumours in 50 boys, adolescents and adult male with congenital adrenal hyperplasia Miroslav Dumic Received Received
  12-2-RFC A novel mutation of KISS1R causing a normosmic isolated hypogonadotropic hypogonadism Keisuke Yoshii Received Received
  12-7-RFC Prevalence of organic lesions in males with central precocious puberty. Stefania Pedicelli Received Received
  12-3-RFC Next Generation Sequencing and precocious puberty: a new diagnostic challenge to identify the molecular basis of complex diseases. Stefano Stagi Received Received
  13-LBP HYPERPROLACTINEMIA IN CHILDREN AND ADOLESCENTS: A REVIEW OF PATIENTS PRESENTING TO A TERTIARY CENTER IN AUSTRALIA. Komal Vora Received Received
  13-P1 Establishment of clinical and lab algorithms for the identification carriers of mutations in CYP21A2 a study of 768 children and adolescents Jakob Meinel Received Received
  13-2-RFC The use of proteomics in the assessment of health status of offspring born after intracytoplasmic sperm injection (ICSI) Ioanna Kosteria Received Received
  13-7-RFC Early-onset obesity and hyperphagia associated with defects in the GNAS gene Marta Garcia Received Received
  13-3-RFC Effects of eating rate on satiety hormones, meal enjoyment and memory for recent eating: An fMRI study Katherine Hawton Received Received
  13-4-RFC Which amount of BMI-SDS reduction is necessary to improve cardiovascular risk factors in overweight and obese children? Thomas Reinehr Received Received
  13-8-RFC Measuring subcutaneous adipose tissue using ultrasound in children Adela Chirita-Emandi Received Received
  14-P1 A unique case of dual opposing pathologies Irene Fernandez Viseras Received Received
  14-4-RFC Genetic diagnosis of congenital growth hormone deficiency by massive parallel sequencing using a target gene panel MARILENA NAKAGUMA Received Received
  14-6-RFC Effects of size at birth, childhood growth patterns and growth hormone treatment on telomere length Carolina Smeets Received Received
  14-2-RFC Contribution of GHR and IGFALS mutations to growth hormone resistance Identification of new variants and impact on the inheritance pattern Marie Legendre Received Received
  14-1-RFC Important contribution of GH, GHRHR and GHSR mutations in isolated growth hormone deficiency with a normal location of the posterior pituitary Functional characterization of new variants Enzo Cohen Received Received
  14-5-RFC Gene Expression Profiling of Children with GH Deficiency (GHD) Prior to Treatment with Recombinant Human Growth Hormone (r-hGH) is Associated with Growth Response Over Five Years of Therapy Steven Goodrick Received Received
  14-7-RFC GH influences plasma fasting adropin concentration in patients with Turner syndrome Beata Wikiera Received Received
  14-3-RFC Whole Exome Sequencing Identifies a GH1 Gene Mutation Causing Familial Isolated Growth Hormone Deficiency with Normal Peak Growth Hormone Concentrations Catalina Cabrera Salcedo Received Received
  15-7-RFC Long-term safety and effectiveness of daily and weekly growth hormone treatment in pediatric GHD patients (4-years results) Sochung Chung Received Received
  15-6-RFC Safety of GH in Paediatrics: The GeNeSIS Prospective Observational Study Experience Between 1999 and 2015 (NCT01088412) Chris Child Received Received
  15-P1 Individualized optimization with 17OHP-saliva profiles leads to changes in hydrocortisone (HC) dosing pattern in children with congenital adrenal hyperplasia (CAH) Uta Neumann Received Received
  15-2-RFC NR0B1 Frameshift Mutation in a Boy with Precocious Puberty and Normal Adrenal Function Hirohito Shima Received Received
  15-8-RFC Replacement of male mini-puberty DIMITRIOS T. PAPADIMITRIOU Received Received
  16-P1 Cortisol response to ACTH stimulation test in non-classical congenital adrenal hyperplasia (NCCAH) FENELI KARACHALIOU Received Received
  17-P1 Altered stress system activity in children with ADHD Eleni Angeli Received Received
  18-P1 Adult individuals with classic congenital adrenal hyperplasia exhibit deficits in utive functions Leif Karlsson Received Received
  19-P1 Heterozygous mutations in CYP11A1 gene can cause life-threatening salt wasting and failure to thrive DIMITRIOS T. PAPADIMITRIOU Received Received
  20-P1 Antiviral HIV treatment - a new cause of transient neonatal adrenal insufficiency Tanja Haamberg Received Received
  21-P1 Increased salivary and hair cortisol and decreased salivary alpha-amylase concentrations in obese prepubertal girls Chrysanthe Papafotiou Received Received
  22-P1 An Assessment Of The Hypothalamic-Pituitary-Adrenal Axis In Children With Prader-Willi Syndrome Andreas Kyriakou Received Received
  23-P1 The Urinary Steroidome of Children with Classic 21-Hydroxylase Deficiency Treated with Hydrocortisone Clemens Kamrath Received Received
  24-P1 Adrenal insufficiency in ROHHADNETsyndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and Neural Tumor) Ramona Tallone Received Received
  25-P1 The psychosocial impact of Adrenal Insufficiency (AI) and Congenital Adrenal Hyperplasia (CAH) on children and their parents Amy Simpson Received Received
  26-P1 Sex-specific differences in hypothalamus-pituitary-adrenal axis activity in newborns with very low birth weight Bibian van der Voorn Received Received
  27-P1 Beckwith-Wiedemann Syndrome and Bilateral Phaeochromocytoma: a Diagnostic Challenge Emily Cottrell Received Received
  28-P1 Combined glucocorticoid and mineralocorticoid deficiency related to a new NNT mutation : a case report. Emilie Doye Received Received
  29-P1 Testicular adrenal rest tumours in patient with X-linked adrenoleukodystrophy Igor Chugunov Received Received
  31-P1 Growth of children with congenital adrenal hyperplasia (CAH) during the first 2 yearsof life data from the Duth longitudinal registry. Annelieke van der Linde Received Received
  32-P1 Molecular Confirmatory Test Improves the Accuracy of Congenital Adrenal Hyperplasia Diagnosis in Newborn Screening Program Mirela Miranda Received Received
  33-P1 USEFULNESS OF CORTICOTROPIN TEST IN CHILDREN AND ADOLESCENTS WITH CLINICAL HYPERANDROGENISM FENELI KARACHALIOU Received Received
  34-P1 Primary Adrenal Insufficiency in children: results from a large nationwide cohort Martina Rezzuto Received Received
  35-P1 Follow-up of growth and puberty in children with premature adrenarche Jani Liimatta Received Received
  36-P1 Early onset hypertension with primary hyperaldosteronism through mutation in the calcium channel CACNA1H - case report. Corina Chirita Received Received
  37-P1 DNA Methylation Signatures Associated With Prenatal Dexamethasone Treatment Leif Karlsson Received Received
  38-P1 Twenty Years Experience in Congenital Adrenal Hyperplasia: Clinical, Hormonal and Molecular Characteristics in a Large Cohort Mirela de Miranda Received Received
  39-P1 Chronic adrenal insufficiency due to a mutation of Nicotinamide Nucleotide Transhydrogenase 1 (NNT1) : case report Jacques WEILL Received Received
  40-P1 Cognitive Functions in Congenital Adrenal Hyperplasia nermine amr Received Received
  41-P1 RET AND TP53 CONCOMITANT MUTATIONS: A CHALLENGING APPROACH TO A UNIQUE ASSOCIATION OF HIGH TUMOR PREDISPOSING CONDITIONS matilde calanchini Received Received
  42-P1 Acute lysis of a giant pediatric adrenal cortical carcinoma following one dose of opDDD Emmanuelle Motte Received Received
  43-P1 Severe Hypertension in a Girl: Cushing Syndrome or Apparent Mineralocorticoid Excess Syndrome? Utility of Molecular Study Cristian Seiltgens Received Received
  44-P1 An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome Glay Karagzel Received Received
  45-P1 Polymorphisms analyze in CYP21A2 gene associated with congenital adrenal hyperplasia (CAH) Cristiane Kopacek Received Received
  46-P1 The effect of intrauterine stress on leukocyte telomere length in newborns Penio Kassari Received Received
  47-P1 Predictive Factors for Premature Pubarche in a Large Cohort of Italian Children Rossella Gaudino Received Received
  48-P1 Cardiac function in pediatric patients with congenital adrenal hyperplasia Christiaan Mooij Received Received
  49-P2 Evaluation of the combination of anti-androgen and anti-estrogen treatment in classical Congenital Adrenal Hyperplasia (CAH) in boys: retrospective study of 11 cases Jacques Weill Received Received
  50-P2 Ovarian cysts in a 46,XX patient with congenital lipoid adrenal hyperplasia and with spontaneous puberty Irina Kopylova Received Received
  51-P2 Bone health index in children and adolescents with congenital adrenal hyperplasia Hussain Alsaffar Received Received
  52-P2 Occasional detection of an adrenal incidentaloma in a female adolescent evaluated for cardiac arrhythmias. Eleni P Kotanidou Received Received
  53-P2 Final height in congenital adrenal hyperplasia: a retrospective study Martins Mariana Received Received
  54-P2 Hyperandrogenism in a 12-year old girl with a congenital porto-systemic shunt and congenital hepatic fibrosis Mikolaj Danko Received Received
  55-P2 THE TREATMENT OF A FUNCTIONAL ADRENOCORTICAL CANCER WITH MITOTANE Selim Kurtoglu Received Received
  58-P2 Isthmic spondylolisthesis in a pre-pubertal boy with congenital adrenal hyperplasia during aromatase inhibitor treatment. Nadya Katherine Jaimes Fajardo Received Received
  59-P2 Hospitalisation in children with adrenal insufficiency and hypopituitarism: is there a differential burden between boys and girls and between age groups? R. Louise Rushworth Received Received
  60-P2 A Case of Cushings Syndrome due to Adrenocortical Adenoma with Pubarche and Obesity fatih gurbuz Received Received
  61-P2 Severe neonatal Cushing syndrome with multi-organ McCune Albright manifestations ANNE-SPOHIE LAMBERT Received Received
  62-P2 Final height data in a cohort of patients with Congenital Adrenal Hyperplasia treated withtailored doses of hydrocortisone Shir Wey Gloria Pang Received Received
  63-P2 The evolution of bone age in girls with premature adrenarche (PA) Anastasios Papadimitriou Received Received
  64-P2 Cushing syndrome due to adrenal adenoma in an adolescent patient and successful treatment with laparoscopic surgery Bulent Hacihamdioglu Received Received
  65-P2 A novel mutation of DAX-1 (NR0B1) in a boy with X-linked adrenal hypoplasia congenita Karine Gerster Received Received
  66-P2 CLINICAL-LABORATORY FINDINGS OF THE CASES WITH PREMATURE PUBARCHE AND THE VALUE OF ACTH STIMULATION TEST IN THE DIFFERENTIAL DIAGNOSIS Emine Dilek Received Received
  67-P2 Successful medical management of severe neonatal Cushing syndrome with metyrapone, guided by mass spectrometry monitoring Poidvin Amélie Received Received
  68-P2 FAMILY CHARACTER ISOLATED PHEOCHROMOCYTOMA BY MUTATION IN VHL GEN FREIJO CONCEPCION Received Received
  69-P2 Exaggerated adrenarche and exogenous obesity: a diagnostic challenge Beatriz Semer Received Received
  70-P2 Vitamin D insufficiency is related to premature adrenarche onur akin Received Received
  71-P2 A case of 17 years-old boy with relapsing Cushing disease presenting vertebral compression fracture Yoo-Mi Kim Received Received
  72-P2 The Impact of 21 hydroxylase deficiency on Cardiac Repolarization Changes in Children with 21-hydroxylase-deficient congenital adrenal hyperplasia Hseyin Anil Korkmaz Received Received
  73-P2 Patients with Congenital Adrenal Hyperplasia have significantly higher healthcare utilisation than the general paediatric population John Porter Received Received
  74-P2 CHOLESTASIS AND HYPERCALCEMIA SECONDARY TO PANHYPOPITUITARISM IN A NEWBORN Fatma Dursun Received Received
  75-P2 CLINICAL MANAGEMENT IN SECONDARY PSEUDOHYPOALDOSTERONISM: A CASE SERIES Ahmet Ozdemir Received Received
  76-P2 High sensitivity C-reactive protein (hsCRP) levels as predictor of salivary cortisol acute response to mental stress and/or mobile phone call in healthy adolescents Styliani Geronikolou Received Received
  77-P2 Management dilemmas in a genetically female child with congenital adrenal hyperplasia raised as a male Sumudu Seneviratne Received Received
  78-P2 Primary Pigmented Nodular Adrenocortical Disease (PPNAD) justifying a pediatric case of ACTH-independent Cushing Syndrome (CS) Cristiane Kopacek Received Received
  79-P2 Three Chinese Patients from Two Kindreds with Aldosterone Synthase Deficiency: Clinical Characteristic with Mutation Analysis Report MELATI WIJAYA Received Received
  80-P2 Addisonian crisis due to autoimmune adrenalitis in a 14 year old boy with a history of hematopoietic stem cell transplantation (HSCT). Theresa Penger Received Received
  82-P2 A novel mutation of HSD3beta2 presenting as hypospadias with salt-wasting in a male infant Charles Buchanan Received Received
  83-P2 Testicular adrenal rest tumors in two young patients with congenital adrenal hyperplasia Alina Daniela Belceanu Received Received
  84-P2 Hyperreninemic Hypoaldosteronism: clinical and genetic features in pediatric patients Stefano Stagi Received Received
  86-P2 Congenital adrenal hyperplasia revealed by adrenal nodules soumeya fedala Received Received
  87-P2 Urosepsis or Pseudohypoaldosteronism in a Neonate? Noah Gruber Received Received
  88-P2 A Case Report of Adrenocortical Adenoma in a Young Girl Huyen Tran Received Received
  90-P2 A Genetic Diagnosis Of Familial Glucocorticoid Deficiency Resulting In Cessation Of Long Term Mineralocorticoid Treatment In Three Siblings. Emily Cottrell Received Received
  91-P2 Corticosteroid-induced adrenal insufficiency in a child with T cell lymphoblastic lymphoma: A case report SangHyun Lee Received Received
  92-P2 Dilated Cardiomyopathy- A rare endocrine association with Congenital Adrenal Hyperplasia due to 11 beta hydroxylase deficiency. Prashant Patil Received Received
  93-P2 Use of an F-DEX binding assay to measure steroid responsiveness ofpatients and their related donors undergoing stem cell transplant Steven Ghanny Received Received
  94-P2 11- hydroxylase deficiency due to a novel compound heterozygous mutation and literature review Wei Wu Received Received
  97-P2 Congenital adrenal hyperplasia Subtle presentations with critical electrolyte imbalances and cardiac arrhythmias. Abirami Namasivayam Received Received
  98-P1 KNOCK IN OF THE RECURRENT R368X MUTATION OF PRKAR1A THAT REPRESSES CAMP-DEPENDENT PROTEIN KINASE A ACTIVATION : A MODEL OF ACRODYSOSTOSIS TYPE 1 Catherine Le Stunff Received Received
  99-P1 Automated Greulich-Pyle bone age determinations in children with chronic endocrine diseases Daniela Klose Received Received
  100-P1 Cord 25-hydroxy-vitamin D is not associated with cranial anthropometrics in infants. Sissil Egge Received Received
  101-P1 Effect of bisphosphonates on bone fragility due to chronic liver disease in ten children Alessia Usardi Received Received
  102-P1 Radiologically Confirmed Fractures In A Scottish Nationwide Cohort Of Boys With Duchenne Muscular Dystrophy Shuko Joseph Received Received
  103-P1 Monostotic Fibrous Dysplasia is a single disorder caused by somatic mosaic activating mutations in GNAS Hironori Shibata Received Received
  104-P1 Clinically significant fracture incidence in Czech children: a population-based study. Ondrej Soucek Received Received
  105-P1 Effects of Selective GPER-1 Agonist G1 on Bone Growth Maryam Iravani Received Received
  106-P1 Bone mineral density, pubertal status and ability to walk are associated to fracture incidence in patients with Rett syndrome. Anya Rothenbuhler Received Received
  107-P1 Bone mineral status in children and adolescents with Klinefelter Syndrome Stefano Stagi Received Received
  108-P1 Tolerability and feasibility of whole body vibration and its effects on muscle function and bone health in patients with dystrophinopathy Anna Petryk Received Received
  109-P1 Nonsense mutation in SPARC gene causing autosomal recessive ostegenesis imperfecta SAYGIN ABALI Received Received
  110-P1 Increase in sclerostin after rapid weight loss in children. Niels Birkebaek Received Received
  111-P1 Impact of conventional medical treatment on bone mineral density and bone turnover in adult XLH patients: a 6 year cohort study Signe Sparre Beck-Nielsen Received Received
  112-P1 Bone Health and Body Composition in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting Mahjouba Ahmid Received Received
  113-P1 Extension of the Bone Health Index to adults, and reference curves of four indices of cortical bone for healthy Europeans David Martin Received Received
  114-P1 Extension of automated bone age determination to the end of puberty David Martin Received Received
  115-P1 A European survey to identify new roads for care, training and research around rare metabolic bone diseases Isabelle FERNANDEZ Received Received
