PosterSessionOnline

EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

55th Annual ESPE Meeting 2016

10-12 September 2016 Paris

N. Poster

Poster title

Applicant name

Status


1-5-RFC	A novel animal model to study 21-hydroxylase deficiency in vivo	Andreas Zaucker	Received

1-7-RFC	Recovery of adrenal function in children with asthma assessed by Low Dose Short Synacthen Test (LDSST)	Arundoss Gangadharan	Received

1-4-RFC	Mutations of ABCD1 in 16 Vietnamese Patients with X-linked Adrenoleukodystrophy	Dung Vu Chi	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

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

1-6-RFC	Pediatric patients with congenital adrenal hyperplasia have unfavorable changes in their cardiovascular risk profile	Christiaan Mooij	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

1-3-RFC	Impaired cardiac function in a mouse model of Generalized Glucocorticoid Resistance	Penio Kassari	Received

1-2-RFC	Glucocorticoid deficiency due to disruption of mitochondrial steroidogenesis leads to dysregulation of antioxidant pathways and nucleotide biosynthesis	Meltem Weger	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

2-4-RFC	Results of orthopaedic surgery in children with X-linked hypophosphatemic rickets (XLHR)	AGNES LINGLART	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

2-LBP	Sexual Outcomes in Brazilian Patients with 46,XY DSD Patients	Rafael Loch Batista	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

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

2-8-RFC	Final heights and BMI in patients affected with different types of pseudohypoparathyroidism	hanna hanna	Received

2-P1	Mast cells and steroidogenesis in the human fetal adrenal	Alexandre Naccache	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

2-7-RFC	Effect of paternal loss-of-function mutations of GNAS on growth during the childhood: a role for XL.	Lea Tran	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

3-3-RFC	Unraveling the Link Between Optic Nerve Hypoplasia and Pituitary Hormone Dysfunction	Naseem Alyahyawi	Received

3-7-RFC	Pituitary structural abnormalities in idiopathic isolated growth hormone deficiency	Luis Cardoso	Received

3-6-RFC	Priority target conditions of growth-monitoring in children: toward consensus	Pauline SCHERDEL	Received

3-2-RFC	Subfertility After Chemotherapy in PNET tumours: 34 Year Experience From a Single Centre (1980-2013)	Joana Serra-Caetano	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

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

3-8-RFC	Anthropometric and endocrine features in children and adolescents with Type 1 Narcolepsy.	Antonio Balsamo	Received

3-P1	Gender-specific differences in hypothalamus-pituitary-adrenal axis activity in children.A meta-analysis	Bibian van der Voorn	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

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

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

4-5-RFC	Steroid Metabolomic Signature of Liver Disease in Childhood Obesity	Aneta Gawlik	Received

4-LBP	Sirolimus precipitating Diabetes in a patient with Congenital Hyperinsulinism due to autosomal dominant ABCC8 mutation	ANTONIA DASTAMANI	Received

4-6-RFC	Adipose tissue - a source of hyperandrogenism in obese females?	Isabel Wagner	Received

4-2-RFC	Adipocytokines delay pubertal maturation of human Sertoli cells	Isabel Wagner	Received

4-1-RFC	Immune-fat-bone axis in obese children: the role of LIGHT	Brunetti Giacomina	Received

4-P1	Prepubertal children born large for gestational age have lower serum DHEAS concentrations than those with lower birth weight	Henrikki Nordman	Received

4-7-RFC	Prevalence and characterization of retinal alterations in a cohort of overweight and obese children	Stefania Pedicelli	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

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

5-6-RFC	Clinical management of the Mitchell-Riley syndrome due to RFX6 gene mutations: aggressive support results in improved outcome	Poidvin Amélie	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

5-4-RFC	TRANSIENT NEONATAL DIABETES IN ADULTHOOD: METABOLIC OUTCOMES	kanetee busiah	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

5-5-RFC	The efficacy of insulin degludec in children and adolescents with type 1 diabetes.	Barbara Predieri	Received

5-3-RFC	Sexual lifestyle among young adults with type 1 diabetes	Orit Pinhas-Hamiel	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

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

6-2-RFC	RAB3IP and DGCR8 as a potentially pathogenic novel candidate gene involving in growth disorders	Thais Homma	Received

6-P1	Novel CYP11A1 mutations in 15 patients (13 families) with variable clinical presentations	Claire Goursaud	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

6-4-RFC	Growth hormone (GH) treatment in skeletal dysplasias Short-term results in prepubertal children reported in KIGS	Ferah Aydin	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

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

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

7-2-RFC	Reference values for external genitalia size and steroid hormone levels in female neonates.	Sarah Castets	Received

7-4-RFC	A Mutation in WT1 (Wilms tumor suppressor 1) associated with 46,XX TDSD	Caroline Eozenou	Received

7-LBP	Loss of functional Osteoprotegerin: more than a skeletal Problem	Corinna Grasemann	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

7-3-RFC	Harmonisation of Serum Dihydrotestosterone Analysis: Establishment of an External Quality Assurance Program	Michaela Hartmann	Received

7-5-RFC	FERTILITY PRESERVATION IN AN ADOLESCENT BOY: INDUCING PUBERTY AND SPERMATOGENESIS PRIOR TO BONE MARROW TRANSPLANTATION	margaret zacharin	Received

7-6-RFC	FERTILITY PRESERVATION FOR CHILDREN AND ADOLESCENTS A REPORT OF CURRENT PRACTICE	Cindy Ho	Received

7-P1	Transient Generalized Glucocorticoid Hypersensitivity Syndrome	Eleni Magdalini Kyritsi	Received

7-7-RFC	Clinical Decision-Making in Disorders of Sex Development (DSD): Physician Recommendations Pre- and Post-Consensus Statement	David Sandberg	Received

7-8-RFC	Premature adrenarche in girls at pubertal onset is associated with high androgens, but lower AMH concentrations	veronica mericq	Received

8-LBP	Impact of weight loss after bariatric surgery on gonadic function in severely obese female adolescents	Iva Gueorguieva	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

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

8-5-RFC	Optimal Sampling of IGF-1 During Weekly Administration of a Long Acting Human Growth Hormone (MOD 4023)	Gili Hart	Received

8-3-RFC	Batch-to-Batch Consistency of a Highly O-Glycosylated Long-Acting Human Growth Hormone (MOD-4023)	Gili Hart	Received

8-1-RFC	Somavaratan (VRS-317) Treatment of Children with Growth Hormone Deficiency (GHD): Results at 2 Years (NCT02068521)	Ingrid Koo	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

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

8-P1	The Effect of Obesity on the Stress Response: The Paradigm of Surgical Stress	Voutetakis Antonis	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

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

9-3-RFC	Molecular analysis of a large cohort of MODY patients by Next Generation Sequencing.	Stefano Stagi	Received

9-4-RFC	Prevalence of monogenic diabetes in the Lithuanian pediatric and young adult population	Valerie Schwitzgebel	Received

9-5-RFC	NON-MODY MONOGENIC DIABETES: A VERY HETEROGENOUS AND PROBLEMATIC GROUP OF DIABETES	Zeynep SIKLAR	Received

9-P1	Long-term anthropometric outcome of girls with non-classical congenital adrenal hyperplasia diagnosed in childhood	Rachel Bello	Received

9-2-RFC	Missense mutation of GLIS3 gene resulting inneonatal diabetes and congenital hypothyroidism	nadia alghazir	Received

9-LBP	Osteoprotegerin and insulin resistance in childhood obesity: a new interplay?	Eleni P Kotanidou	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

9-7-RFC	Chronotype and Type 2 Diabetes Risk in Preadolescents	Magdalena Dumin	Received

10-8-RFC	GESTATIONAL DIABETES IS ASSOCIATED WITH CHANGES IN PLACENTAL MICROBIOTA AND MICROBIOME	Judit Bassols	Received

10-2-RFC	DYSREGULATION OF PLACENTAL MIRNA IN MATERNAL OBESITY IS ASSOCIATED WITH PRE-AND POST-NATAL GROWTH	Judit Bassols	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

10-4-RFC	Pharmacokinetics of Intravenous Glucagon in Children with Hyperinsulinaemic Hypoglycaemia	PRATIK SHAH	Received