  116-P1 Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients Sarah Bakhamis Received Received
  117-P1 No severe hypercalcemia during a 12-month high-dose vitamin D intervention in infants Saara Valkama Received Received
  118-P1 Management of tracheobronchomalacia during asfotase alfa treatment in infants with perinatal-onset hypophosphatasia: a case series Raja Padidela Received Received
  119-P1 Novel p.Asn628Ser heterozygous mutation in FGFR1 is associated with Hartsfield syndrome and tumoral calcinosis Rathi Prasad Received Received
  120-P1 Practicalities of Bisphosphonate Use in UK Paediatric Tertiary Centres Victoria Price Received Received
  121-P1 Computer-assisted diagnosis of dyschondrosteosis based on skeletal X-ray geometry. Gianpaolo De Filippo Received Received
  122-P1 Bisphosphonates therapy in girls with Rett syndrome and bone fragility LAMBERT ANNE-SOPHIE Received Received
  123-P1 Skeletal manifestations in APECED Saila Laakso Received Received
  124-P1 TWO FRENCH FAMILIES WITH VITAMIN D DEPENDENCY RICKETS TYPE 1B HARBOR HOMOZYGOUS RECESSIVE EXPRESSION OF CYP2R1 MUTATIONS L99P and G42_L46delinsR Arnaud Molin Received Received
  125-P1 SPECTRUM OF THE GENETIC DEFECTS IN HYPOPHOSPHATEMIC RICKETS IN A GROUP OF TURKISH CHILDREN Sezer Acar Received Received
  126-P1 Impact of intercurrent illness on calcium homeostasis and hypoparathyroidism management Amish Chinoy Received Received
  127-P1 Transient pseudohypoaldosteronism and failiure to thrive in a 5-month-old infant Hae Soon Kim Received Received
  128-P1 Childhood Cancer Survivors (CCS) are at High Risk of Reduced Bone Mass during Bone Mass Accrual DI IORGI NATASCIA Received Received
  130-P1 Triple X Syndrome: An Evaluation of Bone Mineral Status and Metabolism Stefano Stagi Received Received
  131-P1 Frequency of recessive osteogenesis imperfecta in a Turkish cohort and genetic causes Saygin Abali Received Received
  132-P1 Spinal and forearm bone mineralization in adolescents with Klinefelter syndrome. jean de schepper Received Received
  133-P1 Treatment with Zoledronic Acid in children with Duchenne Muscular Dystrophy. Irene Fernandez Viseras Received Received
  135-P1 Low bone mineral density in adolescents with leukemia after hematopoietic stem cell transplantation cho wonkyoung Received Received
  136-P1 Growth characteristics of a girl with multicentric carpo-tarsal osteolysis caused by novel mutation in the MAFB gene Lenka Dusatkova Received Received
  137-P1 Treatment Experience And Long-Term Follow-up Data in Two Severe Neonatal Hyperparathyroidism Cases Senay Savas-Erdeve Received Received
  138-P1 Biochemical parameters associated with serum intact FGF23 levels in patients with X-linked hypophosphatemic rickets Takuo Kubota Received Received
  139-P1 Dental effects of intravenous bisphosphonate when administered in early infancy margaret zacharin Received Received
  140-P1 Bone mass and vitamin D status in children and adolescents with generalized epidermolysis bullosa Luiz Claudio Castro Received Received
  141-P1 Use of the aromatase inhibitor letrozole in pubertal boys to improve final height: laboratory, auxological and bone age data Carmen Sydlik Received Received
  142-P1 Effect of Bisphosphonates and Denosumab on trabecular bone: Results of a pilot study in children with Osteogenesis imperfecta. Mirko Rehberg Received Received
  143-P1 Impact Of Anti-Tumour Necrosis Factor Therapy On The Insulin Like Growth Factor Axis And Bone Development In Childhood Crohns Disease Mabrouka AlTowati Received Received
  144-P1 Effects of phylloquinone and magnesium on ATDC5 prechondrocytes Adalbert Raimann Received Received
  145-P1 To study the efficacy and safety of growth hormone (GH) therapy in children with pycnodysostosis Zainaba Mohamed Received Received
  146-P2 Bone mineral status and metabolism in patients with Williams-Beuren Syndrome Stefano Stagi Received Received
  147-P2 The beneficial effect of cinacalcet on the treatment of vitD resistant rickets Aysehan Akinci Received Received
  148-P2 A PRELIMINARY REPORT ON BODY COMPOSITION PROFILE OF YOUNG PATIENTS WITH CHRONIC HEMOLYTIC CONDITIONS. Artemis Doulgeraki Received Received
  149-P2 Bone status in a patient with IGF-I receptor deletion syndrome: bone quality and structure evaluation using DXA, pQCT, and QUS Stefano Stagi Received Received
  150-P2 Prevalence of Vitamin D Deficiency in Haitian Infants and Children Julia von Oettingen Received Received
  151-P2 Progressive development of PTH resistance in patients with maternal GNAS inactivating mutations Asmaa Mamoune Received Received
  152-P2 Effect of Hydroxyurea Therapy on Growth Parameters in Older Children with Sickle Cell Disease doaa khater Received Received
  153-P2 Evaluation of ALP value in early prediction of the effects of growth hormone treatment in children with growth hormone deficiency (GHD) Ewelina Witkowska-S&281;dek Received Received
  154-P2 Comparison of Two Different Stoss Therapy Doses in Children with Vitamin D Deficiency or Insufficiency without Rickets Cemil Kocyigit Received Received
  155-P2 Bisphosphonate Treatment of Hypercalcemia in a Child with Jansens Metaphyseal Chondrodysplasia Erin Sharwood Received Received
  156-P2 Physical exercise level is associated to peak bone mass in undergraduate students. Deisi Maria Vargas Received Received
  157-P2 A CASE WITH LETHAL PERINATAL HYPOPHOSPHATASIA SEL&304;N ELMAO&286;ULLARI Received Received
  158-P2 Anthropometric and Nutritional Parameters in Egyptian Children with Osteogenesis Imperfecta: Effect of Zoledronic Acid Therapy Rasha Hamza Received Received
  159-P2 Low bone mineral density in adolescents with joint hypermobility Shadab Salehpour Received Received
  160-P2 Fractures In Children With Type 1 Diabetes Are Associated With Poorer Bone Mineral Status and Glycaemic Control Suet Ching Chen Received Received
  161-P2 Identification of predictor factors of growth outcome in children with hypophosphatemic rickets Silvia Marin Received Received
  162-P2 Effects of different socioeconomic conditions on bone mineral density in healthy female college students; relation with vitamin D status Betul Ersoy Received Received
  163-P2 Bone health index is low in children with growth hormone deficiency and improves with growth hormone treatment Joanne Blair Received Received
  165-P2 Bone health and metabolic syndrome in childhood cancer survivors Ju Young Yoon Received Received
  166-P2 Diversity in phenotype of 2 siblings with X-linked hypophosphatemic rickets due to PHEX mutation Aleksandra Rojek Received Received
  167-P2 Expression of Brdu, VEGF, IGF-1R and change of the growth plates from sex hormone-inhibited adolescents rats- Pilot study Ji-Young Seo Received Received
  168-P2 A case of genetically proven carbonic anhydrase II deficiency Zdravka Todorova Received Received
  169-P2 RICKETS AS PRECOCIOUS SIGN OF CELIAC DISEASE: THE ROLE OF VDR POLYMORPHISMS Maria Cristina Maggio Received Received
  170-P2 Clinical and genetic analysis of five patients with vitamin D-dependent rickets type 1A Bulent Hacihamdioglu Received Received
  171-P2 about a case of a family of pycnodysostose rouabah niroud Received Received
  172-P2 Potential Role of Vitamin D in Pathogenesis of Acute Rheumatic Fever Huseyin Demirbilek Received Received
  173-P2 Bartter syndrome with bone-destroying hyperparathyroidism (BSHPT): about two cases, genetically proved, with long-lasting follow-up Jacques Weill Received Received
  174-P2 Management of Hypoparathyroidism: Follow up of 20 Patients Sukran Darcan Received Received
  175-P2 Assessing the Serum Levels of Ferritin and Selenium in three Important Infections of Childhood, Compared to a Control Group Fahimeh Soheilipour Received Received
  176-P2 A case: Hydrocephalus secondary to suprasellar arachnoid cyst with reset osmostat and Isolated Growth Hormone Deficiency Erdal Kurnaz Received Received
  177-P2 Cinacalcet Treatment in a Child With Concurrent Juvenile Idiopathic Arthritis and Hypocalciuric Hypercalcemia Bulent Hacihamdioglu Received Received
  179-P2 BISPHOSPHONATE USE FOR CONTROL OF CHRONIC SEVERE BONE PAIN IN CHILDREN WITH MALIGNANCY ASSOCIATED BONE INVOLVEMENT margaret Zacharin Received Received
  180-P2 Renal tubular acidosis causing severe growth delay and rickets in two siblings in Haiti Dearthlie Bernadea Received Received
  181-P2 PSEUDOHYPOPARATHYROIDISM TYPE Ib ASSOCIATED TO ASSISTED REPRODUCTIVE TECHNOLOGIES: CASE REPORT. Monica Fernandez Received Received
  182-P2 Primary hyperparathyroidism- a cause of metabolic syndrome in children? Amalia Ioana Arhire Received Received
  183-P2 Hyperphosphatemic familial tumoral calcinosis: novel indication to sevelamer carbonate Noemi Auxiliadora Fuentes-Bolaños Received Received
  185-P2 Multifocal osteonecrosis after short term methylprednysolon therapy:Case report Aferdita Kumaraku Received Received
  186-P2 UNCLEAR ORIGIN OF AVASCULAR NECROSIS - CLINICAL CASE Eremciuc Rodica Received Received
  187-P2 Is NOTCH- Sonic Hedgehog signalling pathway the missing link between Hajdu-Cheney syndrome and syringomyelia? Prashant Patil Received Received
  188-P2 The unexpected cause of Vitamin D deficiency in a resource limited setting; A rare case report of Primary Intestinal Lymphangiectasia Dipesalema Joel Received Received
  189-P2 about a case of dwarfism idiopathic rouabah niroud Received Received
  190-P1 The association of HLA class II, CTLA-4 and PTPN22 genetic polymorphisms and -cell autoantibodies in development of type I diabetes in patients with autoimmune thyroid disease Nataa Rojni&263; Putarek Received Received
  191-P1 Insulin pump does not allow a better control than injections in childhood type 1 diabetes in the ISIS-Diab cohort. Pierre Bougnères Received Received
  192-P1 Diagnostic features of lipodystrophy in children with type 1 diabetes Svitlana Chumak Received Received
  193-P1 Recombinant human Insulin-like Growth Factor 1 (rhIGF1) treatment of a case of leprechaunism : A two and a half year follow-up Jacques Weill Received Received
  194-P1 Longitudinal monitoring of pediatric insulin treatment in Germany and Austria: Age-dependent analysis of 63,967 children and adolescents with type 1 diabetes from the DPV registry Barbara Bohn Received Received
  195-P1 Two patients with HADH (SCHAD) hyperinsulinism without detectable 3-hydroxybutyrylcarnitine/ 3-hydroxyglutarate. Susanne Weiss Received Received
  196-P1 Development of Type 1 diabetes in a child with inherited CD59 deficiency treated with eculizumab Serkan Bilge Koca Received Received
  197-P1 Diagnosis of non-autoimmune paediatric diabetes by targeted next generation sequencing (NGS): findings in two families with rare mono- and digenic forms of diabetes Poidvin Amélie Received Received
  198-P1 NEONATAL DIABETES, GALLBLADDER AGENESIS AND CHOLESTATIC GIANT CELL HEPATITIS: A NOVEL HOMOZYGOTE MUTATION IN PDX-1 GENE Ahmet Ozdemir Received Received
  199-P1 Anthropometry and glucose homeostasis in a patient with Donohue Syndrome (homozygous insulin receptor mutation): effect of continuous subcutaneous rIGF-I therapy Michaela Plamper Received Received
  200-P1 Driving paediatric diabetes care forward in the UK: Improvements in outcomes in the North West following national initiatives Helen Moore Received Received
  201-P1 Non-surgical treatment of diazoxide-resistant of early diffuse hyperinsulinism using long-acting (LA) octreotide, a somatostatin analog: follow-up of six cases Jacques Weill Received Received
  202-P1 SCREENING FOR AUTONOMIC NEUROPATHY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS Charalampos Tsentidis Received Received
  203-P1 Diabetes Mellitus caused by bone marrow transplantation and total body irradiation experience from a regional single centre. Toby Candler Received Received
  204-P1 A syndrome of permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense c.449TA (p.I150N) mutation in NEUROD1 gene. Nihal Hatipoglu Received Received
  205-P1 Are we screening appropriate age group for early diagnosis of Cystic Fibrosis Related Diabetes (CFRD) in UK? arundoss gangadharan Received Received
  206-P1 When to screen for Coeliac disease in children with Type 1 Diabetes Mellitus: the controversy Ayo Ajanaku Received Received
  208-P1 Improvement of diabetic screening system for school children achieved by close cooperation with a local government of Atsugi city MAKI SAITO Received Received
  209-P1 Association between hypothalamus-pituitary adrenal axis activity and anxiety in prepubertal children with Type 1 diabetes Pascal Barat Received Received
  210-P1 Screening for liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis Kummer Sebastian Received Received
  211-P1 Exploration of social network, social integration, and socioeconomic status in families with young children with type 1 diabetes. Angela Galler Received Received
  212-P1 Permanent neonatal diabetes mellitus due to a novel homozygous GCK mutation in a premature baby with IUGR and its management Nirit Braha Received Received
  213-P1 The impact of diet on insulin dynamics over a 2 year period in children with a family history of obesity Melanie Henderson Received Received
  214-P1 Analysis of short-term efficacy of MiniMed 640G with SmartGuard in pediatric patients with type 1 diabetes Beatriz Villafuerte Received Received
  215-P1 Influence of -cell autoimmunity on cystic fibrosis related diabetes mellitus - a DPV registry analysis Michael Wurm Received Received
  216-P1 Thyroid and islet autoantibodies predict autoimmune thyroid disease already at diagnosis of type 1 diabetes Berglind Jonsdottir Received Received
  217-P1 Hemolysis in a girl with type 1 diabetes mellitus and glucose-6-phosphate dehydrogenase deficiency Lele Hou Received Received
  218-P1 Clinical characteristics and molecular analysis of patients with neonatal diabetes ZEHRA YAVAS ABALI Received Received
  219-P1 Impact of continuous glucose monitoring system on therapy of cystic fibrosis related diabetes in children and young adults Sladjana Todorovic Received Received
  220-P1 Effect of Allopurinol Versus Angiotensin Converting EnzymeInhibitors in Decreasing Microalbuminuria in Type 1 Diabetic Patients Nancy Elbarbary Received Received
  221-P1 Continuous glucose monitoring and hypoglycemia unawareness in children and adolescents with type 1 diabetes Damla Goksen Received Received
  222-P1 Transient, neonatal hyperinsulinemic hypoglycemia may be monogenetic, not only secondary to fetal life events Louise Olesen Received Received
  223-P1 The Relationship Between The Serum Irisin Levels And The Metabolic Control In Adolescents With Type 1 Diabetes Aysegl Yksel Received Received
  224-P1 Space-time Environmental associations in childhood type 1 diabetes (T1D). A case-control geographical approach in the ISIS-Diab cohort. Sophie Le Fur Received Received
  227-P1 Rising of type 1 diabetes mellitus incidence in Chilean children between 2006 and 2014.Final results. CAROLINA PAZ GARFIAS VON FURSTENBERG Received Received
  228-P1 Frequency and Risk Factors of Depression in Type 1 Diabetes in a Developing Country. doaa khater Received Received
  229-P1 PHENOTYPIC VARIABILITY OF IDENTICAL MUTATIONS IN THE ABCC8 GENE IN TWO FAMILIES Klara Rozenkova Received Received
  231-P1 A Rare Form of Insulin Resistance with Pseudoacromegaly Stephen Stone Received Received
  232-P1 Extrahepatic biliary atresia in combination with toxic cholestasis due to Glibenclamide in a case of neonatal diabetes Thomas Kapellen Received Received
  233-P1 HIGHER-THAN-CONVENTIONAL SUBCUTANEOUS REGULAR INSULIN DOSES FOLLOWING DIABETIC KETOACIDOSIS ARE ASSOCIATED WITH BETTER SHORT-TERM GLYCEMIC CONTROL zlem Ba&287; Received Received
  234-P1 Assessment of ed carbohydrate parameters in children exposed to gestational diabetes in utero. Ma&322;gorzata Wilk Received Received
  235-P1 The Genetic causes and Phenotypic Characteristics of Egyptian patients with Neonatal Diabetes Mellitus Rasha Elkaffas Received Received
  236-P1 Does adherence to a high HbA1c policy improve outcomes in a paediatric diabetic clinic population? Rachel Beckett Received Received
  237-P1 The prevalence of diabetic ketoacidosis in children with new-onset type 1 diabetes mellitus. Elzbieta Niechcial Received Received
  238-P1 Correction of carnitine deficiency (CD) in children with recent onset Type 1 diabetes (T1D) castell annelaure Received Received
  239-P1 Fetal growth restriction due to maternal congenital hyperinsulinism associated with a novel variant in GLUD1 and intrauterine diazoxide exposure Mirjam Dirlewanger Received Received