10-5-RFC	Phenotype, Genotype and Short term Outcome in Congenital Hyperinsulinism(CHI)	MUDITA DHINGRA	Received

10-LBP	Molecular analysis of AR, SRD5A2, NR5A1 and HSD17B3 genes in a Brazilian 46,XY DSD cohort.	Reginaldo Petroli	Received

10-P1	Current Dilution Methods cause Large Variations and Inaccuracies when making up 1mcg Synacthen Dose.	Alexandra Cross	Received

10-6-RFC	Increased Islet Cell Neogenesis and Endocrine Cell Differentiation in Congenital Hyperinsulinism in Infancy	Mark Dunne	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

11-6-RFC	Falsely TSH and free thyroid hormone measurements in pediatric patients treated with high dose of biotin	Moran Gal	Received

11-3-RFC	Germline and somatic DICER1 mutations in familial Papillary Thyroid Carcinoma and Multinodular Goiter.	César Lumbreras	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

11-1-RFC	Central hypothyroidism and biallelic defect near the D/ERY motif of the TRHR gene	Marta Garcia	Received

11-7-RFC	Secondary thyroid cancer among childhood cancer survivors. A single institution experience.	Monica Muraca	Received

11-4-RFC	Thyroid function in monozygotic twins with intra-twin birth-weight-differences	Sandra Schulte	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

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

12-4-RFC	Molecular screening of MKRN3, DLK1 and KCNK9 genes in central precocious puberty	Anna Grandone	Received

12-LBP	An analysis of symptoms and signs of adrenal insufficiency in children with CAH admitted to hospital in Australia.	Georgina Chrisp	Received

12-6-RFC	Serum antimllerian hormone and inhibin B as potential markers for progressive central precocious puberty in girls	Ting Chen	Received

12-8-RFC	Circulating MKRN3 levels decline during puberty in healthy boys	Alexander Busch	Received

12-5-RFC	A novel MKRN3 nonsense mutation causing familial central precocious puberty	Athanasios Christoforidis	Received

12-P1	Testicular adrenal rest tumours in 50 boys, adolescents and adult male with congenital adrenal hyperplasia	Miroslav Dumic	Received

12-2-RFC	A novel mutation of KISS1R causing a normosmic isolated hypogonadotropic hypogonadism	Keisuke Yoshii	Received

12-7-RFC	Prevalence of organic lesions in males with central precocious puberty.	Stefania Pedicelli	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

13-LBP	HYPERPROLACTINEMIA IN CHILDREN AND ADOLESCENTS: A REVIEW OF PATIENTS PRESENTING TO A TERTIARY CENTER IN AUSTRALIA.	Komal Vora	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

13-2-RFC	The use of proteomics in the assessment of health status of offspring born after intracytoplasmic sperm injection (ICSI)	Ioanna Kosteria	Received

13-7-RFC	Early-onset obesity and hyperphagia associated with defects in the GNAS gene	Marta Garcia	Received

13-3-RFC	Effects of eating rate on satiety hormones, meal enjoyment and memory for recent eating: An fMRI study	Katherine Hawton	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

13-8-RFC	Measuring subcutaneous adipose tissue using ultrasound in children	Adela Chirita-Emandi	Received

14-P1	A unique case of dual opposing pathologies	Irene Fernandez Viseras	Received

14-4-RFC	Genetic diagnosis of congenital growth hormone deficiency by massive parallel sequencing using a target gene panel	MARILENA NAKAGUMA	Received

14-6-RFC	Effects of size at birth, childhood growth patterns and growth hormone treatment on telomere length	Carolina Smeets	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

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

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

14-7-RFC	GH influences plasma fasting adropin concentration in patients with Turner syndrome	Beata Wikiera	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

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

15-6-RFC	Safety of GH in Paediatrics: The GeNeSIS Prospective Observational Study Experience Between 1999 and 2015 (NCT01088412)	Chris Child	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

15-2-RFC	NR0B1 Frameshift Mutation in a Boy with Precocious Puberty and Normal Adrenal Function	Hirohito Shima	Received

15-8-RFC	Replacement of male mini-puberty	DIMITRIOS T. PAPADIMITRIOU	Received

16-P1	Cortisol response to ACTH stimulation test in non-classical congenital adrenal hyperplasia (NCCAH)	FENELI KARACHALIOU	Received

17-P1	Altered stress system activity in children with ADHD	Eleni Angeli	Received

18-P1	Adult individuals with classic congenital adrenal hyperplasia exhibit deficits in utive functions	Leif Karlsson	Received

19-P1	Heterozygous mutations in CYP11A1 gene can cause life-threatening salt wasting and failure to thrive	DIMITRIOS T. PAPADIMITRIOU	Received

20-P1	Antiviral HIV treatment - a new cause of transient neonatal adrenal insufficiency	Tanja Haamberg	Received

21-P1	Increased salivary and hair cortisol and decreased salivary alpha-amylase concentrations in obese prepubertal girls	Chrysanthe Papafotiou	Received

22-P1	An Assessment Of The Hypothalamic-Pituitary-Adrenal Axis In Children With Prader-Willi Syndrome	Andreas Kyriakou	Received

23-P1	The Urinary Steroidome of Children with Classic 21-Hydroxylase Deficiency Treated with Hydrocortisone	Clemens Kamrath	Received

24-P1	Adrenal insufficiency in ROHHADNETsyndrome (Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation, Autonomic Dysregulation and Neural Tumor)	Ramona Tallone	Received

25-P1	The psychosocial impact of Adrenal Insufficiency (AI) and Congenital Adrenal Hyperplasia (CAH) on children and their parents	Amy Simpson	Received

26-P1	Sex-specific differences in hypothalamus-pituitary-adrenal axis activity in newborns with very low birth weight	Bibian van der Voorn	Received

27-P1	Beckwith-Wiedemann Syndrome and Bilateral Phaeochromocytoma: a Diagnostic Challenge	Emily Cottrell	Received

28-P1	Combined glucocorticoid and mineralocorticoid deficiency related to a new NNT mutation : a case report.	Emilie Doye	Received

29-P1	Testicular adrenal rest tumours in patient with X-linked adrenoleukodystrophy	Igor Chugunov	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

32-P1	Molecular Confirmatory Test Improves the Accuracy of Congenital Adrenal Hyperplasia Diagnosis in Newborn Screening Program	Mirela Miranda	Received

33-P1	USEFULNESS OF CORTICOTROPIN TEST IN CHILDREN AND ADOLESCENTS WITH CLINICAL HYPERANDROGENISM	FENELI KARACHALIOU	Received

34-P1	Primary Adrenal Insufficiency in children: results from a large nationwide cohort	Martina Rezzuto	Received

35-P1	Follow-up of growth and puberty in children with premature adrenarche	Jani Liimatta	Received

36-P1	Early onset hypertension with primary hyperaldosteronism through mutation in the calcium channel CACNA1H - case report.	Corina Chirita	Received

37-P1	DNA Methylation Signatures Associated With Prenatal Dexamethasone Treatment	Leif Karlsson	Received

38-P1	Twenty Years Experience in Congenital Adrenal Hyperplasia: Clinical, Hormonal and Molecular Characteristics in a Large Cohort	Mirela de Miranda	Received

39-P1	Chronic adrenal insufficiency due to a mutation of Nicotinamide Nucleotide Transhydrogenase 1 (NNT1) : case report	Jacques WEILL	Received

40-P1	Cognitive Functions in Congenital Adrenal Hyperplasia	nermine amr	Received

41-P1	RET AND TP53 CONCOMITANT MUTATIONS: A CHALLENGING APPROACH TO A UNIQUE ASSOCIATION OF HIGH TUMOR PREDISPOSING CONDITIONS	matilde calanchini	Received

42-P1	Acute lysis of a giant pediatric adrenal cortical carcinoma following one dose of opDDD	Emmanuelle Motte	Received

43-P1	Severe Hypertension in a Girl: Cushing Syndrome or Apparent Mineralocorticoid Excess Syndrome? Utility of Molecular Study	Cristian Seiltgens	Received

44-P1	An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome	Glay Karagzel	Received

45-P1	Polymorphisms analyze in CYP21A2 gene associated with congenital adrenal hyperplasia (CAH)	Cristiane Kopacek	Received

46-P1	The effect of intrauterine stress on leukocyte telomere length in newborns	Penio Kassari	Received

47-P1	Predictive Factors for Premature Pubarche in a Large Cohort of Italian Children	Rossella Gaudino	Received

48-P1	Cardiac function in pediatric patients with congenital adrenal hyperplasia	Christiaan Mooij	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

50-P2	Ovarian cysts in a 46,XX patient with congenital lipoid adrenal hyperplasia and with spontaneous puberty	Irina Kopylova	Received

51-P2	Bone health index in children and adolescents with congenital adrenal hyperplasia	Hussain Alsaffar	Received

52-P2	Occasional detection of an adrenal incidentaloma in a female adolescent evaluated for cardiac arrhythmias.	Eleni P Kotanidou	Received

53-P2	Final height in congenital adrenal hyperplasia: a retrospective study	Martins Mariana	Received

54-P2	Hyperandrogenism in a 12-year old girl with a congenital porto-systemic shunt and congenital hepatic fibrosis	Mikolaj Danko	Received

55-P2	THE TREATMENT OF A FUNCTIONAL ADRENOCORTICAL CANCER WITH MITOTANE	Selim Kurtoglu	Received

58-P2	Isthmic spondylolisthesis in a pre-pubertal boy with congenital adrenal hyperplasia during aromatase inhibitor treatment.	Nadya Katherine Jaimes Fajardo	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

60-P2	A Case of Cushings Syndrome due to Adrenocortical Adenoma with Pubarche and Obesity	fatih gurbuz	Received

61-P2	Severe neonatal Cushing syndrome with multi-organ McCune Albright manifestations	ANNE-SPOHIE LAMBERT	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

63-P2	The evolution of bone age in girls with premature adrenarche (PA)	Anastasios Papadimitriou	Received

64-P2	Cushing syndrome due to adrenal adenoma in an adolescent patient and successful treatment with laparoscopic surgery	Bulent Hacihamdioglu	Received

65-P2	A novel mutation of DAX-1 (NR0B1) in a boy with X-linked adrenal hypoplasia congenita	Karine Gerster	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

67-P2	Successful medical management of severe neonatal Cushing syndrome with metyrapone, guided by mass spectrometry monitoring	Poidvin Amélie	Received

68-P2	FAMILY CHARACTER ISOLATED PHEOCHROMOCYTOMA BY MUTATION IN VHL GEN	FREIJO CONCEPCION	Received

69-P2	Exaggerated adrenarche and exogenous obesity: a diagnostic challenge	Beatriz Semer	Received

70-P2	Vitamin D insufficiency is related to premature adrenarche	onur akin	Received

71-P2	A case of 17 years-old boy with relapsing Cushing disease presenting vertebral compression fracture	Yoo-Mi Kim	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

73-P2	Patients with Congenital Adrenal Hyperplasia have significantly higher healthcare utilisation than the general paediatric population	John Porter	Received

74-P2	CHOLESTASIS AND HYPERCALCEMIA SECONDARY TO PANHYPOPITUITARISM IN A NEWBORN	Fatma Dursun	Received

75-P2	CLINICAL MANAGEMENT IN SECONDARY PSEUDOHYPOALDOSTERONISM: A CASE SERIES	Ahmet Ozdemir	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

77-P2	Management dilemmas in a genetically female child with congenital adrenal hyperplasia raised as a male	Sumudu Seneviratne	Received

78-P2	Primary Pigmented Nodular Adrenocortical Disease (PPNAD) justifying a pediatric case of ACTH-independent Cushing Syndrome (CS)	Cristiane Kopacek	Received

79-P2	Three Chinese Patients from Two Kindreds with Aldosterone Synthase Deficiency: Clinical Characteristic with Mutation Analysis Report	MELATI WIJAYA	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

82-P2	A novel mutation of HSD3beta2 presenting as hypospadias with salt-wasting in a male infant	Charles Buchanan	Received

83-P2	Testicular adrenal rest tumors in two young patients with congenital adrenal hyperplasia	Alina Daniela Belceanu	Received

84-P2	Hyperreninemic Hypoaldosteronism: clinical and genetic features in pediatric patients	Stefano Stagi	Received

86-P2	Congenital adrenal hyperplasia revealed by adrenal nodules	soumeya fedala	Received

87-P2	Urosepsis or Pseudohypoaldosteronism in a Neonate?	Noah Gruber	Received

88-P2	A Case Report of Adrenocortical Adenoma in a Young Girl	Huyen Tran	Received

90-P2	A Genetic Diagnosis Of Familial Glucocorticoid Deficiency Resulting In Cessation Of Long Term Mineralocorticoid Treatment In Three Siblings.	Emily Cottrell	Received

91-P2	Corticosteroid-induced adrenal insufficiency in a child with T cell lymphoblastic lymphoma: A case report	SangHyun Lee	Received

92-P2	Dilated Cardiomyopathy- A rare endocrine association with Congenital Adrenal Hyperplasia due to 11 beta hydroxylase deficiency.	Prashant Patil	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

94-P2	11- hydroxylase deficiency due to a novel compound heterozygous mutation and literature review	Wei Wu	Received

97-P2	Congenital adrenal hyperplasia Subtle presentations with critical electrolyte imbalances and cardiac arrhythmias.	Abirami Namasivayam	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

99-P1	Automated Greulich-Pyle bone age determinations in children with chronic endocrine diseases	Daniela Klose	Received

100-P1	Cord 25-hydroxy-vitamin D is not associated with cranial anthropometrics in infants.	Sissil Egge	Received

101-P1	Effect of bisphosphonates on bone fragility due to chronic liver disease in ten children	Alessia Usardi	Received

102-P1	Radiologically Confirmed Fractures In A Scottish Nationwide Cohort Of Boys With Duchenne Muscular Dystrophy	Shuko Joseph	Received

103-P1	Monostotic Fibrous Dysplasia is a single disorder caused by somatic mosaic activating mutations in GNAS	Hironori Shibata	Received

104-P1	Clinically significant fracture incidence in Czech children: a population-based study.	Ondrej Soucek	Received

105-P1	Effects of Selective GPER-1 Agonist G1 on Bone Growth	Maryam Iravani	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

107-P1	Bone mineral status in children and adolescents with Klinefelter Syndrome	Stefano Stagi	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

109-P1	Nonsense mutation in SPARC gene causing autosomal recessive ostegenesis imperfecta	SAYGIN ABALI	Received

110-P1	Increase in sclerostin after rapid weight loss in children.	Niels Birkebaek	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

112-P1	Bone Health and Body Composition in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting	Mahjouba Ahmid	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

114-P1	Extension of automated bone age determination to the end of puberty	David Martin	Received

115-P1	A European survey to identify new roads for care, training and research around rare metabolic bone diseases	Isabelle FERNANDEZ	Received

116-P1	Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients	Sarah Bakhamis	Received

117-P1	No severe hypercalcemia during a 12-month high-dose vitamin D intervention in infants	Saara Valkama	Received

118-P1	Management of tracheobronchomalacia during asfotase alfa treatment in infants with perinatal-onset hypophosphatasia: a case series	Raja Padidela	Received

119-P1	Novel p.Asn628Ser heterozygous mutation in FGFR1 is associated with Hartsfield syndrome and tumoral calcinosis	Rathi Prasad	Received

120-P1	Practicalities of Bisphosphonate Use in UK Paediatric Tertiary Centres	Victoria Price	Received

121-P1	Computer-assisted diagnosis of dyschondrosteosis based on skeletal X-ray geometry.	Gianpaolo De Filippo	Received

122-P1	Bisphosphonates therapy in girls with Rett syndrome and bone fragility	LAMBERT ANNE-SOPHIE	Received

123-P1	Skeletal manifestations in APECED	Saila Laakso	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

125-P1	SPECTRUM OF THE GENETIC DEFECTS IN HYPOPHOSPHATEMIC RICKETS IN A GROUP OF TURKISH CHILDREN	Sezer Acar	Received

126-P1	Impact of intercurrent illness on calcium homeostasis and hypoparathyroidism management	Amish Chinoy	Received

127-P1	Transient pseudohypoaldosteronism and failiure to thrive in a 5-month-old infant	Hae Soon Kim	Received