  240-P1 Effect of vitamin D supplementation on lipid profile in vitamin D deficient T1D patients with dyslipidemia Noha Musa Received Received
  241-P1 Renal functional reserve in children with Type 1 diabetes Vera Zdravkovic Received Received
  242-P1 The prognostic role of non-alcoholic fatty liver disease in children with type 1 diabetes mellitus with and without dyslipidemias Lusine Navasardyan Received Received
  243-P1 ASSOCIATED AND FAMILIAL AUTOIMMUNITY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1DM) Martha Papadopoulou Received Received
  244-P1 Factors affecting dyslipidaemia in children and young people with Type 1 diabetes mellitus: A multicentre study Swathi Upadrasta Received Received
  246-P1 Wolcott Rallison syndrome due to a novel mutation in EIF2AK3 gene. vikram bhaskar Received Received
  247-P1 Which is the best site for catheter placement in young children with Type 1 Diabetes (T1D) and CSII? MARIA CHATZIPSALTI (XATZIPSALTI) Received Received
  248-P1 GCK mutations in Chinese MODY2 patients: a family pedigree report and review of Chinese literature. Chunlin Wang Received Received
  249-P1 AUTOIMMUNE LIMBIC ENCEPHALITIS ASSOCIATED WITH TYPE 1 DIABETES MELLITUS esra dger Received Received
  251-P1 Metabolic impairments among adult survivors of paediatric abdominal and pelvic tumours in the St. Jude Lifetime Cohort Study Carmen Wilson Received Received
  252-P1 Clinical case of a 10-year-old girl with papillomatosis due to severe insulin resistance type A Elizaveta Orlova Received Received
  253-P1 Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome Gonul Catli Received Received
  254-P1 Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire in a case-control study Félix Balazard Received Received
  255-P1 TRANSIENT NEONATAL DIABETES MELLITUS IN HANOI, VIETNAM: CLINICAL FEATURE AND OUTCOME Ngoc CanThi Bich Received Received
  256-P1 The incidence of type 1 diabetes in the pediatric population in Pomeranian region in Poland. Agnieszka Brandt Received Received
  257-P1 Health-related quality of life and its associated factors in children with Type 1 Diabetes Mellitus Marta Murillo-Valles Received Received
  258-P1 POSSIBLE MONOGENIC DIABETES INCLUDING MODY IS HIGHLY PREVALENT IN KOREAN CHILDREN WITH DIABETES MELLITUS JungEun Moon Received Received
  259-P1 Phenotype and clinical course of diabetes mellitus in individuals with pancreatic hypoplasia due to a PTFA enhancer mutation Evangelia Panou Received Received
  260-P1 Microalbuminuria in type 1 diabetes Audit of management of children and adolescents in a single diabetes centre Aparna Kesavath Raman Nambisan Received Received
  261-P1 Johansson-Blizzard Syndrome with Pan-hypopituitrism, Type 2 Diabetes and Pancreatic insufficiency : Effect of Treatment Ashraf Soliman Received Received
  262-P2 Comparison of the occurrence of islet autoantibodies in siblings of patients with type 1 diabetes mellitus to healthy children. Joanna Sieniawska Received Received
  263-P2 The role of 24 hours ambulatory blood pressure monitoring in children and adolescents with type 1 diabetes: early experience of a single centre. Barbara Predieri Received Received
  265-P2 Efficacy and safety of Continuous Subcutaneous Insulin Infusion treatment in pre-schoolers. Long term experience of a tertiary care centre in Spain. Esmeralda Colino Received Received
  266-P2 Gene-Environment (GxE) interactions in childhood Type 1 diabetes (T1D). A case-only geographical approach in the ISIS-Diab cohort. Sophie Le Fur Received Received
  268-P2 A patient with a rare monogenic diabetes syndrome VIMAL MAVILA VEETIL Received Received
  269-P2 WHICH GROUP OF CHILDREN ACHIEVED THE BEST RESULTS DURING INSULIN PUMP THERAPY LONG-TERM OUTCOME IN CHILDREN WITH TYPE 1 DIABETES? Iwona Ben-Skowronek Received Received
  270-P2 Seasonality of type 1 diabetes in children and adolescents according to date of diagnosis and date of birth in a large diabetes centre Ioannis- Anargyros Vasilakis Received Received
  272-P2 A Case Report of Wolfram Syndrome due to a novel homozygous mutation in WFS1 gene Meltem TAYFUN Received Received
  273-P2 Lower Basal Insulin Dose - Better Control in Type 1 Diabetes David Strich Received Received
  275-P2 PANCREATIC RESERVE AND METABOLIC CONTROL OF TYPE 1 DIABETES IN A COHORT OF SPANISH CHILDREN AND ADOLESCENT MARIA LAURA BERTHOLT ZUBER Received Received
  276-P2 The Best Practice Tariff for Paediatric Diabetes Care within England: A District General Experience Kate Harvey Received Received
  277-P2 Prevalence of cardiovascular risk factors and obesity in youth with type 1 diabetes in Lithuania Ingrida Stankute Received Received
  278-P2 Childhood type 1 diabetes (T1D) management with e-learning through self-educational tools Pierre Bougnères Received Received
  279-P2 Mucormycosis and Type 1 Diabetes: A Case Report Erdal Eren Received Received
  280-P2 Insulin pump therapy in Type 1 Diabetes: The Indian experience MANPREET SETHI Received Received
  281-P2 Child with mutation in GATA 6 gene case report. Agnieszka Brandt Received Received
  282-P2 A Case Report of a 14 year old Female with a Known History of type 1 Diabetes Mellitus who Developed Tracheal Stenosis as a Result of Prolonged Intubation from Diabetic Ketoacidosis and Subsequently Developed Acute Pancreatitis Hariram Ganesh Received Received
  283-P2 Continuous glucose monitoring can alleviate parental fear of hypoglycaemia in children with type 1 diabetes mellitus. Helen Moore Received Received
  285-P2 Permanent neonatal diabetes by gene mutation kcnj11. Evolution and treatment after three years with sulphonylureas Maria Angeles Santos Mata Received Received
  286-P2 Atypical Cystic Fibrosis Adolescent Case Study (with normal sweat test) Referring with Diabetes Mellitus Symptoms Found to Carry Homozygous R352Q Mutation Mehmet Keskin Received Received
  287-P2 Diabetic ketoacidosis risk factors in the initial presentation of type 1 Diabetes mellitus in children and adolescents. Teresa Borges Received Received
  288-P2 Prevalence of polycystic ovary symdrome and its clinical profile in young females with type 1 diabetes mellitus PREETI DABADGHAO Received Received
  290-P2 Wolcott-Rallison syndrome: clinical case presentation Viktoriya Furdela Received Received
  291-P2 The story of a de novo heterozygous HNF1A mutation Abirami Namasivayam Received Received
  292-P2 Effect of packed cell transfusion on blood glucose concentrations in Beta Thalassemia Major (BTM). Ashraf Soliman Received Received
  293-P2 Impact of demographic factors on Diabetic Ketoacidosis occurrence at Type 1 Diabetes onset in childhood Flora Tzifi Received Received
  294-P2 Differences in Hba1c among different ethnicities; is it just a matter of mean glycaemia? Alessandra Cocca Received Received
  295-P2 Ischemic intestinal necrosis as a Rare Complication of Diabetic Ketoacidosis in a Child with New- onset Type I Diabetes : a Case Report Jieun Lee Received Received
  296-P2 Diabetes a rare complication of ataxic telangiectasia presenting in childhood Sereesha Veleshala Received Received
  297-P2 Clinical And Demographic Characteristics of Patients with Type 1 Diabetes Mellitus and correlation with risk factors: A South Indian Database NAGESH V.SRI Received Received
  298-P2 INSULIN RESPONSE AT STANDARD GLUCOSE LOAD IN CHILDREN WITH NORMAL, LOW AND EXCESSIVE BODY MASS Tetyana Chaychenko Received Received
  299-P2 INITIAL PRESENTATION OF SUBJECTS WITH TYPE 1 DIABETES: A CHANGE IN SPECTRUM Mathew John Received Received
  300-P2 Evaluation of the epidemiological, presenting and follow-up characteristics and their impacts on the glycemic control in a large cohort of pediatric type 1 diabetes mellitus patients from Southeastern Anatolian Region of Turkey Huseyin Demirbilek Received Received
  301-P2 HbA1C and IGF-1 levels in diabetic children treated with Vitamin D Elham Hashemi Received Received
  302-P2 LONG-TERM FOLLOW-UP OF NON-DIABETIC OBESE CHILDREN AND ADOLESCENTS TREATED WITH METFORMIN Meliksah Keskin Received Received
  303-P2 Understanding the molecular and genetic basis of complex syndromes of diabetes mellitus Melissa Riachi Received Received
  304-P2 Cardiovascular Risk and Long Term Follow-up of Turkish Children with Type 2 Diabetes: Single Center Experience AYLA GUVEN Received Received
  305-P2 Thiamine responsive megaloblastic anemia due to SLCA19A2 gene mutation: Another cause of neonatal diabetes with succcesfull switch from insulin to thiamine Serpil BAS Received Received
  306-P2 Maturity-Onset Diabetes of the Young (MODY): tracking and clinical follow-up Arthur Bezerra Received Received
  307-P2 Evaluation Of Autoimmune Thyroiditis Development On Onset And During Follow Up In Cases With Type 1 Diabetes Mellitus Dilek Emine Received Received
  308-P2 The autoimmune hypothesis for acute bilateral cataract in type 1 diabetes DIMITRIOS T. PAPADIMITRIOU Received Received
  309-P2 Clinical Characteristics of Latent Autoimmune Diabetes in Youth (Type 1.5 DM) Jeesuk Yu Received Received
  310-P2 Diabetic Ketoacidosis: Clinical features and Precipitating Factors at DEMPU Amany Ibrahim Received Received
  311-P2 Diabetes Distress in Adolescents and Young Adults with Type 1 Diabetes Ingrida Stankute Received Received
  312-P2 A NOVEL GLUCOKINASE GEN MUTATION: MODY TYPE-2 CASE Aslihan Arasli Yilmaz Received Received
  313-P2 Congenital Hyperinsulinism in a resource limited setting: Overcoming barriers towards a survival path Joel Dipesalema Received Received
  314-P2 Vitamin D levels and relations with clinical and laboratory findings in children with newly diagnosed type 1 diabetes Gulay Karaguzel Received Received
  316-P2 Cystic Fibrosis Related Diabetes Afaf AlSagheis Received Received
  317-P2 Type 1 diabetes in childhood:an 8 year experience SOTIRIA GIANNOPOULOU Received Received
  318-P2 A Rare Reason of Type 2 Diabetes: Alstrm Syndrome onur akin Received Received
  320-P2 Hyperglycaemia in a boy of 13 years old: Not always Type 1 Diabetes Mellitus. A case report Zacharoula Karabouta Received Received
  321-P2 ACHIEVEMENT OF METABOLIC PARAMETER GOALS IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES ACCORDING TO THE LATEST ADA/ISPAD STANDARDS OF MEDICAL CARE IN DIABETES IN NORTH GREECE MARIA PAPAGIANNI Received Received
  322-P2 Clinical and laboratory characteristics of children and adolescents with type 1 Diabetes Mellitus. Olcay Evliyaoglu Received Received
  323-P2 Prevalence of acute metabolic complications in children with type I diabetes admitted to the children hospital in Qazvin, Iran (2005-2014) Fateme Saffari Received Received
  324-P2 Glargine versus Detemir insulin during the Honeymoon phase in a child with type1 diabetes mellitus Ashraf Soliman Received Received
  325-P2 DIABETIC KETOACIDOSIS AND MULTIPLE ORGAN FAILURE SYNDROME: A CASE STUDY Bui Thao Received Received
  326-P2 Neonatal diabetes associated with transaminitis in a growth retarded infant Kiran Parbhoo Received Received
  327-P2 Benefits of switching insulin from twice daily to multiple daily injections on glycaemic control in children with type 1 diabetes Mellitus in Sri Lanka at the Lady Ridgeway hospital, Sri Lanka Navoda Atapattu Received Received
  328-P2 RAPID ACTING INSULIN ANALOGUE TREATMENT IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS; INSULIN GLULISINE EXPERIENCE Sevinc Odabasi Gunes Received Received
  332-P2 Evaluating the impact of the diagnosis and management of children with type 1 diabetes on parents/carers Ciara McCormick Received Received
  333-P2 Association between Socioeconomic Status and Glycemic control inType 1 Diabetes Mellitus Prashant Patil Received Received
  334-P2 Minimally invasive surgical interventions in the treatment of primary persistent hyperinsulinemic hypoglycemia of infancy. Fahimeh Soheilipour Received Received
  335-P1 Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene Johanna Knskoski Received Received
  336-P1 Polycystic Ovary Syndrome in Adolescence: new therapeutic approach with Inositol and Alpha-Lipoic Acid. maria laura iezzi Received Received
  337-P1 46,XY Partial Gonadal Dysgenesis caused by an Xp21.2 interstitial duplication that does not encompass the NR0B1 gene Ana Paula dos Santos Received Received
  338-P1 Primary Ovarian Insufficiency in Childhood Cancer Survivors: A Report from the St. Jude Lifetime Cohort Wassim Chemaitilly Received Received
  339-P1 GLOBAL AND SEXUAL QUALITY OF LIFE IN PATIENTS WITH ROKITANSKI SYNDROME : A COMPARATIVE STUDY BETWEEN SURGICAL VERSUS NON SURGICAL MANAGEMENT OF VAGINAL AGENESIS IN A FRENCH COHORT OF 130 PATIENTS maud bidet Received Received
  340-P1 Intrauterine growth restriction (IUGR) affects postnatal testis maturation in rats Valentina Pampanini Received Received
  341-P1 Global application of assessment of competencies of pediatric endocrinology fellows in the management of differences of sex development (DSD) using the ESPE e-learning.org portal. Laura Kranenburg Received Received
  342-P1 Genotype-phenotype correlation of NR5A1/SF1- mutations by functional in-vitro studies Rebekka Astudillo Received Received
  343-P1 Evolution of body composition and bone mass in transgender adolescents treated with pro- or anti-androgenic progestins. Lloyd Tack Received Received
  344-P1 Sertoli cell function during chemotherapy in pediatric patients with acute lymphoblastic leukemia (ALL). Romina P. Grinspon Received Received
  345-P1 Accuracy of pelvic MRI in evaluating internal genitalia in patients with Disorders of Sex Development Linda Mahfouz Received Received
  346-P1 Using public databases, virtual controls and geolocalization to search for Environmental correlates of Hypospadias BOUGNERES Pierre Received Received
  347-P1 The International AGD Consortium: a multi-center study of 3939 infants and children with anogenital distance measurements Marie Lindhardt Johansen Received Received
  348-P1 Silent Mutations in Exonic Region of Androgen Receptor Gene Related to Androgen Insensitivity Syndrome Rafael Loch Batista Received Received
  349-P1 Severe 5 alpha reductase 2 deficiency with aphallia is caused by p.Y91H SRD5A2 mutation and is responsive to dihydrotestosterone administration during childhood Adi Auerbach Received Received
  350-P1 Clinical history and high prevalence of gonadal tumor in 14 patients with 46 XY pure gonadal dysgenesis Claire Sechter Received Received
  352-P1 A multicenter study on long-term outcomes in 59 males with 45,X/46,XY mosaicism Marie Lindhardt Johansen Received Received
  353-P1 Familial testotoxicosis: outcome and possible relation to testicular malignancies Idske Kremer Hovinga Received Received
  354-P1 Psychological impact in young women of announcement of a utero-vaginal malformation (Mayer-Rokitansky-Kster-Hauser - MRKH syndrome) and its treatment chloe ouallouche Received Received
  355-P1 Mutations at the SF-1 ligand-binding domain can lead to different effects on DNA binding: report of two novel mutations Helena Fabbri Received Received
  356-P1 A New International Registry Highlights The Differences In Practice For Reaching A Diagnosis Of CAH On Behalf Of The I-CAH/I-DSD Registry User Group mariam kourime Received Received
  357-P1 Changes in adrenal steroids during puberty suppression and cross sex hormone treatment in gender dysphoric adolescents Sebastian Schagen Received Received
  358-P1 DO THE ANTI-MULLERIAN HORMONE LEVELS OF ADOLESCENTS WITH POLYCYSTIC OVARIAN SYNDROME (PCOS), THOSE WHO ARE AT RISK FOR DEVELOPING PCOS, AND THOSE WHO EXHIBIT ISOLATED OLIGOMENORRHEA DIFFER FROM THOSE OF ADOLESCENTS WITH NORMAL MENSTRUAL CYCLES? Senay Savas-Erdeve Received Received
  359-P1 Feasibility study for avoiding early surgery in girls with 21-hydroxylase deficiency (21OHD) Pierre Bougnères Received Received
  360-P1 A novel familial androgen receptor mutation (W752G) in complete androgen insensitivity syndrome: use of in vitro study according to the nature of amino acid substitution. franoise paris Received Received
  361-P1 Partial and mixed gonadal dysgenesis cannot be distinguished by histological picture: clinical evaluation, histological differences and long term follow up of 61 Brazilian patients. Juliana Gabriel Ribeiro de Andrade Received Received
  362-P1 Aromatase activity is disrupted by mutations in P450 oxidoreductase (POR) Shaheena Parween Received Received
  363-P1 Mosaic Xq Partial Duplication Leading to Virilisation of an Adolescent Female Elizabeth Baranowski Received Received
  364-P1 GENOTYPING PATIENTS WITH DIFFERENCES OF SEX DEVELOPMENT (DSD): 25 YEARS OF INVESTIGATION OF AN ITALIAN POPULATION OF 308 CASES (194 46,XY AND 114 46,XX) LILIA BALDAZZI Received Received