128-P1	Childhood Cancer Survivors (CCS) are at High Risk of Reduced Bone Mass during Bone Mass Accrual	DI IORGI NATASCIA	Received

130-P1	Triple X Syndrome: An Evaluation of Bone Mineral Status and Metabolism	Stefano Stagi	Received

131-P1	Frequency of recessive osteogenesis imperfecta in a Turkish cohort and genetic causes	Saygin Abali	Received

132-P1	Spinal and forearm bone mineralization in adolescents with Klinefelter syndrome.	jean de schepper	Received

133-P1	Treatment with Zoledronic Acid in children with Duchenne Muscular Dystrophy.	Irene Fernandez Viseras	Received

135-P1	Low bone mineral density in adolescents with leukemia after hematopoietic stem cell transplantation	cho wonkyoung	Received

136-P1	Growth characteristics of a girl with multicentric carpo-tarsal osteolysis caused by novel mutation in the MAFB gene	Lenka Dusatkova	Received

137-P1	Treatment Experience And Long-Term Follow-up Data in Two Severe Neonatal Hyperparathyroidism Cases	Senay Savas-Erdeve	Received

138-P1	Biochemical parameters associated with serum intact FGF23 levels in patients with X-linked hypophosphatemic rickets	Takuo Kubota	Received

139-P1	Dental effects of intravenous bisphosphonate when administered in early infancy	margaret zacharin	Received

140-P1	Bone mass and vitamin D status in children and adolescents with generalized epidermolysis bullosa	Luiz Claudio Castro	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

142-P1	Effect of Bisphosphonates and Denosumab on trabecular bone: Results of a pilot study in children with Osteogenesis imperfecta.	Mirko Rehberg	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

144-P1	Effects of phylloquinone and magnesium on ATDC5 prechondrocytes	Adalbert Raimann	Received

145-P1	To study the efficacy and safety of growth hormone (GH) therapy in children with pycnodysostosis	Zainaba Mohamed	Received

146-P2	Bone mineral status and metabolism in patients with Williams-Beuren Syndrome	Stefano Stagi	Received

147-P2	The beneficial effect of cinacalcet on the treatment of vitD resistant rickets	Aysehan Akinci	Received

148-P2	A PRELIMINARY REPORT ON BODY COMPOSITION PROFILE OF YOUNG PATIENTS WITH CHRONIC HEMOLYTIC CONDITIONS.	Artemis Doulgeraki	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

150-P2	Prevalence of Vitamin D Deficiency in Haitian Infants and Children	Julia von Oettingen	Received

151-P2	Progressive development of PTH resistance in patients with maternal GNAS inactivating mutations	Asmaa Mamoune	Received

152-P2	Effect of Hydroxyurea Therapy on Growth Parameters in Older Children with Sickle Cell Disease	doaa khater	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

154-P2	Comparison of Two Different Stoss Therapy Doses in Children with Vitamin D Deficiency or Insufficiency without Rickets	Cemil Kocyigit	Received

155-P2	Bisphosphonate Treatment of Hypercalcemia in a Child with Jansens Metaphyseal Chondrodysplasia	Erin Sharwood	Received

156-P2	Physical exercise level is associated to peak bone mass in undergraduate students.	Deisi Maria Vargas	Received

157-P2	A CASE WITH LETHAL PERINATAL HYPOPHOSPHATASIA	SEL&304;N ELMAO&286;ULLARI	Received

158-P2	Anthropometric and Nutritional Parameters in Egyptian Children with Osteogenesis Imperfecta: Effect of Zoledronic Acid Therapy	Rasha Hamza	Received

159-P2	Low bone mineral density in adolescents with joint hypermobility	Shadab Salehpour	Received

160-P2	Fractures In Children With Type 1 Diabetes Are Associated With Poorer Bone Mineral Status and Glycaemic Control	Suet Ching Chen	Received

161-P2	Identification of predictor factors of growth outcome in children with hypophosphatemic rickets	Silvia Marin	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

163-P2	Bone health index is low in children with growth hormone deficiency and improves with growth hormone treatment	Joanne Blair	Received

165-P2	Bone health and metabolic syndrome in childhood cancer survivors	Ju Young Yoon	Received

166-P2	Diversity in phenotype of 2 siblings with X-linked hypophosphatemic rickets due to PHEX mutation	Aleksandra Rojek	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

168-P2	A case of genetically proven carbonic anhydrase II deficiency	Zdravka Todorova	Received

169-P2	RICKETS AS PRECOCIOUS SIGN OF CELIAC DISEASE: THE ROLE OF VDR POLYMORPHISMS	Maria Cristina Maggio	Received

170-P2	Clinical and genetic analysis of five patients with vitamin D-dependent rickets type 1A	Bulent Hacihamdioglu	Received

171-P2	about a case of a family of pycnodysostose	rouabah niroud	Received

172-P2	Potential Role of Vitamin D in Pathogenesis of Acute Rheumatic Fever	Huseyin Demirbilek	Received

173-P2	Bartter syndrome with bone-destroying hyperparathyroidism (BSHPT): about two cases, genetically proved, with long-lasting follow-up	Jacques Weill	Received

174-P2	Management of Hypoparathyroidism: Follow up of 20 Patients	Sukran Darcan	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

176-P2	A case: Hydrocephalus secondary to suprasellar arachnoid cyst with reset osmostat and Isolated Growth Hormone Deficiency	Erdal Kurnaz	Received

177-P2	Cinacalcet Treatment in a Child With Concurrent Juvenile Idiopathic Arthritis and Hypocalciuric Hypercalcemia	Bulent Hacihamdioglu	Received

179-P2	BISPHOSPHONATE USE FOR CONTROL OF CHRONIC SEVERE BONE PAIN IN CHILDREN WITH MALIGNANCY ASSOCIATED BONE INVOLVEMENT	margaret Zacharin	Received

180-P2	Renal tubular acidosis causing severe growth delay and rickets in two siblings in Haiti	Dearthlie Bernadea	Received

181-P2	PSEUDOHYPOPARATHYROIDISM TYPE Ib ASSOCIATED TO ASSISTED REPRODUCTIVE TECHNOLOGIES: CASE REPORT.	Monica Fernandez	Received

182-P2	Primary hyperparathyroidism- a cause of metabolic syndrome in children?	Amalia Ioana Arhire	Received

183-P2	Hyperphosphatemic familial tumoral calcinosis: novel indication to sevelamer carbonate	Noemi Auxiliadora Fuentes-Bolaños	Received

185-P2	Multifocal osteonecrosis after short term methylprednysolon therapy:Case report	Aferdita Kumaraku	Received

186-P2	UNCLEAR ORIGIN OF AVASCULAR NECROSIS - CLINICAL CASE	Eremciuc Rodica	Received

187-P2	Is NOTCH- Sonic Hedgehog signalling pathway the missing link between Hajdu-Cheney syndrome and syringomyelia?	Prashant Patil	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

189-P2	about a case of dwarfism idiopathic	rouabah niroud	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

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

192-P1	Diagnostic features of lipodystrophy in children with type 1 diabetes	Svitlana Chumak	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

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

195-P1	Two patients with HADH (SCHAD) hyperinsulinism without detectable 3-hydroxybutyrylcarnitine/ 3-hydroxyglutarate.	Susanne Weiss	Received

196-P1	Development of Type 1 diabetes in a child with inherited CD59 deficiency treated with eculizumab	Serkan Bilge Koca	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

198-P1	NEONATAL DIABETES, GALLBLADDER AGENESIS AND CHOLESTATIC GIANT CELL HEPATITIS: A NOVEL HOMOZYGOTE MUTATION IN PDX-1 GENE	Ahmet Ozdemir	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

200-P1	Driving paediatric diabetes care forward in the UK: Improvements in outcomes in the North West following national initiatives	Helen Moore	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

202-P1	SCREENING FOR AUTONOMIC NEUROPATHY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS	Charalampos Tsentidis	Received

203-P1	Diabetes Mellitus caused by bone marrow transplantation and total body irradiation experience from a regional single centre.	Toby Candler	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

205-P1	Are we screening appropriate age group for early diagnosis of Cystic Fibrosis Related Diabetes (CFRD) in UK?	arundoss gangadharan	Received

206-P1	When to screen for Coeliac disease in children with Type 1 Diabetes Mellitus: the controversy	Ayo Ajanaku	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

209-P1	Association between hypothalamus-pituitary adrenal axis activity and anxiety in prepubertal children with Type 1 diabetes	Pascal Barat	Received

210-P1	Screening for liver disease in children and adolescents with type 1 diabetes mellitus: a cross-sectional analysis	Kummer Sebastian	Received

211-P1	Exploration of social network, social integration, and socioeconomic status in families with young children with type 1 diabetes.	Angela Galler	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

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

214-P1	Analysis of short-term efficacy of MiniMed 640G with SmartGuard in pediatric patients with type 1 diabetes	Beatriz Villafuerte	Received

215-P1	Influence of -cell autoimmunity on cystic fibrosis related diabetes mellitus - a DPV registry analysis	Michael Wurm	Received

216-P1	Thyroid and islet autoantibodies predict autoimmune thyroid disease already at diagnosis of type 1 diabetes	Berglind Jonsdottir	Received

217-P1	Hemolysis in a girl with type 1 diabetes mellitus and glucose-6-phosphate dehydrogenase deficiency	Lele Hou	Received

218-P1	Clinical characteristics and molecular analysis of patients with neonatal diabetes	ZEHRA YAVAS ABALI	Received

219-P1	Impact of continuous glucose monitoring system on therapy of cystic fibrosis related diabetes in children and young adults	Sladjana Todorovic	Received

220-P1	Effect of Allopurinol Versus Angiotensin Converting EnzymeInhibitors in Decreasing Microalbuminuria in Type 1 Diabetic Patients	Nancy Elbarbary	Received

221-P1	Continuous glucose monitoring and hypoglycemia unawareness in children and adolescents with type 1 diabetes	Damla Goksen	Received

222-P1	Transient, neonatal hyperinsulinemic hypoglycemia may be monogenetic, not only secondary to fetal life events	Louise Olesen	Received

223-P1	The Relationship Between The Serum Irisin Levels And The Metabolic Control In Adolescents With Type 1 Diabetes	Aysegl Yksel	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

227-P1	Rising of type 1 diabetes mellitus incidence in Chilean children between 2006 and 2014.Final results.	CAROLINA PAZ GARFIAS VON FURSTENBERG	Received

228-P1	Frequency and Risk Factors of Depression in Type 1 Diabetes in a Developing Country.	doaa khater	Received

229-P1	PHENOTYPIC VARIABILITY OF IDENTICAL MUTATIONS IN THE ABCC8 GENE IN TWO FAMILIES	Klara Rozenkova	Received

231-P1	A Rare Form of Insulin Resistance with Pseudoacromegaly	Stephen Stone	Received

232-P1	Extrahepatic biliary atresia in combination with toxic cholestasis due to Glibenclamide in a case of neonatal diabetes	Thomas Kapellen	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

234-P1	Assessment of ed carbohydrate parameters in children exposed to gestational diabetes in utero.	Ma&322;gorzata Wilk	Received

235-P1	The Genetic causes and Phenotypic Characteristics of Egyptian patients with Neonatal Diabetes Mellitus	Rasha Elkaffas	Received

236-P1	Does adherence to a high HbA1c policy improve outcomes in a paediatric diabetic clinic population?	Rachel Beckett	Received

237-P1	The prevalence of diabetic ketoacidosis in children with new-onset type 1 diabetes mellitus.	Elzbieta Niechcial	Received

238-P1	Correction of carnitine deficiency (CD) in children with recent onset Type 1 diabetes (T1D)	castell annelaure	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

240-P1	Effect of vitamin D supplementation on lipid profile in vitamin D deficient T1D patients with dyslipidemia	Noha Musa	Received

241-P1	Renal functional reserve in children with Type 1 diabetes	Vera Zdravkovic	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

243-P1	ASSOCIATED AND FAMILIAL AUTOIMMUNITY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1DM)	Martha Papadopoulou	Received

244-P1	Factors affecting dyslipidaemia in children and young people with Type 1 diabetes mellitus: A multicentre study	Swathi Upadrasta	Received

246-P1	Wolcott Rallison syndrome due to a novel mutation in EIF2AK3 gene.	vikram bhaskar	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

248-P1	GCK mutations in Chinese MODY2 patients: a family pedigree report and review of Chinese literature.	Chunlin Wang	Received

249-P1	AUTOIMMUNE LIMBIC ENCEPHALITIS ASSOCIATED WITH TYPE 1 DIABETES MELLITUS	esra dger	Received

251-P1	Metabolic impairments among adult survivors of paediatric abdominal and pelvic tumours in the St. Jude Lifetime Cohort Study	Carmen Wilson	Received

252-P1	Clinical case of a 10-year-old girl with papillomatosis due to severe insulin resistance type A	Elizaveta Orlova	Received

253-P1	Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome	Gonul Catli	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

255-P1	TRANSIENT NEONATAL DIABETES MELLITUS IN HANOI, VIETNAM: CLINICAL FEATURE AND OUTCOME	Ngoc CanThi Bich	Received

256-P1	The incidence of type 1 diabetes in the pediatric population in Pomeranian region in Poland.	Agnieszka Brandt	Received

257-P1	Health-related quality of life and its associated factors in children with Type 1 Diabetes Mellitus	Marta Murillo-Valles	Received

258-P1	POSSIBLE MONOGENIC DIABETES INCLUDING MODY IS HIGHLY PREVALENT IN KOREAN CHILDREN WITH DIABETES MELLITUS	JungEun Moon	Received

259-P1	Phenotype and clinical course of diabetes mellitus in individuals with pancreatic hypoplasia due to a PTFA enhancer mutation	Evangelia Panou	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

261-P1	Johansson-Blizzard Syndrome with Pan-hypopituitrism, Type 2 Diabetes and Pancreatic insufficiency : Effect of Treatment	Ashraf Soliman	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

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

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

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

268-P2	A patient with a rare monogenic diabetes syndrome	VIMAL MAVILA VEETIL	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

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

272-P2	A Case Report of Wolfram Syndrome due to a novel homozygous mutation in WFS1 gene	Meltem TAYFUN	Received

273-P2	Lower Basal Insulin Dose - Better Control in Type 1 Diabetes	David Strich	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

276-P2	The Best Practice Tariff for Paediatric Diabetes Care within England: A District General Experience	Kate Harvey	Received

277-P2	Prevalence of cardiovascular risk factors and obesity in youth with type 1 diabetes in Lithuania	Ingrida Stankute	Received

278-P2	Childhood type 1 diabetes (T1D) management with e-learning through self-educational tools	Pierre Bougnères	Received

279-P2	Mucormycosis and Type 1 Diabetes: A Case Report	Erdal Eren	Received

280-P2	Insulin pump therapy in Type 1 Diabetes: The Indian experience	MANPREET SETHI	Received

281-P2	Child with mutation in GATA 6 gene case report.	Agnieszka Brandt	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

283-P2	Continuous glucose monitoring can alleviate parental fear of hypoglycaemia in children with type 1 diabetes mellitus.	Helen Moore	Received

285-P2	Permanent neonatal diabetes by gene mutation kcnj11. Evolution and treatment after three years with sulphonylureas	Maria Angeles Santos Mata	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

287-P2	Diabetic ketoacidosis risk factors in the initial presentation of type 1 Diabetes mellitus in children and adolescents.	Teresa Borges	Received

288-P2	Prevalence of polycystic ovary symdrome and its clinical profile in young females with type 1 diabetes mellitus	PREETI DABADGHAO	Received

290-P2	Wolcott-Rallison syndrome: clinical case presentation	Viktoriya Furdela	Received

291-P2	The story of a de novo heterozygous HNF1A mutation	Abirami Namasivayam	Received

292-P2	Effect of packed cell transfusion on blood glucose concentrations in Beta Thalassemia Major (BTM).	Ashraf Soliman	Received

293-P2	Impact of demographic factors on Diabetic Ketoacidosis occurrence at Type 1 Diabetes onset in childhood	Flora Tzifi	Received

294-P2	Differences in Hba1c among different ethnicities; is it just a matter of mean glycaemia?	Alessandra Cocca	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

296-P2	Diabetes a rare complication of ataxic telangiectasia presenting in childhood	Sereesha Veleshala	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