  365-P1 Functional studies of a new mutation in the LH/CG receptor gene identified in 2 sisters with 46,XY DSD Susanne Flieger Received Received
  366-P1 Consecutive lynestrenol and cross-sex hormone treatment in biological female adolescents with gender dysphoria: a retrospective analysis. Lloyd Tack Received Received
  367-P1 Ovarian reserve assessment in girls and women after hematopoietic stem cell transplantation (HSCT) treatment underwent in childhood Anna Wedrychowicz Received Received
  368-P1 Precocious/early and accelerated puberty in a boy with a homozygous R192C mutation in CYP19 (aromatase) gene Mariana Costanzo Received Received
  369-P1 Long term follow up of patients with 46,XY partial gonadal dysgenesis accordingly gender assignment Nathalia Gomes Received Received
  370-P1 45,X/46,XY chromosomal disorders of sex development. Experience from a cohort of 50 patients followed in one single institution Mariana Costanzo Received Received
  371-P1 Androgen profile differs to adults in adolescent girls with polycystic ovary syndrome (PCOS) Joanne Blair Received Received
  372-P1 Effects and Side Effects of Cyproterone Acetate alone and in combination with estrogens in male to female transgender adolescents. Lloyd Tack Received Received
  373-P1 Compound heterozygous C10orf2 mutations in a Japanese patient with 46, XX ovarian failure and deafness Keisuke Nagasaki Received Received
  374-P1 GATA transcription factors in Testicular Adrenal Rest Tumours Manon Engels Received Received
  375-P1 Can we standardize sex assignment in 45,X/46,XY mixed gonadal dysgenesis? Johanna Viau Colindres Received Received
  376-P1 Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia: A Case Report Hale Tuhan Received Received
  378-P1 Randomized controlled study comparing vitamin D and omega 3-fatty acids supplementation in adolescents with polycystic ovary syndrome Flora Bacopoulou Received Received
  379-P1 Health-related Quality of Life and Psychological Wellbeing in Adults with Disorders of Sex Development (DSD) Elena Bennecke Received Received
  380-P1 Association of Genetic Polymorphisms around the LIN28B Gene and Idiopathic Central Precocious Puberty Risks among Chinese Girls Ruimin Chen Received Received
  381-P1 Psychological Outcomes and Quality of Life of patients with non-CAH Disorders of Sex Development Nalini M Selveindran Received Received
  382-P1 Normalization of Ovulation Rate in Adolescent Girls with Hyperinsulinemic Androgen Excess Lourdes Ibañez Received Received
  383-P2 Thyroid autoimmunity in adolescent girls with polycystic ovary syndrome - pilot study. Agnieszka Zachurzok Received Received
  384-P2 The efficacy and safety of gonadotropin-releasing hormone analogue treatment to suppress puberty in gender dysphoric adolescents Sebastian Schagen Received Received
  385-P2 A familial form of DSD due to NR5A1 mutation in a father and his son Claire-Lise GAY Received Received
  386-P2 High prevalence of SGA in patients with disorders of sexual development (DSD), especially idiopathic 46,XY DSD Asmahane Ladjouze Received Received
  387-P2 Questionnaire surveys targeting Japanese pediatric endocrinologists regarding reproduction in pediatric and adolescent cancer patients Yoko Miyoshi Received Received
  388-P2 Fertility outcomes after childhood onset hypothalamic hypogonadism margaret Zacharin Received Received
  389-P2 Persistent Mullerian Duct Syndrome with transverse testicular ectopia: a novel AMH receptor mutation zlem korkmaz Received Received
  390-P2 Three Cases of NR5A1 (SF1) gene mutations in DSD patients Nadezda Raygorodskaya Received Received
  391-P2 Sertoli-Leydig Cell Tumor as a rare cause of hirsutism in a young adolescent Saskia van der Straaten Received Received
  392-P2 Identification of an AR mutation in Klinefelters Syndrome during Evaluation for Penoscrotal Hypospadias Sezer Acar Received Received
  393-P2 Assessment of sexual identity in patients with congenital adrenal hyperplasia Maryam Razzaghy-Azar Received Received
  394-P2 Duct ectasia, a rare complication of gynaecomastia Noemi Auxiliadora Fuentes-Bolaños Received Received
  395-P2 Evaluation of Anti Mullerian Hormone (AMH) assay Roche on umbilical cord blood: Determination of reference values in girls and boys newborn. Ingrid Plotton Received Received
  396-P2 Hypogonadotropic hypogonadism in a girl with 2p11.2 2q12.1 duplication Stefano Stagi Received Received
  397-P2 A nonvirilized form of classic3-hydroxysteroid dehydrogenase deficiency due to a homozygous S218P mutation in the HSD3B2 gene in a girl with classic phenylketonuria Gonul Buyukyilmaz Received Received
  398-P2 NONCLASSIC CONGENITAL ADRENAL HYPERPLASIA AND FUNCTIONAL OVARIAN HYPERANDROGENISM DIAGNOSED DURING THE TRANSITION PERIOD: DIFFERENCES IN CLINICAL, HORMONAL AND METABOLIC ASPECTS HUGO BOQUETE Received Received
  399-P2 Diagnosis of PCOS in adolescents using MRI Maxime Fondin Received Received
  400-P2 Novel CYP17A1 mutation and CYP21 mutations in two siblings Emregl Isik Received Received
  401-P2 Aetiology of 46,XY DSD in Algeria; putative modifier role of pV89L polymorphism in the SRD5A2 gene in androgen receptor mutation-negative subjects Asmahane Ladjouze Received Received
  404-P2 Case report of a girl with secondary amenorrhea associated with aurantiasis cutis Ralph Decker Received Received
  405-P2 Maternal ovarian luteoma causing complete virilization of a female fetus Carla Minutti Received Received
  406-P2 The experience of GAIA (Abuse Childhood and Adolescence Group) AOU MEYER Stefano Stagi Received Received
  407-P2 State of knowledge of late endocrinological effects of hematological patients who has undergone chemotherapy Ewa Barg Received Received
  409-P2 Analysis of clinical manifestations and gene mutations of 5a-reductase type 2 deficiency in 16 cases Lele Hou Received Received
  410-P2 Unusual differential diagnosis of Hyperandrogenism in Adolescent female treated for Polycystic Ovarian Syndrome Carolina Di Blasi Received Received
  411-P2 Phenotypic and hormonal variability in 46,XY subjects with SF-1 mutations Natacha Dillies Received Received
  412-P2 Towards the roles of Kisspeptins in the ?ontrol of Gonadotropic axis: Focus on Peripheral Signaling in Androgen-dependent Tissues in the Experimentally Induced Model Hypogonadotropic Hypogonadism in Male Rats Irina Nikitina Received Received
  413-P2 Two patients presenting the extremes of the phenotypic spectrum of 5 alfa reductase deficiency; one with at new mutation. Niels Birkebaek Received Received
  414-P2 Disorders of Sex Development 45,X/46,XY: Clinical and Laboratory Characteristics of Patients Ekaterina Sannikova Received Received
  415-P2 Reproductive function of central precocious puberty in girls: A systematic review JiHyun Kim Received Received
  416-P2 Ovotesticular Disorder of Sex Development (OT- DSD) among Egyptian DSD patients mona mekkawy Received Received
  417-P2 Cytogenetic Study of Sex Chromosomal abnormalities in Egyptian DSD patients inas Mazen Received Received
  419-P2 XLAG SYNDROME CASE ACCOMPANYING A NEW ARX MUTATION AND HAS A INTERHEMISPHERIC CYST Ahmet Ozdemir Received Received
  420-P2 Congenital adrenal lipoid hyperplasia in a 30-year-old female with a tall stature Yasunori Wada Received Received
  421-P2 ONSET OF PUBERTY IN HEALTHY BOYS IS ASSOCIATED WITH A DECREASED BMI COMPARED TO VALUES PRIOR TO THE ONSET OF PUBERTY Firdevs Bas Received Received
  422-P2 LATE CLINICAL PRESENTATION, BIOLOGICAL ASSESSMENT AND MANAGEMENT OF PAIS IN A DEVELOPING COUNTRY Daniela GORDUZA Received Received
  423-P2 SISTERS WITH 46XY GONADAL DYSGENESIS AND GONADOBLASTOMA FOTEINI PETYCHAKI Received Received
  424-P2 Follow-up to adulthood of two 46,XY siblingswith 5-alpha reductase deficiency and different sex of rearing Lyne Chiniara Received Received
  425-P2 Constitutional delay of puberty: clinical and hormonal characteristics of patients Lyubov Osipova Received Received
  426-P2 Comparison between serum vitamin D levels in precocious pubertal girls and normal girls Joon woo Baek Received Received
  427-P2 Complete virilization without salt wasting in a 7-y old Haitian child with congenital adrenal hyperplasia Billy Roosler Telcide Received Received
  428-P2 Hematocolpos revealed by non-cyclic lower-back pain in a pre-menarcheal girl Nathalie Ly Received Received
  429-P2 Novel AMH and AMHR-II Mutations in Two Egyptian Families with Persistent Mullerian Duct Syndrome aya elaidy Received Received
  430-P2 Study of Genetics of Human Disorders of Sexual Development. Research Project. Markosyan Renata Received Received
  431-P2 46XX male syndrome Markosyan R Received Received
  432-P2 45,X/47,XYY chromosomal mosaicism as a cause of 46, XY Disorder of Sex Development ANIK AHMET Received Received
  433-P2 46, XY complete gonadal dysgenesis with late diagnosis Vilhelm Mladenov Received Received
  435-P2 An Infant with 49XXXXY Syndrome; A case report from Sri Lanka. Chamidri Naotunna Received Received
  436-P2 MIXED GONADAL DYSGENESIS: Patients from Instituto da Criana, HC-FMUSP Marianna Ferreira Received Received
  438-P2 HYPOGONADOTROPIC HYPOGONADISM IN A PATIENT WITH VANISHING TESTIS SYNDROME CASE REPORT Zsuzsanna Szanto Received Received
  439-P2 17 alpha hydroxylase, 17-20 lyase deficiency, a case with hypocalcemic symptoms esra dger Received Received
  440-P2 An uncommon case of adolescent with POF. Sara Queirolo Received Received
  441-P2 Trisomy 9 Syndrome in an Infant with Ambiguous Genitalia parasto rostami Received Received
  442-P1 Placental and cord blood DNA methylation profiling in small-for-gestational-age newborns from uncomplicated pregnancies: relationship to prenatal growth and postnatal body composition Marta Díaz Received Received
  443-P1 The collapse of the BDNF/POMC system in the hypothalamus is responsible for the extreme obesity with hyperphagia observed in female heterozygous MeCP2 null mice Shota Fukuhara Received Received
  444-P1 Neonatal overfeeding alters hepatic insulin sensitivity during lactation and leads to long-term insulin resistance and fatty liver in mice: Key role of Mogat1 Ramon-Krauel Marta Received Received
  445-P1 The impact of activating PIK3CA mutations and PTEN haploinsufficiency on human adipocyte phenotype and biology Franziska Kner Received Received
  446-P1 Bioinactive leptin is not frequently detected in severe early onset childhood obesity Juraj Stanik Received Received
  447-P1 Neonatal overnutrition causes sex and age dependant long term effects on body weight, body composition and serum triglyceride and free fatty acid levels Pilar Argente Received Received
  448-P1 Laparoscopic sleeve gastrectomy in adolescents with morbid and dynamic obesity. A controlled monocentric study. Gianpaolo De Filippo Received Received
  449-P1 EFICACY, SAFETY AND METABOLIC EFFECTS OF CARBOHYDRATE RESTRICTION IN THE TREATMENT OF OBESE ADOLESCENTS Gabriel Ángel Martos-Moreno Received Received
  450-P1 SEVERE HYPERTRIGLYCERIDEMIA IN PEDIATRIC ONCOLOGY PATIENT Grau Gema Received Received
  452-P1 High predictability of impaired glucose tolerance by combining diagnostic parameters in obese children Corjan de Groot Received Received
  453-P1 The effect of subclinical hypothyroidism(SH) and treatment of SH with L-T4 on basal metabolic rate in obese children: A prospective study SERP&304;L BAS Received Received
  454-P1 INFLUENCE OF TELEVISION VIEWING DURING MEALS ON EATING PATTERNS Rosaura Leis Received Received
  455-P1 7-year follow-up of mothers from a randomized controlled trial of exercise in pregnancy and their offspring Valentina Chiavaroli Received Received
  456-P1 e-Health: A National Registry and Therapeutic Algorithm for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece Penio Kassari Received Received
  457-P1 Premature adrenarche and metabolic risk: differences by gender Veronica Mericq Received Received
  458-P1 Association of miR-34a and mir-149 with obesity and insulin resistance in obese children and adolescents Mitra Nourbakhsh Received Received
  459-P1 Erythropoietin activates classical brown adipose tissue through the erythropoietin receptor/ STAT3 pathway, improving obesity and glucose homeostasis in high fat diet-induced obese mice Kazuki Kodo Received Received
  461-P1 Adiponectin and IL-6 in simple childhood obesity with and without hepatic steatosis Stefano Stagi Received Received
  462-P1 Determinants of advanced bone age in childhood obesity Corjan de Groot Received Received
  463-P1 Exposure to Phthalates Is Associated with Overweight or Obesity in 4-Year-Old Children Jieun Lee Received Received
  464-P1 Central obesity among European preschool children: The ToyBox-Study Sonya Galcheva Received Received
  465-P1 Changes in Waist-to-Height Ratio during preschool years differ between children being obese or overweight at five years of age compared with normal-weight children Annelie Lindholm Received Received
  466-P1 Remarkable Increase In The Prevalence Of Overweight And Obesity Among School Age Children In Antalya, Turkey, Between 2003 And 2015 Gamze Celmeli Received Received
  468-P1 Association of fasting triglycerides to high-density lipoprotein ratio with risk of metabolic disorders in children Andrea Paola Rojas Gil Received Received
  469-P1 Assessment of Adherence to Mediterranean diet during a weight loss intervention in children with cardiometabolic risk Lydia Morell Received Received
  470-P1 Brain structure, utive function and appetitive traits in adolescent obesity Corjan de Groot Received Received
  471-P1 Improved Clinical and Laboratory Changes after 12 Months of Use of Metformin in Obese Insulin Resistant Children and Adolescents natalia franco Received Received
  472-P1 The assessment of lipid parameters and indicators of susceptibility to atherosclerosis in a group of pediatric patients after anticancer treatment. Ewa Barg Received Received
  473-P1 Inherited duplication (X) (p11.4) associated with obesity, autoaggressive behaviour and delayed speech development Carsten Doeing Received Received
  474-P1 Switching patients with congenital hyperinsulinism from standard octreotide to long-acting release octreotide preserves blood glucose control and improves quality of life of their caregivers Claudia Piona Received Received
  475-P1 Reduction of body mass and change in body composition of the participants of the PoZdro - Programme for Prevention of Diabetes and Civilisation Diseases by Medicover Foundation preliminary results, after the first year of interventions. Hanna Magnuszewska Received Received
  476-P1 Polysomnography in obese children with and without Prader-Willi syndrome Elena Bogova Received Received
  478-P1 BMI correlates positively with hair cortisol, whereas excessive body fat correlates positively with hair cortisol. salivary cortisol and fasting insulin concentrations in prepubertal girls Eirini Christaki Received Received
  480-P1 Associations of different appetite hormones with physical activity and cardiorespiratory fitness in adolescent boys with different BMI values Vallo Tillmann Received Received
  481-P1 The Relation of Glycaemic Variability Obtained by Continuous Subcutaneous Glucose Monitoring with IL-6 and Adiponectin Levels in Obese Children with Metabolic Syndrome and Insulin Resistance Cemil Kocyigit Received Received
  482-P1 Changes in urine and plasma metabolomics profiles after a lifestyle intervention program in obese prepubertal children. María Jesús Leal Witt Received Received
  483-P1 The Effectiveness of a Stress Management Intervention Program in the Management of Overweight and Obesity in Childhood and Adolescence Penio Kassari Received Received
  484-P1 Fetuin-A as an Alternative Marker for Insulin Resistance and Cardiovascular Risk in Prepubertal Children Yeon Joung Oh Received Received
  485-P1 What are early predictors of impaired glucose tolerance in children born SGA? Indre Petraitiene Received Received
  486-P1 Multidisciplinary Intervention Programme in Childhood Obesity - Review of Service Jeremy Jones Received Received
  487-P1 Hypercholesterolemia in childhood: how the response to diet could lead to diagnosis. Lesson from a case-report. Barbara Predieri Received Received
  488-P1 GLUCOSE METABOLISM IN CHILDREN WITH PRADER-WILLI SYNDROME (PWS): THE EFFECT OF GH THERAPY Danilo Fintini Received Received
  489-P1 Impact of a group-based treatment program on adipocytokines, oxidative status, inflammatory cytokines, and pulse wave velocity in obese children and adolescents Jeerunda Santiprabhob Received Received
  490-P2 MATSUDA INDEX IN CORRELATION WITH CLINICAL INDICATORS OF INSULIN RESISTANCE IN CHILDREN AND ADOLESCENTS PETYCHAKI FOTEINI Received Received
  491-P2 Anthropometric, biological and imagistic methods for assessing the cardiovascular risk in obese children Ramona Stroescu Received Received
  492-P2 TRENDS OF NUTRITION OF UKRAINIAN CHILDREN FROM KHARKIV REGION: TENDENCY TO OVERWEIGHT, DEHYDRATION AND IMPAIRED SOCIAL ADAPTATION Tetyana Chaychenko Received Received
  493-P2 Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents Korcan Demir Received Received
  494-P2 Comparison between CDC (Centers for Disease Control and Prevention) and Italian growth charts in the characterization of pediatric obesity Stefania Pedicelli Received Received
  495-P2 The cutoff values of indirect indices for measuring insulin resistance in Korean children and adolescents Heon-Seok Han Received Received
  496-P2 Intensive exercise intervention for long-term adolescent and young adult survivors of oncology-related cranial insult: a pilot study Shoshana Rath Received Received
  497-P2 CARDIOMETABOLIC EFFECT OF SUGAR-SWEETENED BEVERAGES REDUCTION IN OBESE CHILDREN Júlia Galhardo Received Received
  498-P2 A Comprehensive and Multidisciplinary Management Plan is Extremely Effective at Reducing the Prevalence of Overweight and Obesity in Childhood and Adolescence Penio Kassari Received Received
  499-P2 Multidisciplinary care management has a positive effect on paediatric obesity and social and individual factors are associated with better outcomes Pasal Barat Received Received
  500-P2 Prevalence and characteristics of polycystic ovary syndrome in obese adolescents Marina Ybarra Received Received
  501-P2 Efficacy of the treatment for childhood obesity in specialist care: age over 10 years at baseline and acanthosis nigricans predict a worse outcome. Marketta Dalla Valle Received Received
  502-P2 METABOLIC SYNDROME IN PREPUBERTAL OBESE CHILDREN: INCLUSION OF THE TRIGLYCERIDE/HDL RATIO AS AN ALTERNATIVE DIAGNOSTIC CRITERION CARLA BOQUETE Received Received
  503-P2 The relationship between subclinical hypothyroidism and iodine deficiency, serum leptin levels and metabolic syndrome in obese children Cemil Kocyigit Received Received
  504-P2 Analysis of circulating miRNAs in obese children born small for gestational age Maria Felicia Faienza Received Received
  505-P2 Irisin and abdominal obesity in preschool age. Mina Lateva Received Received
  506-P2 Long term outcomes after hospital based, life-style weight loss intervention during childhood Toby Candler Received Received
  507-P2 Implications of Insulin resistance in obese and overweight children: A cohort analysis Sangita Yadav Received Received
  508-P2 Effects of highly mineralized water on weight and metabolism - a randomized controlled blinded trial in a pediatric hospital staff Dagmar l Allemand-Jander Received Received
  509-P2 Which marker is the most reliable one for the detection of NAFLD in outpatient clinic? Elif zsu Received Received
  510-P2 Nonalcoholic fatty liver disease: Evolution after one year of follow-up with different therapies Maria Angeles Santos Mata Received Received
  511-P2 Lifestyle Survey of Doctors, Medical Residents and Medical Students in Latvia Jurgita Gailite Received Received
  512-P2 Weight status in children at 8 years: a prospective cohort study ISOLINA RIANO-GALAN Received Received
  513-P2 Low birth weight is not associated with increased risk of metabolic syndrome in obese children and adolescents. Elena Inzaghi Received Received
  514-P2 Prader Willi Syndrome in Brazil: 6 months follow-up in a referral center Simone Sakura Ito Received Received
  515-P2 EARLY BLOOD PRESSURE ABNORMALITIES RELATED TO CARDIOVASCULAR RISK IN OBESE CHILDREN AND ADOLESCENTS Gonzalo Herraiz Received Received
  516-P2 4G polymorphism of plasminogen activator inhibitor-1 (PAI-1), PAI-1 plasma levels, and lipid profiles in overweight/obese children and adolescents Zacharoula Karabouta Received Received
  517-P2 Polycystic Ovarian Syndrome in a population of obese adolescents Elowe-Gruau Eglantine Received Received
  518-P2 Vitamin D deficiency in obese children and the relationship with insulin resistance and Metabolic Syndrome Irene Fernandez Viseras Received Received
  519-P2 Dietary habits of children and adolescents attending an Out-patient Clinic for the Prevention and Management of Overweight and Obesity in Greece Penio Kassari Received Received
  520-P2 Preliminary findings on nutrition care competence in health care professionals using a standardized questionnaire NUTCOMP Korean version Kieun Kim Received Received
  521-P2 Construction of remote monitoring system of children with tall or short stature and overweight or poor weight gain from the elementary school health checkup data Takanori Motoki Received Received
  522-P2 The effect of demographic and lifestyle factors on one-year BMI increments in 776 Norwegian children aged 6-15 years. Hege Kristiansen Received Received
  523-P2 Body image perception changes in obese and lean children Liudmila Viazava Received Received
  524-P2 Non-alcoholic hepatic steatosis in obese children and the relationship with insulin resistance Irene Fernandez Viseras Received Received
  525-P2 Prevalence of melanocortin 4 receptor (MC4R) mutations in Turkish obese children Samim zen Received Received
  526-P2 Prevalence of Overweight and Obesity in Childrenand Adolescents in Izmir, Western Turkey ZLEM NALBANTO&286;LU Received Received
  527-P2 Evaluation of metabolic abnormalities in obese children: interest of using standardized pediatric values. Adele CARLIER Received Received
  529-P2 Insulin resistance correlates to cognitive fatigue dimensions in non-diabetic obese children Pascal Barat Received Received
  530-P2 VASCULAR ENDOTHELIAL GROWTH FACTOR AS THE PREDICTOR MICROANGIOPATHY IN OBESE AND DIABETIC CHILDREN Iwona Ben-Skowronek Received Received
  531-P2 Associations of Serum 25-Hydroxyvitamin D and Components of the Metabolic Syndrome in an Egyptian Cohort Amany Ibrahim Received Received
  532-P2 Retrospective Evaluation of The Efficiency of Metformin Therapy in Obese Children with Insulin Resistance Hale Tuhan Received Received
  533-P2 Parental obesity can trigger obesity in children shahin koohmanaee Received Received
  534-P2 Value of BMI-SDS, waist circumference-SDS and waist-to-height ratio in the identification of obese children and adolescents at an increased risk for cardio-metabolic complications Primoz Kotnik Received Received
  535-P2 Thyroid dysfunction and formation of dyslipoproteiniaemias: gender differences in children with obesity Olena Budreiko Received Received
  536-P2 How early is Insulin resistance in our Pediatric population with Metabolic syndrome Sangita Yadav Received Received
  537-P2 INSULIN RESISTANCE FOR ADOLESCENTS WITH OBESITY IN LATVIA Jurgita Gailite Received Received
  538-P2 Parental obesity can trigger obesity in children shanin koohmanaee Received Received
  540-P2 Analysing child obesity risk factors: adenotonsillectomy Corina Paul Received Received
  542-P2 Obstructive Sleep Apnea Syndrome in Early Childhood: Case Report Beatriz Semer Received Received
  543-P2 25-Hydroxyvitamin D concentrations in pubertal children with obesity Desislava Yordanova Received Received
  545-P2 Prevalence of acanthosis nigricans and related factors in Iranian Obese children fatemeh sayarifard Received Received
  546-P1 HIGHER RISK OF LOW BIRTH WEIGHT AND MULTIPLE NUTRITIONAL DEFICIENCIES IN NEONATES FROM MOTHERS AFTER GASTRIC BYPASS: A CASE CONTROL STUDY maxime gerard Received Received
  547-P1 Laboratory findings of 302 patients with hyperinsulinemic hypoglycemia at hypoglycemia Tohru Yorifuji Received Received
  549-P1 Congenital Hyperinsulinism in Infancy: The profiles of insulin secretory granules are markedly different in focal- and diffuse -cells Mark Dunne Received Received
  550-P1 Persistent ketotic hypoglycemia as an atypical presentation of heterozygous HNF4A mutation Daphné Cloutier Received Received
  551-P1 Enhanced mitochondrial densities associate with the pathobiology of -cells in Congenital Hyperinsulinism in Infancy Mark Dunne Received Received
  552-P1 Congenital Adrenal Hyperplasia Newborn Screening (CAH-NBS): Improving the Effectiveness of the Neonatal 17OH-Progesterone (N17OHP) and Serum Confirmatory Tests Daniel Carvalho Received Received
  553-P1 Neonatal diabetes in Ukraine Eugenia Globa Received Received
  554-P1 Clinical and Molecular Characteristics of Turkish Patients with Congenital Hyperinsulinism: A Single-Center Experience Melek Yildiz Received Received
  555-P1 Islet of Langerhans in Congenital Hyperinsulinism in Infancy are disrupted and with decreased expression of collagen (IV) a1 chain in basement membranes Mark Dunne Received Received
  556-P1 Pancreatic Glucagon secretion is severely impaired and Somatostatin secretion unchanged in patients with Hyperinsulinaemic Hypoglycaemia PRATIK SHAH Received Received
  557-P1 Six cases of congenital hyperinsulinism caused by mutations in MODY genes karen berthelon Received Received
  558-P1 Cerebral outcome of children with congenital hyperinsulism Annett Helleskov Received Received
  559-P1 Recognition of the fetal and perinatal features of the Prader-Willi syndrome is required to avoid delay in diagnosis Filiz Mine Cizmecioglu Received Received
  560-P1 CONGENITAL HYPERINSULINISM DUE TO COMPOUND HETEROZYGOUS MUTATIONS IN THE ABCC8 GENE: 20 YEARS EXPERIENCE OF A NATIONAL REFERRAL CENTRE Sandra Walton-Betancourth Received Received
  561-P1 A case of hyperinsulinemic hypoglycemia, associated with insulin autoimmune syndrome (IAS) in 3.5 year old girl. Elena Kuznetsova Received Received
  562-P1 Effectiveness of calcium channel blocker Nifedipine in children with Hyperinsulinaemic Hypoglycaemia due to genetically proven mutations in the ABCC8 gene MARIA GUEMES Received Received
  563-P1 Hyponatremia in infants under 100 days old: frequently overlooked and multifactorial Caroline Storey Received Received
  564-P1 Long-term effects of differences in fetal environment: endocrine influences on cognitive function and personality in teen monozygotic twins Lioba Wimmer Received Received
  565-P1 Different long-term neurodevelopmental outcomes in very preterm versus very-low-birth-weight infants Jonneke Hollanders Received Received
  566-P1 Challenging management of Costello syndrome with severe Congenital Hyperinsulinaemic Hypoglycaemia. Maria Guemes Received Received
  567-P1 Risk Factors and Clinical Features of a Large Cohort of Patients with Transient Hyperinsulinemic Hypoglycaemia. John Reed Received Received
  568-P1 A rare case of neonatal hypothyroidism Chin Kien Eyton-Chong Received Received
  569-P1 Maternal nutritional risk factors associated with neonatal hyperinsulinism Mathilde Louvigné Received Received
  570-P2 Genotype and Phenotype of 99 Vietnamese Patients with Congenital Hyperinsulinism Dung Vu Chi Received Received
  571-P2 The effects of serum insulin, leptin, ghrelin, adiponectin and resistin levels on early postnatal growth in small for gestational age newborns zerrin orbak Received Received
  572-P2 Sirolimus Therapy in Infant with Congenital Hyperinsulinemic Hypoglycemia unresponsive to diaxoside CAROLINA PAZ GARFIAS VON FURSTENBERG Received Received
  573-P2 IPEX SYNDROME CAUSED BY A NOVEL MUTATION IN FOXP3 GENE: A CASE REPORT Ngoc CanThi Bich Received Received
  574-P2 Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Sensitivity in Premature Neonates Steven Ghanny Received Received
  575-P2 Persistent Hyperinsulinemic Hypoglycemic Of Infancy (PHHI) Omalmir Fathalla Received Received
  576-P2 The Postnatal Effect of Serum Vitamin D Binding Protein on Serum Vitamin D Level Hakan Dneray Received Received
  577-P2 ENDOCRINOLOGISTS HAVE A ROLE IN MODERATING ADVERSE METABOLIC CONSEQUENCES OF EARLY OVER FEEDING OF CHILDREN BORN IUGR Margaret Zacharin Received Received
  578-P2 Primary hyperparathyroidism in children and adolescents: About a series of 10 patients soumeya fedala Received Received
  579-P2 The effects of serum leptin, ghrelin, adiponectin and resistin levels on early postnatal growth in infants of diabetic mothers zerrin orbak Received Received
  580-P2 NEWBORNS OF MOTHERS AFFECTED BY AUTOINMUNE THYROID DISEASE María Magdalena Hawkins Received Received
  582-P2 BIRTH CHEST CIRCUMFERENCE RELATIONS TO CIRCULATING INSULIN-LIKE GROWTH FACTOR-I IN THE NOT-LIFE-THREATENED NEWBORN: RELEVANCE OF BIRTHWEIGHT TO BIRTH CROWN-HEEL LENGTH RATIO BEYOND THE PRESENCE OF A SMALL BIRTHWEIGHT FOR GESTATIONAL AGE AND RESPIRATORY Cesare Terzi Received Received
  583-P2 Neonatal failure to thrive not always a congenital adrenal hyperplasia. Laura Kasongo Received Received
  584-P2 A UNIQUE IL2RA MUTATION PRESENTING AS NEONATAL DIABETES, CONGENITAL HYPOTHYROIDISM AND SEPSIS SRINAGESH V Received Received
  585-P2 Change level of TRAb in newborn leads to thyroid dysfunction - case report Beata Sawicka Received Received
  586-P2 Hyperthyrotropinemia of the preterm newborn: treat or not to treat? Serena OSSOLA Received Received
  587-P2 Permanent neonatal diabetes mellitus due to a G32S heterozygous mutation in the insulin gene ke Huang Received Received
  588-P2 Case report on hyperinsulinism/hyperammonaemia (HI/HA) syndrome: an easily treatable cause of postprandial hypoglycaemia Sumudu Seneviratne Received Received
  589-P2 Severe Systemic Pseudohypoaldosteronism Type 1: 5 years of evolution Maria Miguel Gomes Received Received
  590-P2 BIRTH CHEST CIRCUMFERENCE RELATIONS TO CIRCULATING INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3 IN THE NOT-LIFE-THREATENED NEWBORN: RELEVANCE OF BIRTHWEIGHT TO BIRTH CROWN-HEEL LENGTH RATIO AFTER CONTROL FOR A SMALL BIRTHWEIGHT FOR GESTATIONAL AGE, Cesare Terzi Received Received
  592-P2 Neonatal hyperparathyroidism with homozygous missense mutation in the CASR gene Nadia Alghazir Received Received
  593-P1 The mechanistic role of Fibroblast growth factor 21 (FGF21) in Growth Hormone resistance secondary to chronic childhood conditions. Jayna Mistry Received Received
  594-P1 Somapacitan, a once-weekly reversible albumin-binding growth hormone (GH) derivative, is well tolerated and convenient in adults with GH deficiency (AGHD): results from a 26-week randomised, controlled phase 3 trial Liz Bullock Received Received
  595-P1 The diagnostic value of IGF-II, IGF-I and IGFBP-3 in Silver-Russell syndrome Gerhard Binder Received Received
  596-P1 Functional in vitro characterization of two novel germinal STAT3 mutations associated with short stature, immunodeficiency and autoimmune disease. Mariana Gutierrez Received Received
  598-P1 Human Phase1 clinical data of ALT-P1 (hGH-NexP) by Healthy Korean males. Soon Jae Park Received Received
  599-P1 Validation of prediction models for near final adult height in children with idiopathic growth hormone deficiency treated with growth hormone for 1 year. Saartje Straetemans Received Received
  600-P1 The influence of recombinant human growth hormone treatment on very small embryonic/epiblast-like stem cells (VSELs) Anna Wedrychowicz Received Received
  601-P1 A LIPID BASED SYSTEM FOR THE ORAL DELIVERY OF GROWTH HORMONE Klaus Hartmann Received Received
  602-P1 Prediction of first year response to growth hormone treatment in neural network models Urszula Smyczynska Received Received
  603-P1 Pediatric Phase 2 Data Demonstrate That TransCon hGH Has an Anti-hGH Immunogenic Profile That Is Comparable to Daily hGH David Gilfoyle Received Received
  604-P1 The exon3-deleted GH Receptor Gene polymorphism (d3-GHR) is associated with glucose metabolism and spontaneous growth but not fat mass in prepubertal short SGA children (NESGAS) Mathilde Gersel Wegmann Received Received
  605-P1 A new case of intragenic deletion in IGF1R with very mild phenotype Ruggero Coppola Received Received
  606-P1 The role of IGF-1R gene polymorphisms with regard to susceptibility to Idiopathic short stature risk in the Chinese population of Jiangxi area YANG YU Received Received
  608-P1 Pubertal Height Gain in Females with Isolated Growth Hormone Deficiency Treated with rhGH alone or in combination with GnRHan Voutetakis Antonis Received Received
  609-P1 Cognitive Abilities and Academic Achievement Among Youths With Short Stature Receiving Growth Hormone Therapy David Sandberg Received Received
  610-P1 ONE YEAR USE OF ANASTRAZOLE IMPROVES THE PREDICTED ADULT HEIGHT OF MALE ADOLESCENTS WITH AND WITHOUT ASSOCIATED GH THERAPY RENATA MACHADO PINTO Received Received
  611-P1 IGFALS Gene Deletion in a Family with Short Stature Belma Haliloglu Received Received
  612-P1 Adherence with Twice-Monthly, At-Home Dosing Schedule of Somavaratan (VRS-317) Long-Acting Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD) (NCT02068521) Ingrid Koo Received Received