298-P2	INSULIN RESPONSE AT STANDARD GLUCOSE LOAD IN CHILDREN WITH NORMAL, LOW AND EXCESSIVE BODY MASS	Tetyana Chaychenko	Received

299-P2	INITIAL PRESENTATION OF SUBJECTS WITH TYPE 1 DIABETES: A CHANGE IN SPECTRUM	Mathew John	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

301-P2	HbA1C and IGF-1 levels in diabetic children treated with Vitamin D	Elham Hashemi	Received

302-P2	LONG-TERM FOLLOW-UP OF NON-DIABETIC OBESE CHILDREN AND ADOLESCENTS TREATED WITH METFORMIN	Meliksah Keskin	Received

303-P2	Understanding the molecular and genetic basis of complex syndromes of diabetes mellitus	Melissa Riachi	Received

304-P2	Cardiovascular Risk and Long Term Follow-up of Turkish Children with Type 2 Diabetes: Single Center Experience	AYLA GUVEN	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

306-P2	Maturity-Onset Diabetes of the Young (MODY): tracking and clinical follow-up	Arthur Bezerra	Received

307-P2	Evaluation Of Autoimmune Thyroiditis Development On Onset And During Follow Up In Cases With Type 1 Diabetes Mellitus	Dilek Emine	Received

308-P2	The autoimmune hypothesis for acute bilateral cataract in type 1 diabetes	DIMITRIOS T. PAPADIMITRIOU	Received

309-P2	Clinical Characteristics of Latent Autoimmune Diabetes in Youth (Type 1.5 DM)	Jeesuk Yu	Received

310-P2	Diabetic Ketoacidosis: Clinical features and Precipitating Factors at DEMPU	Amany Ibrahim	Received

311-P2	Diabetes Distress in Adolescents and Young Adults with Type 1 Diabetes	Ingrida Stankute	Received

312-P2	A NOVEL GLUCOKINASE GEN MUTATION: MODY TYPE-2 CASE	Aslihan Arasli Yilmaz	Received

313-P2	Congenital Hyperinsulinism in a resource limited setting: Overcoming barriers towards a survival path	Joel Dipesalema	Received

314-P2	Vitamin D levels and relations with clinical and laboratory findings in children with newly diagnosed type 1 diabetes	Gulay Karaguzel	Received

316-P2	Cystic Fibrosis Related Diabetes	Afaf AlSagheis	Received

317-P2	Type 1 diabetes in childhood:an 8 year experience	SOTIRIA GIANNOPOULOU	Received

318-P2	A Rare Reason of Type 2 Diabetes: Alstrm Syndrome	onur akin	Received

320-P2	Hyperglycaemia in a boy of 13 years old: Not always Type 1 Diabetes Mellitus. A case report	Zacharoula Karabouta	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

322-P2	Clinical and laboratory characteristics of children and adolescents with type 1 Diabetes Mellitus.	Olcay Evliyaoglu	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

324-P2	Glargine versus Detemir insulin during the Honeymoon phase in a child with type1 diabetes mellitus	Ashraf Soliman	Received

325-P2	DIABETIC KETOACIDOSIS AND MULTIPLE ORGAN FAILURE SYNDROME: A CASE STUDY	Bui Thao	Received

326-P2	Neonatal diabetes associated with transaminitis in a growth retarded infant	Kiran Parbhoo	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

328-P2	RAPID ACTING INSULIN ANALOGUE TREATMENT IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS; INSULIN GLULISINE EXPERIENCE	Sevinc Odabasi Gunes	Received

332-P2	Evaluating the impact of the diagnosis and management of children with type 1 diabetes on parents/carers	Ciara McCormick	Received

333-P2	Association between Socioeconomic Status and Glycemic control inType 1 Diabetes Mellitus	Prashant Patil	Received

334-P2	Minimally invasive surgical interventions in the treatment of primary persistent hyperinsulinemic hypoglycemia of infancy.	Fahimeh Soheilipour	Received

335-P1	Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene	Johanna Knskoski	Received

336-P1	Polycystic Ovary Syndrome in Adolescence: new therapeutic approach with Inositol and Alpha-Lipoic Acid.	maria laura iezzi	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

338-P1	Primary Ovarian Insufficiency in Childhood Cancer Survivors: A Report from the St. Jude Lifetime Cohort	Wassim Chemaitilly	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

340-P1	Intrauterine growth restriction (IUGR) affects postnatal testis maturation in rats	Valentina Pampanini	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

342-P1	Genotype-phenotype correlation of NR5A1/SF1- mutations by functional in-vitro studies	Rebekka Astudillo	Received

343-P1	Evolution of body composition and bone mass in transgender adolescents treated with pro- or anti-androgenic progestins.	Lloyd Tack	Received

344-P1	Sertoli cell function during chemotherapy in pediatric patients with acute lymphoblastic leukemia (ALL).	Romina P. Grinspon	Received

345-P1	Accuracy of pelvic MRI in evaluating internal genitalia in patients with Disorders of Sex Development	Linda Mahfouz	Received

346-P1	Using public databases, virtual controls and geolocalization to search for Environmental correlates of Hypospadias	BOUGNERES Pierre	Received

347-P1	The International AGD Consortium: a multi-center study of 3939 infants and children with anogenital distance measurements	Marie Lindhardt Johansen	Received

348-P1	Silent Mutations in Exonic Region of Androgen Receptor Gene Related to Androgen Insensitivity Syndrome	Rafael Loch Batista	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

350-P1	Clinical history and high prevalence of gonadal tumor in 14 patients with 46 XY pure gonadal dysgenesis	Claire Sechter	Received

352-P1	A multicenter study on long-term outcomes in 59 males with 45,X/46,XY mosaicism	Marie Lindhardt Johansen	Received

353-P1	Familial testotoxicosis: outcome and possible relation to testicular malignancies	Idske Kremer Hovinga	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

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

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

357-P1	Changes in adrenal steroids during puberty suppression and cross sex hormone treatment in gender dysphoric adolescents	Sebastian Schagen	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

359-P1	Feasibility study for avoiding early surgery in girls with 21-hydroxylase deficiency (21OHD)	Pierre Bougnères	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

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

362-P1	Aromatase activity is disrupted by mutations in P450 oxidoreductase (POR)	Shaheena Parween	Received

363-P1	Mosaic Xq Partial Duplication Leading to Virilisation of an Adolescent Female	Elizabeth Baranowski	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

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

366-P1	Consecutive lynestrenol and cross-sex hormone treatment in biological female adolescents with gender dysphoria: a retrospective analysis.	Lloyd Tack	Received

367-P1	Ovarian reserve assessment in girls and women after hematopoietic stem cell transplantation (HSCT) treatment underwent in childhood	Anna Wedrychowicz	Received

368-P1	Precocious/early and accelerated puberty in a boy with a homozygous R192C mutation in CYP19 (aromatase) gene	Mariana Costanzo	Received

369-P1	Long term follow up of patients with 46,XY partial gonadal dysgenesis accordingly gender assignment	Nathalia Gomes	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

371-P1	Androgen profile differs to adults in adolescent girls with polycystic ovary syndrome (PCOS)	Joanne Blair	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

373-P1	Compound heterozygous C10orf2 mutations in a Japanese patient with 46, XX ovarian failure and deafness	Keisuke Nagasaki	Received

374-P1	GATA transcription factors in Testicular Adrenal Rest Tumours	Manon Engels	Received

375-P1	Can we standardize sex assignment in 45,X/46,XY mixed gonadal dysgenesis?	Johanna Viau Colindres	Received

376-P1	Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia: A Case Report	Hale Tuhan	Received

378-P1	Randomized controlled study comparing vitamin D and omega 3-fatty acids supplementation in adolescents with polycystic ovary syndrome	Flora Bacopoulou	Received

379-P1	Health-related Quality of Life and Psychological Wellbeing in Adults with Disorders of Sex Development (DSD)	Elena Bennecke	Received

380-P1	Association of Genetic Polymorphisms around the LIN28B Gene and Idiopathic Central Precocious Puberty Risks among Chinese Girls	Ruimin Chen	Received

381-P1	Psychological Outcomes and Quality of Life of patients with non-CAH Disorders of Sex Development	Nalini M Selveindran	Received