  613-P1 Glucose dysregulation in children with growth hormone (GH) deficiency (GHD), Turner syndrome (TS) or born small for gestational age (SGA) treated with GH: a report from the NordiNet International Outcome Study (IOS) Liz Bullock Received Received
  614-P1 Serum alpha-klotho levels are not informative for the evaluation of GH secretion in short children. Cristina Meazza Received Received
  615-P1 Immunogenicity Results of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): A Phase 2 Study in Children with Growth Hormone Deficiency Gili Hart Received Received
  616-P1 SERUM IGF-I, IGFBP-3 AND ALS CONCENTRATIONS AND PHYSICAL PERFORMANCE IN YOUNG SWIMERS DURING A TRAINING SEASON Carlos Martinelli Received Received
  617-P1 The blood antioxidant system in adult growth hormone deficient patients after concluded childhood growth hormone therapy Maria Vorontsova Received Received
  618-P1 Design and Clinical Development of TransCon Growth Hormone for Growth Hormone Deficiency Yi Su Received Received
  619-P1 Mutations in PROP1 gene in combination with 47, XYY karyotype: case report Diliara Gubaeva Received Received
  620-P1 Efficacy of Growth Hormone Treatment in Patients with type 1 Diabetes mellitus and Growth Hormone Deficiency Ferah Aydin Received Received
  621-P1 Final height after growth hormone treatment in children with chronic renal failure Carla Bizzarri Received Received
  622-P1 Major Plasma Carotenoids Levels in Growth Hormone Deficient Children Maria Pankratova Received Received
  623-P1 Autosomal Dominant Growth Hormone Deficiency due to a novel mutation in the gh1 gene. Bradley Miller Received Received
  624-P1 A Novel GH1 Mutation in a Family with Autosomal-Dominant Type II Isolated Growth Hormone Deficiency fatih gurbuz Received Received
  625-P1 Year 2 Pharmacokinetic and Pharmacodynamic Modeling of Long-Acting Human Growth Hormone (MOD-4023) in Growth Hormone Deficient Children Gili Hart Received Received
  626-P1 Significance of IGF-I generation test in diagnosing primary and non-primary IGF-I deficiency clinical considerations Joanna Smyczynska Received Received
  627-P1 Change of growth pattern and thickness of epiphyseal plate in female rats according to injected estrogen dosage. ByungHo Kang Received Received
  628-P1 Height Gain and Safety Outcomes in Growth Hormone (GH)-Treated Girls and Boys with Idiopathic Short Stature (ISS): Experience from the Prospective GeNeSIS Observational Study Chris Child Received Received
  629-P1 Treatment of resistant paediatric somatotropinomas due to AIP mutation with Pegvisomant margaret Zacharin Received Received
  630-P1 GH-pattern with high trophs are often found after daily sc rhGH-injection in children. Elena Lundberg Received Received
  631-P1 Are the GH treatment doses in use within secretion rates of healthy children? Elena Lundberg Received Received
  632-P1 The influence of Growth Hormone treatment on Fat-free Mass in Kabuki Syndrome children. Robin Remmel Received Received
  633-P1 Evaluation of prepubertal patients with suspected neurosecretory dysfunction of growth hormone secretion: diagnostic steps and treatment response Carmen Sydlik Received Received
  634-P1 Four-year results from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope in children requiring growth hormone treatment Fiona Goodwin Received Received
  635-P1 Glucagon versus clonidine stimulation for testing growth hormone secretion in children and adolescents: which is better? Galit Asher Received Received
  636-P1 The use of Tissue Doppler Imaging in assessing right and left ventricle diastolic function in children with growth hormone deficiency before and after one-year therapy with growth hormone Randa Khalaf Received Received
  637-P1 Diagnosing GH deficiency in children by arginine hydrochloride infusion test: relationship between auxiological characteristics, arginine plasma profile and arginine-stimulated GH release Joachim Woelfle Received Received
  638-P1 Retrospective analysis of growth hormone (GH) treatment results in children with idiopathic growth hormone deficiency (IGHD), Turner Syndrome (TS) and Small for Gestational Age (SGA) using iGRO in a Pediatric Endocrine Practice. Carl-Joachim Partsch Received Received
  639-P1 Spanish ECOS Study Analysis: Socioeconomic Data, Adherence and Growth Outcomes with Case Studies Steven Goodrick Received Received
  640-P1 Analysis of correlation between stem cells (CD133/CD45 and CD133/CD45-) and anthropometric parameters of children with growth hormone/primary insuline like growth factor 1 deficiency Beata Sawicka Received Received
  641-P2 Hypochondroplasia (HC) treatment with Growth hormone (rGH). Actualization of pilot observations. Pierre Bougnères Received Received
  642-P2 The influence of Growth Hormone treatment on the Basal Metabolism in Kabuki Syndrome children. Robin Remmel Received Received
  643-P2 An analysis of the safety of childhood growth hormone (GH) therapy: data from the NordiNet International Outcome Study (IOS) Liz Bullock Received Received
  644-P2 Adverse effects after priming with testosterone in short-statured boys before growth hormone stimulation test. Andrea Albrecht Received Received
  645-P2 Effect of One-Year Growth Hormone Therapy on Serum levels of Ghrelin and Leptin in Children with Growth Hormone Deficiency and their Correlations with Cardiac Functions and dimensions Randa Khalaf Received Received
  646-P2 Metabolic Parameters and Glucose Homeostasis in in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting Mahjouba ahmid Received Received
  647-P2 Final adult height (FAH) in patients with PROR -1 gene mutations during growth hormone long-term therapy. Elena Nagaeva Received Received
  648-P2 Congenital hypopituitarism: Genotypic-phenotypic-neuroradiological correlation Cristina Partenope Received Received
  649-P2 A case of hypopituitarism in a patient with Cantù syndrome Stefano Stagi Received Received
  650-P2 Delaying puberty with GnRHa does not promote adult height in GH treated children who enters puberty at average age. PETER BANG Received Received
  651-P2 ESTIMATION OF FGF21 CONCENTRATION IN PREPUBERTAL CHILDREN WITH GROWTH HORMONE DEFICIENCY BEFORE AND AFTER 6 MONTHS OF GROWTH HORMONE TREATMENT Agnieszka Rudzka-Kocjan Received Received
  653-P2 Improving the gold standard. The insulin tolerance test revisited. Nikolaos Daskas Received Received
  654-P2 Adherence to growth hormone therapy: comparison of electronic auto-injection to non-electronic injection devices Klaus Hartmann Received Received
  655-P2 Factors influencing peak GH response during insulin and clonidine stimulation tests Ionela Pascanu Received Received
  656-P2 Improved growth outcomes with jet delivery of growth hormone in children are maintained over long-term treatment. Maria Michaelidou Received Received
  657-P2 Septo-optic dysplasia and excellent growth with low Growth Hormone dose: our experience Cristina Partenope Received Received
  658-P2 Early diagnosis and treatment of a newborn with POU1F1 mutation Thérèse Bouthors Received Received
  659-P2 Influences of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on 1 year follow-up outcome of growth hormone treatment in Korean children with growth hormone deficiency Joon woo Baek Received Received
  661-P2 First do no harm: growth hormone (hGH) treatment in a case of recurrent craniopharyngioma. George-Sebastian Zmau Received Received
  662-P2 High efficacy growth hormone therapy in patient with homozygous mutation in growth hormone gene (GH-1) during 3 years. Anna Gavrilova Received Received
  663-P2 A case of GH deficiency in a female with 3M syndrome Stefano Stagi Received Received
  664-P2 Case report of SHOX gene haploinsufficiency diagnosed in early infancy Dario Gallo Received Received
  665-P2 Association between IGF-1 (Insulin-like Growth Factor) SD levels and children with Growth Hormone Deficiency(GHD) with and without pituitary morphological abnormalities. Maria Claudia Schmitt-Lobe Received Received
  666-P2 USEFULNESS OF GROWTH HORMONE TRANSIENT TREATMENT SUSPENSION IN PREPUBERTAL CHILDREN TREATED WITH GROWTH HORMONE María Martinez Received Received
  667-P2 Birth length, weight and head circumference of neonates with IGF-I receptor mutations Zvi Laron Received Received
  668-P2 A rare cause of growth delay- Jacobsen syndrome Georgiana Constantinescu Received Received
  669-P2 A GH-1 mutation diagnosed in a preadolescent obese girl with only mild reduced height Agnès Béreau Received Received
  670-P2 A New Reusable Manual Pen Device for Injection of Human Growth Hormone (GH): Results of a Convenience and Functionality Evaluation Study David Candlish Received Received
  671-P2 Assessing Disease and Treatment Burden for Young Children with Growth Hormone Deficiency (GHD) Jane Beck Received Received
  672-P2 Long-term results of GH therapy in GH-deficient children treated in Albania Agim Gjikopulli Received Received
  676-P2 Is the growth hormone deficiency the cause of short stature in Floating Harbor syndrome? Alice Ioana Albu Received Received
  677-P2 LHX-4 Gene Mutation in a Boy with Hypopituitarism and Severe Congenital Myopathy Zoran Gucev Received Received
  679-P2 Association between growth hormone peak at a stimulation test and pituitary morphological abnormalities in children with growth hormone deficiency(GHD) Maria Claudia Schmitt-Lobe Received Received
  680-P2 A case of Growth Hormone deficiency with combined Encephalocraniocutaneouslipomatosis(ECCL) and Jaffe-Campanacci syndrome (JCS) Choi Eunmi Received Received
  681-P2 Evaluation of Growth Hormone Deficient pre pubertal children treated with Omnitrope using the AuxoLog computer program Margarida Vasconcelos Palla Garcia Received Received
  682-P2 Calcaneal Apophysitis (Severs Disease) Development in a Case Using Growth Hormone Erdal Kurnaz Received Received
  683-P2 Bone Health Index: a potential discriminator between Growth Hormone Deficiency and Constitutional Delay in Growth and Puberty in adolescent children. Prashant Patil Received Received
  684-P2 Growth effects of somatropin during the treatment congenital hypopituitarism in children after the start of puberty. Olga Berseneva Received Received
  685-P2 Congenital Hypopituitarism and Giant Cell Hepatitis in a Two-Months-Old Boy. Yulia Skorodok Received Received
  686-P2 Neonatal characteristics of GH deficiency in 107 children soumeya fedala Received Received
  687-P2 Diagnostic Value of Growth Hormone Stimulation Test for Growth Hormone Deficiency in Short Children Jeesuk Yu Received Received
  688-P1 Thyrotoxicosis, nephrogenic syndrome of inappropriate antidiuresis, tall stature and mental retardation caused by a novel GNAS gain of function mutation Muriel HOUANG Received Received
  689-P1 Novel germline mutations in DICER1 gene in patients with different pediatric hereditary tumors. Roxana Marino Received Received
  690-P1 Fludrocortisone- a treatment for tubulopathy post paediatric renal transplantation: A Scottish study Salma Ali Received Received
  691-P1 Neonatal diabetes and congenital hypothyroidism, a rare condition: report of 2 cases with different genetic causes. Carolina Mendoza Fuentes Received Received
  692-P1 Access to Medicines in Pediatric Endocrinology and Diabetes in Africa: Insights from the WHO and National Lists of Essential Medicines Amanda Rowlands Received Received
  693-P1 IS IT CAUTIOUS TO WAIT FOR SERUM BASAL CALCITONIN LEVELS RISE IN PATIENTS WITH RET CODON C634 MUTATIONS? Esther Gonzálezz Received Received
  695-P1 CANDLE syndrome a new autoinflammatory lipodystrophic disorder with challenging diagnosis and limited therapeutic options Veselin Boyadzhiev Received Received
  696-P1 Variable phenotype and genetic findings in a cohort of patients with pseudohypoparathyroidism Nadezhda Makazan Received Received
  697-P1 Contiguous gene syndrome involving NR0B1 (DAX1) deletion with congenital adrenal insufficiency Roschan Salimi Dafsari Received Received
  698-P1 Clusters of Autoinmune Diseases in Children Cristian Seiltgens Received Received
  699-P1 Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity Cristian Seiltgens Received Received
  700-P2 Effects of growth hormone treatment on glucose tolerance in young adults with Prader-Willi syndrome Stephany Donze Received Received
  701-P2 TPIT mutation may be involved in multiple pituitary deficiencies Pauline Degand Received Received
  703-P2 French National Healthcare Network for Rare Endocrine Diseases (FIRENDO): the first year of activity to monitor patients with rare endocrine diseases Maria Givony Received Received
  704-P2 Autoimmune diseases and metabolic outcome in Turner syndrome comparison between 45,X0 and other X chromosome abnormalities Yael Lebenthal Received Received
  705-P2 Endocrinological Disorders in children with Neurofibromatosis type 1 and Optic Pathway Gliomas raffaella nacca Received Received
  706-P2 Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) managed with fluid restriction and salt supplementation Lisa Amato Received Received
  707-P2 The Triglyceride to High-Density Lipoprotein Cholesterol Ratio and Non-High-Density Lipoprotein Cholesterol Reference Data for Korean Children and Adolescents: Results of the 2007-2013 Korean National Health and Nutrition Examination Surveys (KHANES) Min Jae Kang Received Received
  708-P2 Inhibition of NAMPT increases the sensitivity of leukemia cells for etoposide Theresa Gorski Received Received
  709-P2 Neonatal Endocrinological Problems In Collodion Babies Ahmet Ozdemir Received Received
  710-P2 Endocrine dysfunction in children and adolescents with CHARGE syndrome Jin-Ho Choi Received Received
  711-P2 Growth and pubertal patterns in young survivors of childhood acute lymphoblastic leukemia SHLOMIT SHALITIN Received Received
  712-P2 Clinical assessment of hypercalciuria and hypomagnesemia in patients with Bartter syndrome and Gitelman syndrome Wenjing Li Received Received
  713-P2 Wolfram syndrome: Three cases Ilkin Majidov Received Received
  714-P2 Autoimmune hypoparathyroidism and celiac disease: a rare paediatric association outside an Autoimmune Polyglandular Syndrome Francesco Gallo Received Received
  716-P2 ENDOCRINE DISORDERS IN CHILDREN WITH THALASSEMIA MAJOR A HOSPITAL BASED RETROSPECTIVE STUDY Swati Kanodia Received Received
  717-P2 15-year old girl with APS type IIIc, with post-thymectomy remission case report. Artur Bossowski Received Received
  718-P2 Endocrine and Metabolic Evaluation of Children with Neurodevelopmental Disability giorgiana brad Received Received
  720-P2 Familial Williams Syndrome Pinar Isguven Received Received
  721-P2 Stanazolol Abuse: Diagnostic Dilemma in an Adolescent with Persistent Hypoglycemia Ahmet UAR Received Received
  722-P1 Role of the metabotropic mGlu5 glutamate receptor in the initiation of puberty and reproduction in female mice Ioana Inta Received Received
  723-P1 Effect of dietary control on pubertal onset and immunoreactivity of Kisspeptin and Neurokinin B in female offspring rats fed high fat diet during perinatal period Eun Young Kim Received Received
  724-P1 Estimating the psychosocial impact of idiopathic central precocious puberty (ICPP) in girls aged 6 to 8 years: a qualitative study. Dominique Simon Received Received
  725-P1 Metabolic and Pubertal Alterations in Children with Narcolepsy-Cataplexy. carine villanueva Received Received
  726-P1 TIME COURSE OF CENTRAL PRECOCIOUS PUBERTY DEVELOPMENT CAUSED BY AN MKRN3 GENE MUTATION: A PRISMATIC CASE Monica Stecchini Received Received
  727-P1 Changes of Serum AMH and Inhibin B levels in Girls with Central Precocious Puberty before and during Treatment with GnRH Agonists Yeon Joung Oh Received Received
  728-P1 FGFR1 loss-of-function mutations of in three Japanese patients with isolated hypogonadotropic hypogonadism and split hand/foot malformation Kohnosuke Ohtaka Received Received
  729-P1 Clinical and mutational spectrum in Slovenian patients with hypogonadotropic hypogonadism Magdalena Avbelj Stefanija Received Received
  730-P1 MKRN3 mutations and Central Precocious Puberty Meropi Toumba Received Received
  731-P1 PRECOCIOUS PUBERTY IN PATIENTS WITH PRIMARY ADRENAL INSUFFICIENCY DUE TO MELANOCORTIN RECEPTOR 2 MUTATION Firdevs Bas Received Received
  732-P1 Association between estrogen receptor gene polymorphisms and premature thelarche Jong Seo Yoon Received Received
  733-P1 The influences of circulating leptin, kisspeptin, and neurokinin B levels to precocious puberty in obese girls Min Jae Kang Received Received