382-P1	Normalization of Ovulation Rate in Adolescent Girls with Hyperinsulinemic Androgen Excess	Lourdes Ibañez	Received

383-P2	Thyroid autoimmunity in adolescent girls with polycystic ovary syndrome - pilot study.	Agnieszka Zachurzok	Received

384-P2	The efficacy and safety of gonadotropin-releasing hormone analogue treatment to suppress puberty in gender dysphoric adolescents	Sebastian Schagen	Received

385-P2	A familial form of DSD due to NR5A1 mutation in a father and his son	Claire-Lise GAY	Received

386-P2	High prevalence of SGA in patients with disorders of sexual development (DSD), especially idiopathic 46,XY DSD	Asmahane Ladjouze	Received

387-P2	Questionnaire surveys targeting Japanese pediatric endocrinologists regarding reproduction in pediatric and adolescent cancer patients	Yoko Miyoshi	Received

388-P2	Fertility outcomes after childhood onset hypothalamic hypogonadism	margaret Zacharin	Received

389-P2	Persistent Mullerian Duct Syndrome with transverse testicular ectopia: a novel AMH receptor mutation	zlem korkmaz	Received

390-P2	Three Cases of NR5A1 (SF1) gene mutations in DSD patients	Nadezda Raygorodskaya	Received

391-P2	Sertoli-Leydig Cell Tumor as a rare cause of hirsutism in a young adolescent	Saskia van der Straaten	Received

392-P2	Identification of an AR mutation in Klinefelters Syndrome during Evaluation for Penoscrotal Hypospadias	Sezer Acar	Received

393-P2	Assessment of sexual identity in patients with congenital adrenal hyperplasia	Maryam Razzaghy-Azar	Received

394-P2	Duct ectasia, a rare complication of gynaecomastia	Noemi Auxiliadora Fuentes-Bolaños	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

396-P2	Hypogonadotropic hypogonadism in a girl with 2p11.2 2q12.1 duplication	Stefano Stagi	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

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

399-P2	Diagnosis of PCOS in adolescents using MRI	Maxime Fondin	Received

400-P2	Novel CYP17A1 mutation and CYP21 mutations in two siblings	Emregl Isik	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

404-P2	Case report of a girl with secondary amenorrhea associated with aurantiasis cutis	Ralph Decker	Received

405-P2	Maternal ovarian luteoma causing complete virilization of a female fetus	Carla Minutti	Received

406-P2	The experience of GAIA (Abuse Childhood and Adolescence Group) AOU MEYER	Stefano Stagi	Received

407-P2	State of knowledge of late endocrinological effects of hematological patients who has undergone chemotherapy	Ewa Barg	Received

409-P2	Analysis of clinical manifestations and gene mutations of 5a-reductase type 2 deficiency in 16 cases	Lele Hou	Received

410-P2	Unusual differential diagnosis of Hyperandrogenism in Adolescent female treated for Polycystic Ovarian Syndrome	Carolina Di Blasi	Received

411-P2	Phenotypic and hormonal variability in 46,XY subjects with SF-1 mutations	Natacha Dillies	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

413-P2	Two patients presenting the extremes of the phenotypic spectrum of 5 alfa reductase deficiency; one with at new mutation.	Niels Birkebaek	Received

414-P2	Disorders of Sex Development 45,X/46,XY: Clinical and Laboratory Characteristics of Patients	Ekaterina Sannikova	Received

415-P2	Reproductive function of central precocious puberty in girls: A systematic review	JiHyun Kim	Received

416-P2	Ovotesticular Disorder of Sex Development (OT- DSD) among Egyptian DSD patients	mona mekkawy	Received

417-P2	Cytogenetic Study of Sex Chromosomal abnormalities in Egyptian DSD patients	inas Mazen	Received

419-P2	XLAG SYNDROME CASE ACCOMPANYING A NEW ARX MUTATION AND HAS A INTERHEMISPHERIC CYST	Ahmet Ozdemir	Received

420-P2	Congenital adrenal lipoid hyperplasia in a 30-year-old female with a tall stature	Yasunori Wada	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

422-P2	LATE CLINICAL PRESENTATION, BIOLOGICAL ASSESSMENT AND MANAGEMENT OF PAIS IN A DEVELOPING COUNTRY	Daniela GORDUZA	Received

423-P2	SISTERS WITH 46XY GONADAL DYSGENESIS AND GONADOBLASTOMA	FOTEINI PETYCHAKI	Received

424-P2	Follow-up to adulthood of two 46,XY siblingswith 5-alpha reductase deficiency and different sex of rearing	Lyne Chiniara	Received

425-P2	Constitutional delay of puberty: clinical and hormonal characteristics of patients	Lyubov Osipova	Received

426-P2	Comparison between serum vitamin D levels in precocious pubertal girls and normal girls	Joon woo Baek	Received

427-P2	Complete virilization without salt wasting in a 7-y old Haitian child with congenital adrenal hyperplasia	Billy Roosler Telcide	Received

428-P2	Hematocolpos revealed by non-cyclic lower-back pain in a pre-menarcheal girl	Nathalie Ly	Received

429-P2	Novel AMH and AMHR-II Mutations in Two Egyptian Families with Persistent Mullerian Duct Syndrome	aya elaidy	Received

430-P2	Study of Genetics of Human Disorders of Sexual Development. Research Project.	Markosyan Renata	Received

431-P2	46XX male syndrome	Markosyan R	Received

432-P2	45,X/47,XYY chromosomal mosaicism as a cause of 46, XY Disorder of Sex Development	ANIK AHMET	Received

433-P2	46, XY complete gonadal dysgenesis with late diagnosis	Vilhelm Mladenov	Received

435-P2	An Infant with 49XXXXY Syndrome; A case report from Sri Lanka.	Chamidri Naotunna	Received

436-P2	MIXED GONADAL DYSGENESIS: Patients from Instituto da Criana, HC-FMUSP	Marianna Ferreira	Received

438-P2	HYPOGONADOTROPIC HYPOGONADISM IN A PATIENT WITH VANISHING TESTIS SYNDROME CASE REPORT	Zsuzsanna Szanto	Received

439-P2	17 alpha hydroxylase, 17-20 lyase deficiency, a case with hypocalcemic symptoms	esra dger	Received

440-P2	An uncommon case of adolescent with POF.	Sara Queirolo	Received

441-P2	Trisomy 9 Syndrome in an Infant with Ambiguous Genitalia	parasto rostami	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

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

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

445-P1	The impact of activating PIK3CA mutations and PTEN haploinsufficiency on human adipocyte phenotype and biology	Franziska Kner	Received

446-P1	Bioinactive leptin is not frequently detected in severe early onset childhood obesity	Juraj Stanik	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

448-P1	Laparoscopic sleeve gastrectomy in adolescents with morbid and dynamic obesity. A controlled monocentric study.	Gianpaolo De Filippo	Received

449-P1	EFICACY, SAFETY AND METABOLIC EFFECTS OF CARBOHYDRATE RESTRICTION IN THE TREATMENT OF OBESE ADOLESCENTS	Gabriel Ángel Martos-Moreno	Received

450-P1	SEVERE HYPERTRIGLYCERIDEMIA IN PEDIATRIC ONCOLOGY PATIENT	Grau Gema	Received

452-P1	High predictability of impaired glucose tolerance by combining diagnostic parameters in obese children	Corjan de Groot	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

454-P1	INFLUENCE OF TELEVISION VIEWING DURING MEALS ON EATING PATTERNS	Rosaura Leis	Received

455-P1	7-year follow-up of mothers from a randomized controlled trial of exercise in pregnancy and their offspring	Valentina Chiavaroli	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

457-P1	Premature adrenarche and metabolic risk: differences by gender	Veronica Mericq	Received

458-P1	Association of miR-34a and mir-149 with obesity and insulin resistance in obese children and adolescents	Mitra Nourbakhsh	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

461-P1	Adiponectin and IL-6 in simple childhood obesity with and without hepatic steatosis	Stefano Stagi	Received

462-P1	Determinants of advanced bone age in childhood obesity	Corjan de Groot	Received

463-P1	Exposure to Phthalates Is Associated with Overweight or Obesity in 4-Year-Old Children	Jieun Lee	Received