  734-P1 Pseudopuberty in a young girl with Adrenocortical Carcinoma during Mitotane therapy. Romana Marini Received Received
  735-P1 Prolactinomas in Children and Young Adults: 10 year experience in a Tertiary Regional Paediatric -Young Adult - NeuroEndocrine Surgical Centre Charles Buchanan Received Received
  736-P1 Cut-off values for nocturnal salivary testosterone to enable detection of early puberty Linda van der Sande Received Received
  737-P1 Title: Screening of PROP-1, LHX2 and POU1F1 mutations in patients with ectopic posterior pituitary gland Hseyin An&305;l Korkmaz Received Received
  738-P1 Oxytocin deficiency is associated with hyperphagia and weight gain in hypothalamic and common obesity: a first-in-humans proof-of-concept study Hoong-Wei Gan Received Received
  740-P1 STANDARD TRIPTORELIN THERAPY MAY NOT FULLY SUPPRESS PUBERTAL PROGRESS IN ADOLESCENTS WITH GENDER DYSPHORIA Gary Butler Received Received
  741-P1 Serum anti-mullerian hormone levels in precocious puberty girls according to the timing of GnRH agonist treatment Hyo-Kyoung Nam Received Received
  742-P1 PRECOCIOUS PUBERTY IN SEPTO-OPTIC DYSPLASIA SYNDROME PRESENTATION OF 2 CASES. Elzbieta Marczak Received Received
  743-P1 Proton therapy as a new therapeutic option for children with aggressive and not controlled macro adenoma: about 1 case. isabelle oliver petit Received Received
  744-P1 A Prospective Evaluation Of Urinary Gonadotrophins For Assessment And Management Of Pubertal Disorders Laura Lucaccioni Received Received
  745-P1 Constitutional delay of puberty or hypogonadotropic hypogonadism: diagnostic value of inhibin B and AMH measurements. Sibel Istanbullu Received Received
  746-P1 Prognostic significance of the proliferative index Ki67 for patients with craniopharyngiomas. El&380;bieta Moszczy&324;ska Received Received
  747-P1 Etiology, differential diagnosis and clinical course of delayed puberty: a single center experience Tero Varimo Received Received
  748-P1 GH therapy assessment in GH deficient patients during the transition period Amina BOUNAGA Received Received
  750-P1 Personalized health care: Home POCT sodium measurement in diabetes insipidus centralis in a patient with impaired thirst perception Annelieke van der Linde Received Received
  751-P1 Transcriptional Basis of Idiopathic Central Hypogonadism in Isolated Congenital Cryptorchidism with Defective Mini-Puberty Faruk Hadziselimovic Received Received
  752-P1 A novel MKRN3 frameshift mutation in a Bulgarian girl with central precocious puberty Mihaela Dimitrova-Mladenova Received Received
  753-P1 The intra- and inter-user reliability of Testicular Volume estimation a simulation study. Ladan Akbarian-Tefaghi Received Received
  754-P1 The metabolic negative effect of gonadotropin-releasing hormone agonist therapy in childhood: is it short-term and reversible? Barbara Predieri Received Received
  756-P1 -hCG from an occult source causing Peripheral Precocious puberty: identification of the tumour 6 years after presentation Azad Ekberzade Received Received
  757-P1 Silent corticotroph adenoma with adrenocortical choristoma in an 11-years old boy Oya Ercan Received Received
  758-P2 Clinical symptoms, Endocrine dysfunction and Radiologic findings in children with Rathkes Cleft cyst Jo Eun Jung Received Received
  759-P2 A CASE OF CENTRAL PRECOCIOUS PUBERTY IN A PATIENT WITH PRADER-WILLI SYNDROME Maria Chiara Pellegrin Received Received
  760-P2 IS AMH LEVEL DIAGNOSTIC FOR PREMATURE TELARCHE, PREMATURE ADRENARCHE AND CENTRAL PRECOCIOUS PUBERTY? Senay Savas-Erdeve Received Received
  761-P2 Paediatric Cushing Disease: one patients path to cure Galina Yordanova Received Received
  762-P2 Recovery of hypothalamic pituitary function after stalk transection and panhypopituitarism in an adolescent margaret Zacharin Received Received
  763-P2 A novel CHD7 mutation in an adolescent presenting with pubertal and growth delay MARIA-CHRISTINA ANTONIOU Received Received
  764-P2 Kallmann Syndrome due to a homozygous missense c.217CT (p.R73C) mutation detected in the exon-2 of the PROK2 gene Huseyin Demirbilek Received Received
  765-P2 Symptomatic Rathke cleft cyst in pediatric patients - clinical presentations, surgical treatment and postoperative outcomes - an analysis of 38 cases Monika Prokop Received Received
  766-P2 Congenital craniopharyngioma: report of two cases Agnieszka Bogusz Received Received
  767-P2 Congenital hypopituitarism in a patient with 18p- syndrome Anna Bolmasova Received Received
  768-P2 10 years review of endocrine diseases in Spanish patients diagnosed with primary brain tumors in a tertiary hospital. Rica Itxaso Received Received
  769-P2 Novel uses of psychiatric drugs to treat hypothalamic obesity Maria Cristina Azcona Received Received
  770-P2 POSTOPERATIVE WATER AND ELECTROLYTE DISORDERS AND AFFECTING FACTORS IN CHILDREN WITH INTRACRANIAL TUMORS esra doger Received Received
  771-P2 Compound heterozygosity for two novel POU1F1 mutations in siblings with isolated childhood onset Growth Hormone Deficiency (CO-GHD) Mariana Grace Received Received
  772-P2 Brain MRI in evaluation of endocrine diseases of childhood : causal and incidental lesions Emilie SELBONNE Received Received
  773-P2 Primary thirst defect is a rare but important complication following surgery for hypothalamic hamartoma and intractable epilepsy Giri Dinesh Received Received
  774-P2 Insulin Sensitivity in Girls with Central Precocious Puberty at Diagnosis and at 6 Months of GnRH Analogue Treatment Andrea Arcari Received Received
  775-P2 Effect of Gonadotropin Releasing Hormone Analogues on Final Height in Girls with Borderline Early Puberty or Normal Physiological Puberty Depend on Bone Age Advancement and Predicted Height Zeynep Hizli Received Received
  776-P2 Central nervous system abnormalities on brain magnetic resonance imaging among 200 Korean Girls with central precocious puberty Shin-Hee Kim Received Received
  777-P2 Impaired growth hormone secretion associated with large hypothalamic hamartoma Elena Sukarova-Angelovska Received Received
  778-P2 Comparison of triptorelin versus leuprolide in treatment of girls with central precocious puberty Glay Can Yilmaz Received Received
  779-P2 Central precocious puberty in a female with gonadal dysgenesis and bilateral gonadoblastoma Stefano Stagi Received Received
  780-P2 Precocious puberty: a single academic center experience Heta Huttunen Received Received
  781-P2 Does Pituitary Volume Based on Bone Age Have the Diagnostic Value on Growth Hormone Deficiency and Prognostic Value on the Response to Growth Hormone Therapy? seniha kiremitci yilmaz Received Received
  782-P2 EARLY PUBERTY; DIAGNOSIS, TREATMENT AND PROGNOSIS esra doger Received Received
  783-P2 BASAL LEVELS OF FSH AND LH CAN BE HELPFULL IN DIAGNOSIS OF PUBERTY PRECOCIOUS? Ulku Gul Received Received
  784-P2 Body Mass Index and Body Fat Composition are Both Related to Central Precocious Puberty in Chinese Girls Ke Huang Received Received
  785-P2 HYPERLEPTINEMIA IN OBESE AND NON-OBESE CHILDREN WITH EARLY PUBERTY KYUNG-MI JANG Received Received
  786-P2 Association between Congenital Hypopituitarism and Agenesis of the Internal Carotid Artery: a case report. Alessandra Cocca Received Received
  787-P2 Giant macroprolactinoma in a female adolescent - case report Ana Hreniuc Received Received
  788-P2 ADENOMAS PITUITARY IN CHILDREN soumeya fedala Received Received
  789-P2 A Patient With Multiple Endocrine Neoplasia Type 1 Presented With Precocious Puberty Nese Akcan Received Received
  790-P2 PRECOCIOUS PUBERTY IN A GIRL WITH PRADER WILLI SYNDROME (PWS) MARIA PAPAGIANNI Received Received
  791-P2 MENSTRUAL CHARACTERISTICS AND PROBLEMS IN 918 YEARS OLD TURKISH SCHOOL GIRLS Mustafa Kendirci Received Received
  792-P2 Haplo-insufficiency for LHX4 alone does not result in hypopituitarism. Evelien Gevers Received Received
  793-P2 A Nursing Perspective: Best practices for pubertal suppression for individuals with central precocious puberty and transgender Eileen Pyra Received Received
  794-P2 An unusual association between empty sella and central precocious puberty Stefano Stagi Received Received
  795-P2 CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT (CAKUT) IN CHILDREN BORN SMALL FOR GESTATIONAL AGE (SGA) - OUR EXPERIENCES Aleksandra Janchevska Received Received
  796-P2 Severe Juvenile Hypertrophy of the Breast with hypercalcaemia; mastectomy vs reduction surgery David McGregor Received Received
  797-P2 Report two cases of dopa-responsive dystonia. zhuannan Jiang Received Received
  799-P1 NPR2 gene mutations associated with acromesomelic dysplasia Maroteaux type are mostly unique to families Lidia Castro-Feijoo Received Received
  800-P1 Rare cases of ornithine transcarbamylase deficiency and variant Turner syndrome Yoo-Mi Kim Received Received
  801-P1 Prepubertal ultra-low-dose estrogen therapy is associated with better lipid profile than conventional estrogen replacement for pubertal induction in adolescent girls with Turner syndrome preliminary results. Malgorzata Wojcik Received Received
  802-P1 COGNITIVE EVALUATION IN SILVER RUSSELL CHILDREN GIUSEPPA PATTI Received Received
  803-P1 Body Surface Area Estimation In Girls With Turner Syndrome:Implications For Interpretation Of Aortic Sized Index Sze Choong Wong Received Received
  804-P1 Near-adult height in a large cohort of patients with Turner syndrome and Noonan syndrome treated with rhGH: Results from Pfizer International Growth Database (KIGS) Ferah Aydin Received Received
  805-P1 Percutaneous epiphysiodesis around the knee to reduce predicted excessive final height. Results of final height, complications and satisfaction in a large cohort of Dutch boys and girls. Wesley Goedegebuure Received Received
  806-P1 Metabolic Health and Long-term Safety of GH-Treatment in Silver-Russell Syndrome Carolina Smeets Received Received
  807-P1 Auxological features in patients with Juvenile Idiopathic Arthritis (JIA) treated with biologic therapy preliminary study data Stefano Stagi Received Received
  808-P1 Identification of 11p14.1-p15.3 Deletion Probably Associated with Short Stature, Macrocephaly and Delayed Closure of the Fontanelles SUMITO DATEKI Received Received
  809-P1 Early treatment with rhGH in patients with Prader-Willi syndrome results in improved height with no respiratory adverse effects. Kyriaki Alatzoglou Received Received
  810-P1 Phenotypic variability in a family with a new SHOX gene mutation Adalgisa Festa Received Received
  811-P1 Correlations between prepubertal and pubertal estrogen levels and final height out-come in growth hormone (GH) treated boys with Silver Russell syndrome (SRS) Kjersti Kvernebo-Sunnergren Received Received
  812-P1 Skeletal Disproportion In Girls With Turner Syndrome Sze Choong Wong Received Received
  813-P1 Reconsideration of mid-parental height calculation Serap Turan Received Received
  814-P1 Altered Thyroid function following Growth Hormone (GH) Initiation in children with Prader-Willi syndrome (PWS) Musthaffa Yassmin Received Received
  815-P1 6-year-old girl with mutation in DNMT3A a new overgrowth syndrome. Ann-Margrethe Rnholt Received Received
  816-P1 A case of patient with Rubinstein-Taybi Syndrome type 2 with complete deletion of EP300 gene and complex phenotype. Romana Marini Received Received
  817-P1 Silver-Russell syndrome with 11p15 epimutation: clinical analysis of adrenarche, central puberty and body mass index in a cohort of French children Ana Canton Received Received
  818-P1 Haploinsufficiency of short stature homeobox containing gene (SHOX): clinical signs and anthropometric measurements in children. Alice Monzani Received Received
  819-P1 Clinical and molecular characterization of a newly recognized overgrowth syndrome: interstitial 7q22.1-7q22.3 microdeletion Chong Kun Cheon Received Received
  820-P1 INTERNATIONAL COOPERATIVE GROWTH STUDY, NutropinAq European Registry (iNCGS): Countries specificities Nick Brown Received Received
  821-P1 CASE REPORT OF 48 XXYY SYNDROME ASSOCIATED TO FATHERS RADIOACTIVE CONTAMINATION DURING THE CESIUM ACCIDENT IN GOINIA - GOIÁS, BRAZIL. RENATA MACHADO PINTO Received Received
  822-P1 Neonatal haematological complication in Noonan syndrome future concerns about growth hormone therapy Laura Kasongo Received Received
  823-P1 Effects of a Stressful Environment (SE) on Height, BMI and Menarche Alina German Received Received
  824-P1 GROWTH HORMONE DEFICIENCY IN NOONAN SYNDROME: DOES IT INFLUENCE CLINICAL RESPONSE TO GH THERAPY? Maria Chiara Pellegrin Received Received
  825-P1 Screening of Birth Length and Parental Height Detects Infants With Poor Catch-Up Growth at Age 2 Years Colette Montgomery Sardar Received Received
  826-P1 Etiologic distribution and characteristics of patients with short stature in a Pediatric Endocrinology Clinic Saygin Abali Received Received
  827-P1 OSBPL5 methylation abnormalities may be pathogenic in Silver Russell syndrome through genomic methylation analysis DI WU Received Received
  828-P1 A study of Bone Health Index (BHI) in girls with Turners Syndrome Joanne Blair Received Received
  829-P1 Premature adrenarche in Silver-Russell syndrome: a longitudinal study Nawfel Ferrand Received Received
  830-P1 A RARE CASE OF DELETION IN 2q24.1: CLINICAL FEATURES AND RESPONSE TO GH HORMONE TREATMENT Maria Cristina Maggio Received Received
  832-P1 Effect of dietetic management on weight in children with Bardet-Biedl Syndrome Suma Uday Received Received
  834-P2 Auxological Features in Patients with Vernal Keratoconjunctivitis Stefano Stagi Received Received
  835-P2 Turner Syndrome: does GH treatment influence glucose homeostasis? Federico Baronio Received Received
  836-P2 Renal anomalies in children with Turner Syndrome: experience from a single-centre Laura Lucaccioni Received Received
  838-P2 A novel fibrillin-1 gene mutation leading to Marfan syndrome in Korean girl Hyo-Kyoung Nam Received Received
  839-P2 Evaluation of Referrals for Short Stature to a Regional Paediatric Centre David Yue Received Received
  840-P2 Testosterone Therapy Improves the first year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty(CDGP) GIRI Dinesh Received Received
  841-P2 Effects on Growth and Safety of Growth Hormone (GH) in Combination with the Gonadotrophin Releasing Hormone Agonist (GnRH) Leuprorelin in Pubertal Children with Idiopathic Short Stature (ISS) Hannah Williams Received Received
  842-P2 Linear Growth in Infants and Children with Atopic Dermatitis. Ashraf Soliman Received Received
  843-P2 The specific pubertal height gain is higher in boys as well as in children with lower BMISDS Anton Holmgren Received Received
  844-P2 Growth Screening in children aged three to five years seen in Community Paediatrics in Dreux District, France. Preliminary results. SIMON K. KAYEMBA-KAYS Received Received
  845-P2 THE 3M SYNDROME: A CAUSE OF PRE- AND POST-NATAL SEVERE GROWTH RETARDATION Firdevs Bas Received Received
  846-P2 Should we construct specific growth charts for ethnic subgroups? Pop Raluca-Monica Received Received
  847-P2 Late presenting girls with Turner Syndrome (TS) can achieve a normal final height. Sophia Sakka Received Received
  848-P2 GROWTH OF CHILDREN BORN PRETERM DURING THE FIRST 8 YEARS OF LIFE Adriane Cardoso-Demartini Received Received
  849-P2 Genetic variability in patients with Noonan syndrome in the Republic of Macedonia Mirjana Kocova Received Received
  850-P2 An unusual cause of short stature in a phenotypic male with Type I Diabetes Mellitus due to an unexpected deletion of the Y chromosome Dinesh Giri Received Received
  851-P2 AN UNUSUAL CASE OF GROWTH HORMONE REPLACEMENT THERAPY IN A CHILD WITH HEREDITARY MULTIPLE EXOSTOSES AND GROWTH HORMONE DEFICIENCY MARIA CHATZIPSALTI (XATZIPSALTI) Received Received
  852-P2 Assessment of the medical and psychological status of women with Turner-Syndrome in young adulthood Diana-Alexandra Ertl Received Received
  853-P2 A 3-year-old boy with growth hormone deficiency and clinical features of Ritscher-Schinzel syndrome Sonya Galcheva Received Received
  854-P2 Growth pattern, response to GH treatment and the effects of pubertal spurt on final height in patients affected by RASopathies Laura Mazzanti Received Received
  855-P2 The usefulness of magnetic resonance imaging of the heart and aortain the diagnostic work-up in girls with Turner syndrome Monika Obara-Moszynska Received Received
  856-P2 A RARE CAUSE OF SHORT STATURE: PATIENT WITH 3M SYNDROME REVEALED A NEW MUTATION IN OSBL1 GENE Meliksah Keskin Received Received
  857-P2 A case of familial Silver-Russell syndrome Julia Hoppmann Received Received
  858-P2 Central precocious puberty in a case of SOTOS syndrome Sharon Lim Received Received
  860-P2 Referral Pattern of Children with Short Stature to a Pediatric Endocrine Clinic in Kuwait Al-Abdulrazzaq Dalia Received Received
  861-P2 The Effect of Iron Intervention on the Anthropometric Parameters: Pilot Study among Egyptian Preschool Children with Iron Deficiency Anemia Amany Ibrahim Received Received
  862-P2 Dopamine Beta-Hydroxylase Deficiency Leading to Growth Hormone Deficiency Hakan Dneray Received Received
  863-P2 Quality of life in growth hormone treated children and adolescents with growth hormone deficiency and smallness for gestational age. jean de schepper Received Received
  865-P2 Postnatal Growth and Factors Modifying it in Very Low Birth Weight Preterms (PT) with Bronchopulmonary Dysplasia (BPD). Ashraf Soliman Received Received
  866-P2 Endocrine and metabolic parameters before onset of rGH treatment : potential predictive factors of GH response in children born SGA? Results from cohort of Nancy Emeline RENARD Received Received
  867-P2 Growth Hormone treatment in a child with Trisomy 21 and Turner Mosaicism Sharon Lim Received Received
  868-P2 Pubertal development and Final Height in some rare genetic diseases. LAURA MAZZANTI Received Received
  869-P2 Growth hormone deficiency in a patient with ring chromosome 18 Maria Korpal-Szczyrska Received Received
  870-P2 Children with Down syndrome show quantitative, phenotypical and functional differences of effector T-cells compared to immunocompetent controls Justine Schoch Received Received
  871-P2 CARDIOVASCULAR ANOMALIES IN TURNER SYNDROME soumeya fedala Received Received
  872-P2 Metamemory in Turner syndrome: a study comparing episodic and semantic memory Céline Souchay Received Received
  873-P2 A XO/XX girl with lack of morphological UTS-features, short stature and precocious puberty Birgit Vogel Received Received
  874-P2 Transverse Myelitis in Turner Syndrome Cristiane Kopacek Received Received
  875-P2 Tricho-Rhino-Phalangeal Syndrome Type I in a girl with Growth Hormone Deficiency Meltem Didem Cakir Received Received
  877-P2 Pituitary gigantism and central precocious puberty presenting with prognathism in a pediatric patient Carla Minutti Received Received
  878-P2 The monitoring of endocrine functions in children with rare genetic syndromes Natallia Akulevich Received Received
  880-P2 Late diagnosis of mixed gonadal dysgenesis - clinical and psychological implications Mirela Puiu Received Received
  881-P2 The structure of genetically determined types of short stature in Uzbekistan according to retrospective analysis Nilufar Ibragimova Received Received
  882-P2 EVALUATION OF GROWTH PATTERN IN PRADER-WILLI SYNDROME Sevinc Odabasi Gunes Received Received
  883-P2 Prader-Willi Syndromedifferent patients, different attitude Anamaria Bursuc Received Received
  884-P1 CLINICOPATHOLOGICAL CHARACTERISTICS OF PAPILLARY THYROID CANCER IN CHILDREN WITH EMPHASIS ON THE PUBERTAL STATUS AND ASSOCIATION WITH BRAFV600E MUTATION SUKRAN POYRAZOGLU Received Received
  885-P1 Elevation of serum fibroblast growth factor 21 in congenital hypothyroidism Shuichi Yatsuga Received Received
  886-P1 Evaluation of Epicardial Adipose Tissue Thickness in Children Detected Subclinical Hypothyroidism Ayca Torel Ergur Received Received
  887-P1 EEG alterations are common in Hashimotos Thyroiditis Claudia Boettcher Received Received
  888-P1 Semi-hot thyroid nodules associated with GNAS mutations in three adolescents ANNE-SPOHIE LAMBERT Received Received
  889-P1 Evaluation of Body Composition via Bioelectrical Impedance Analysis in Children with Subclinical Hypothyroidism and Effect of LT4 treatment;Follow-up Results Sevinc Odabasi Gunes Received Received
  890-P1 The molecular causes of congenital hypothyroidism: The Scottish experience mariam kourime Received Received
  891-P1 Newborn Screening Program for Congenital Hypothyroidism: eighteen years of experience in Buenos Aires Province, Argentina. Verónica González Received Received
  892-P1 Transient TSH elevation in infants referred on newborn screening features, prevalence and trends Yasmine Ouarezki Received Received
  893-P1 Resolution of hepatic hemangiomas and consumptive hypothyroidism in an infant treated with propranolol and levothyroxine Victoria Campbell Received Received
  894-P1 Comprehensive analysis of seven Toll-like receptor genes including 15 single-nucleotide polymorphisms with autoimmune thyroid disease in Korean children. cho wonkyoung Received Received
  895-P1 Thyroid cancer is the most frequent secondary solid tumour following allogeneic stem cell transplantation in childhood a single centre experience Marta Snajderova Received Received
  896-P1 Iodide transport defect: Identification of a novel mutation in the carboxy-terminus of the sodium/iodide symporter in a pediatric patient with congenital hypothyroidism Juan Nicola Received Received
  897-P1 Congenital Hypothyroidism: The Use of a TSH Cut-off Limit of 6mU/L and the ESPE Criteria for LT4 treatment Leads to the Diagnosis of Mild but mostly Permanent Forms of Hypothyroidism. Voutetakis Antonis Received Received
  898-P1 Do different initial doses of L-T4 within the range of 10-15 mcg/kg/day influence neurodevelopment during the first two years of life in children with congenital hypothyroidism? Andrea Esposito Received Received
  899-P1 Clinical And Histopathologic Features And Follow-Up Of Paediatric Patients With Papillary Thyroid Cancer: A 10 Years Experience. ROBERTO ZUART Received Received
  900-P1 Meta-analysis of children with Multiple Endocrine Neoplasia (MEN) Type 2A from 1995-2014: Impact of RET mutation screening on age at thyroidectomy and frequency of metastatic disease Marie-Anne Burckhardt Received Received
  901-P1 Screening of congenital hypothyroidism in low birth weight and very low birth weight neonates: A systematic review Mahin Hashemipour Received Received
  902-P1 Identification of zinc transporter ZnT8 in thyroid tissues from children and adolescents with thyroid nodular hyperplasia Artur Bossowski Received Received
  903-P1 HABP2 as genetic susceptibility factor for Familial Differentiated Thyroid Carcinoma. Rajdee de Randamie Received Received
  904-P1 Cardiac size and function in children with subclinical hypothyroidism Sara Alfano Received Received
  905-P1 Association of CTLA4, PADI4 and FTO polymorphisms with autoimmune thyroid diseases in male children. Aleskandra Goralczyk Received Received
  906-P1 Thyroid cancers in Korean pediatric populations with thyroid nodules SO HYUN PARK Received Received
  907-P1 Dysregulation of the immune system in children with Graves disease the role of NK and NKT-like cells Maria Klatka Received Received
  908-P1 Thyroid function anomalies in children with Down syndrome: early TSH alteration can predict future hypothyroidism development? Giorgio Ottaviano Received Received
  909-P1 Identification of a cryptic de novo deletion in NKX2.1 in the Brain-Lung-Thyroid Syndrome using genome-wide arrays BEATRIZ VILLAFUERTE Received Received
  911-P1 Hyperthyroidism after Bone Marrow Transplantation: A Report of Two Cases Hiroyuki Ishiguro Received Received
  912-P1 A case of young girl with high risk RET mutation successfully diagnosed as medullary thyroid carcinoma in very early stage. Yuki Abe Received Received
  913-P1 Nerve Conduction Studies in Children with Subclinical Hypothyroidism Gonul Catli Received Received
  915-P1 Macro TSH- a Rare Cause of High Levels of TSH Selin Elmaogullari Received Received
  916-P1 Papillary thyroid carcinoma in a mother and child after manifestation of Graves disease Erwin Lankes Received Received
  917-P1 Hypercholesterolemia in two siblings with THRB mutation Urh Groselj Received Received
  918-P1 Thyroid Autoimmunity and Vitamin D Status in Euthyroid Girls with Hashimotos Thyroiditis Pinar Isguven Received Received
  919-P1 Etiology and severity of congenital hypothyroid children detected through neonatal screening: a cut-off based analysis Ana Vieites Received Received
  920-P1 Lowering of the TSH cut-off limit substantially alters universally accepted key features of Congenital Hypothyroidism. Reconsideration of the use of FT4 levels for diagnosis and treatment. Voutetakis Antonis Received Received
  921-P1 Differentiated thyroid cancer: onset and outcome in a pediatric population with and without risk factors Federico Baronio Received Received
  922-P1 Evaluation of the usefulness of serum cytokines IL-1 and sFasL measurements in the diagnosis of autoimmune hypothyroidism and hyperthyroidism in children Marcin Mikos Received Received
  923-P1 Small thyroid volume on ultrasound in infants with transient TSH elevation following referral by newborn screening Chourouk Mansour Received Received
  924-P1 In children with autoimmune thyroid diseases the association with Down syndrome can modify the clustering of extra-thyroidal autoimmune disorders Malgorzata Wasniewska Received Received
  925-P1 L-selenomethionine supplementation in children and adolescents with autoimmune thyroiditis: preliminary results of a randomized double-blinded placebo-controlled clinical trial Ioannis Kyrgios Received Received
  926-P1 Minimally invasive video-assisted thyroid surgery (MIVAT) in children: a single center ten-years experience graziamaria ubertini Received Received
  927-P1 PREVALENCE OF CONGENITAL HYPOTHYROIDISM AND THYROID FUNCTION FOLLOW-UP OF CHILDREN WITH TSH CUTOFF BETWEEN 5 AND 10 mU/L IN NEONATAL SCREENING Lemos-Marini Sofia Helena V Received Received
  928-P1 PRELIMINARY RESULTS: BODY COMPOSITION OF ADOLESCENT PATIENTS WITH CONGENITAL HYPOTHYROIDISM AND CORRELATION WITH LABORATORY PARAMETERS Artemis Doulgeraki Received Received
  929-P1 Neonatal thyrotoxicosis and craniosynostosis associated with maternal Graves disease and high dose maternal thyroxine therapy for papillary carcinoma Sumudu Seneviratne Received Received
  930-P1 Seasonality of month of birth in children and adolescents with Hashimoto thyroiditis Ioannis Kyrgios Received Received
  931-P1 Radioiodine therapy for Graves disease the experience of a Portuguese single centre Nuno Vicente Received Received
  932-P2 MULTINODULAR GOITER AND DIFFERENTIATED THYROID CANCER IN PEDIATRICS Patricia Papendieck Received Received
  933-P2 Clinical case of acute liver injury in pediatric patient with autoimmune hyperthyroidism MARIA CRISTINA VIGONE Received Received
  934-P2 Thyroid function in children affected by Congenital Hypothyroidism (CH) with eutopic thyroid after discontinuation of treatment with Levothyroxine ROBERTO GASTALDI Received Received
  935-P2 HYPERTHYROIDISM IN AN INFANT OF A MOTHER WITH AUTOIMMUNE HYPOTHYROIDISM WITH POSITIVE TSH RECEPTOR ANTIBODIES margaret zacharin Received Received
  936-P2 THYROID CANCER PRESENTATION IN CHILDREN IS DIFFERENT THAN IN YOUNG ADULTS Malgorzata Wasniewska Received Received
  937-P2 Starting treatment in congenital hypothyroidism with normal FT4 levels and thyroid gland in situ detected at neonatal screening Laura Paone Received Received
  938-P2 Distal monosomy 10q presented as congenital hypothyroidism Elena Emanuela Braha Received Received
  939-P2 Five-year prospective evaluation of thyroid function test evolution in children with Hashimotos thyroiditis presenting with either euthyroidism or subclinical hypothyroidism Malgorzata Wasniewska Received Received
  940-P2 An unusual case of impaired renal function and thrombocytopenia Luminita Nicoleta Cima Received Received
  941-P2 Celiac Disease in Children and Adolescents with Hashimoto Thyroiditis Hale Tuhan Received Received
  942-P2 Euthyroid Hashimoto thyroiditis in children : evolution over time FENELI KARACHALIOU Received Received
  943-P2 Thyrotoxic Periodic Paralysis, an under-recognized condition Carolina Di Blasi Received Received
  944-P2 Age at diagnosis and mental development in children with congenital hypothyroidism in the absence of newborn screening programme. Yasmine Ouarezki Received Received
  946-P2 The clinical predictive factors for differentiation transient congenital hypothroidism from congenital hypothyroidsm patients Se Young Kim Received Received
  947-P2 Delayed Diagnosis of a TSH-adenoma Due to Coexisting Autoimmune Thyroid Disease David Crudo Received Received
  948-P2 Kocher-Debre-Semelaigne syndrome: hypothyroidism with muscle pseudohypertrophy. Elena Bogova Received Received
  949-P2 Thyroid function in obese children and its correlations with chosen atherogenic risk factors Beata Pyrzak Received Received
  950-P2 The evolution of thyroid function after Hashimotos thyroiditis presentation is different in initially euthyroid girls with or without Turner syndrome Malgorzata Wasniewska Received Received
  951-P2 Hashimotos Thyroiditis in childhood: an 8 year experience SOTIRIA GIANNOPOULOU Received Received
  952-P2 Congenital Malformations, Dysmorphic Syndromes and Neurodevelopmental Problems in Children with Congenital Hypothyroidism Voutetakis Antonis Received Received
  953-P2 Clinical value of thyroid-stimulating immunoglobulin in paediatric autoimmune thyroid diseases Karolina Stozek Received Received
  954-P2 Hearing, language and communication abilities in children with congenital hypothyroidism Hannah Cooper Received Received
  955-P2 Lack of catch up growth in young children with severe Hashimoto thyroiditis Audrey VINCENT Received Received
  956-P2 Perinatal factors associated with neonatal thyroid stimulating hormone in normal newborns Seong Yong Lee Received Received
  958-P2 Beta thallassemia : the relation between ferritin and hypothyroisdism and the suppressing effect of ferritin on autoimmune disorders (a hypothesis) setila dalili Received Received
  959-P2 Thyroid hormones and risk factors in obese and overweight children SOTIRIA GIANNOPOULOU Received Received
  960-P2 FNA: a gold standard in the diagnosis of thyroid nodules in children after chemotherapy SOFIA LEKA Received Received
  961-P2 Profound growth failure in peripubertal adolescents presenting with severe acquired autoimmune hypothyroidism a case series Swathi Upadrasta Received Received
  962-P2 TWO PATIENTS WITH RESISTANCE TO THYROID HORMONES ESRA DENIZ PAPATYA CAKIR Received Received
  963-P2 The influence of etiology and treatment factors on intellectual outcome in congenital hypothyroidism Jong Seo Yoon Received Received
  964-P2 An unusual complication of Graves disease. Akintayo Adesokan Received Received
  965-P2 An unusual form of precocious puberty: Van Wyk and Grumbach syndrome AHMET ANIK Received Received
  966-P2 Clinical Features of Newborn with Congenital Hypothyroidism Diagnosed by Neonatal Screening: Single Center Experience AYLA GUVEN Received Received
  967-P2 Postoperative complications of thyroidectomy in children with nodular goiter Olga Rogova Received Received
  969-P2 An unusual presentation of Hashimoto thyroiditis (HT) and precocious puberty: The VAN WYK-GRUMBACH Syndrome SOFIA LEKA Received Received
  970-P2 Rare Case of Severe Hyperthyroidism due to Graves Disease in a Toddler Parissa Salemi Received Received
  971-P2 Youngest Known Case of Autoimmune Thyroiditis Causing Hyperthyroidism in a Downs Syndrome Toddler Parissa Salemi Received Received
  972-P2 Thyroid hormones in obese children SOTIRIA GIANNOPOULOU Received Received
  973-P2 A case of neonatal Graves in a premature infant with negative thyrotropin receptor stimulating antibodies Carla Minutti Received Received
  974-P2 Severe growth retardation and hypothyroidism due to Hashimotos thyroidits Marina Krstevska-Konstantinova Received Received
  975-P2 Beta thallassemia : the relation between ferritin and hypothyroisdism and the suppressing effect of ferritin on autoimmune disorders (a hypothesis) setila dalili Received Received
  976-P2 Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroidism Gonul Buyukyilmaz Received Received
  977-P2 Very early onset of autoimmune thyroiditis in a toddler with multi-organ involvement Giuseppina Rosaria Umano Received Received
  978-P2 The case of the thyroid gland dystopia in the root of the tongue Svitlana Chumak Received Received
  979-P2 A case report:Conversion of autoimmune hypothyroidism to hyperthyroidism in A child with Downs syndrome. abdullah alshahrany Received Received
  980-P2 Transient congenital hypothyroidism: About 6 cases soumeya fedala Received Received
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EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

55th Annual ESPE Meeting 2016

 

10-12 September 2016 Paris
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                   DOI: 10.3252/pso.eu.55ESPE.2016 
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