464-P1	Central obesity among European preschool children: The ToyBox-Study	Sonya Galcheva	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

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

468-P1	Association of fasting triglycerides to high-density lipoprotein ratio with risk of metabolic disorders in children	Andrea Paola Rojas Gil	Received

469-P1	Assessment of Adherence to Mediterranean diet during a weight loss intervention in children with cardiometabolic risk	Lydia Morell	Received

470-P1	Brain structure, utive function and appetitive traits in adolescent obesity	Corjan de Groot	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

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

473-P1	Inherited duplication (X) (p11.4) associated with obesity, autoaggressive behaviour and delayed speech development	Carsten Doeing	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

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

476-P1	Polysomnography in obese children with and without Prader-Willi syndrome	Elena Bogova	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

480-P1	Associations of different appetite hormones with physical activity and cardiorespiratory fitness in adolescent boys with different BMI values	Vallo Tillmann	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

482-P1	Changes in urine and plasma metabolomics profiles after a lifestyle intervention program in obese prepubertal children.	María Jesús Leal Witt	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

484-P1	Fetuin-A as an Alternative Marker for Insulin Resistance and Cardiovascular Risk in Prepubertal Children	Yeon Joung Oh	Received

485-P1	What are early predictors of impaired glucose tolerance in children born SGA?	Indre Petraitiene	Received

486-P1	Multidisciplinary Intervention Programme in Childhood Obesity - Review of Service	Jeremy Jones	Received

487-P1	Hypercholesterolemia in childhood: how the response to diet could lead to diagnosis. Lesson from a case-report.	Barbara Predieri	Received

488-P1	GLUCOSE METABOLISM IN CHILDREN WITH PRADER-WILLI SYNDROME (PWS): THE EFFECT OF GH THERAPY	Danilo Fintini	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

490-P2	MATSUDA INDEX IN CORRELATION WITH CLINICAL INDICATORS OF INSULIN RESISTANCE IN CHILDREN AND ADOLESCENTS	PETYCHAKI FOTEINI	Received

491-P2	Anthropometric, biological and imagistic methods for assessing the cardiovascular risk in obese children	Ramona Stroescu	Received

492-P2	TRENDS OF NUTRITION OF UKRAINIAN CHILDREN FROM KHARKIV REGION: TENDENCY TO OVERWEIGHT, DEHYDRATION AND IMPAIRED SOCIAL ADAPTATION	Tetyana Chaychenko	Received

493-P2	Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents	Korcan Demir	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

495-P2	The cutoff values of indirect indices for measuring insulin resistance in Korean children and adolescents	Heon-Seok Han	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

497-P2	CARDIOMETABOLIC EFFECT OF SUGAR-SWEETENED BEVERAGES REDUCTION IN OBESE CHILDREN	Júlia Galhardo	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

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

500-P2	Prevalence and characteristics of polycystic ovary syndrome in obese adolescents	Marina Ybarra	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

502-P2	METABOLIC SYNDROME IN PREPUBERTAL OBESE CHILDREN: INCLUSION OF THE TRIGLYCERIDE/HDL RATIO AS AN ALTERNATIVE DIAGNOSTIC CRITERION	CARLA BOQUETE	Received

503-P2	The relationship between subclinical hypothyroidism and iodine deficiency, serum leptin levels and metabolic syndrome in obese children	Cemil Kocyigit	Received

504-P2	Analysis of circulating miRNAs in obese children born small for gestational age	Maria Felicia Faienza	Received

505-P2	Irisin and abdominal obesity in preschool age.	Mina Lateva	Received

506-P2	Long term outcomes after hospital based, life-style weight loss intervention during childhood	Toby Candler	Received

507-P2	Implications of Insulin resistance in obese and overweight children: A cohort analysis	Sangita Yadav	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

509-P2	Which marker is the most reliable one for the detection of NAFLD in outpatient clinic?	Elif zsu	Received

510-P2	Nonalcoholic fatty liver disease: Evolution after one year of follow-up with different therapies	Maria Angeles Santos Mata	Received

511-P2	Lifestyle Survey of Doctors, Medical Residents and Medical Students in Latvia	Jurgita Gailite	Received

512-P2	Weight status in children at 8 years: a prospective cohort study	ISOLINA RIANO-GALAN	Received

513-P2	Low birth weight is not associated with increased risk of metabolic syndrome in obese children and adolescents.	Elena Inzaghi	Received

514-P2	Prader Willi Syndrome in Brazil: 6 months follow-up in a referral center	Simone Sakura Ito	Received

515-P2	EARLY BLOOD PRESSURE ABNORMALITIES RELATED TO CARDIOVASCULAR RISK IN OBESE CHILDREN AND ADOLESCENTS	Gonzalo Herraiz	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

517-P2	Polycystic Ovarian Syndrome in a population of obese adolescents	Elowe-Gruau Eglantine	Received

518-P2	Vitamin D deficiency in obese children and the relationship with insulin resistance and Metabolic Syndrome	Irene Fernandez Viseras	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

520-P2	Preliminary findings on nutrition care competence in health care professionals using a standardized questionnaire NUTCOMP Korean version	Kieun Kim	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

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

523-P2	Body image perception changes in obese and lean children	Liudmila Viazava	Received

524-P2	Non-alcoholic hepatic steatosis in obese children and the relationship with insulin resistance	Irene Fernandez Viseras	Received

525-P2	Prevalence of melanocortin 4 receptor (MC4R) mutations in Turkish obese children	Samim zen	Received

526-P2	Prevalence of Overweight and Obesity in Childrenand Adolescents in Izmir, Western Turkey	ZLEM NALBANTO&286;LU	Received

527-P2	Evaluation of metabolic abnormalities in obese children: interest of using standardized pediatric values.	Adele CARLIER	Received

529-P2	Insulin resistance correlates to cognitive fatigue dimensions in non-diabetic obese children	Pascal Barat	Received

530-P2	VASCULAR ENDOTHELIAL GROWTH FACTOR AS THE PREDICTOR MICROANGIOPATHY IN OBESE AND DIABETIC CHILDREN	Iwona Ben-Skowronek	Received

531-P2	Associations of Serum 25-Hydroxyvitamin D and Components of the Metabolic Syndrome in an Egyptian Cohort	Amany Ibrahim	Received

532-P2	Retrospective Evaluation of The Efficiency of Metformin Therapy in Obese Children with Insulin Resistance	Hale Tuhan	Received

533-P2	Parental obesity can trigger obesity in children	shahin koohmanaee	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

535-P2	Thyroid dysfunction and formation of dyslipoproteiniaemias: gender differences in children with obesity	Olena Budreiko	Received

536-P2	How early is Insulin resistance in our Pediatric population with Metabolic syndrome	Sangita Yadav	Received

537-P2	INSULIN RESISTANCE FOR ADOLESCENTS WITH OBESITY IN LATVIA	Jurgita Gailite	Received

538-P2	Parental obesity can trigger obesity in children	shanin koohmanaee	Received

540-P2	Analysing child obesity risk factors: adenotonsillectomy	Corina Paul	Received

542-P2	Obstructive Sleep Apnea Syndrome in Early Childhood: Case Report	Beatriz Semer	Received

543-P2	25-Hydroxyvitamin D concentrations in pubertal children with obesity	Desislava Yordanova	Received

545-P2	Prevalence of acanthosis nigricans and related factors in Iranian Obese children	fatemeh sayarifard	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

547-P1	Laboratory findings of 302 patients with hyperinsulinemic hypoglycemia at hypoglycemia	Tohru Yorifuji	Received

549-P1	Congenital Hyperinsulinism in Infancy: The profiles of insulin secretory granules are markedly different in focal- and diffuse -cells	Mark Dunne	Received

550-P1	Persistent ketotic hypoglycemia as an atypical presentation of heterozygous HNF4A mutation	Daphné Cloutier	Received

551-P1	Enhanced mitochondrial densities associate with the pathobiology of -cells in Congenital Hyperinsulinism in Infancy	Mark Dunne	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

553-P1	Neonatal diabetes in Ukraine	Eugenia Globa	Received

554-P1	Clinical and Molecular Characteristics of Turkish Patients with Congenital Hyperinsulinism: A Single-Center Experience	Melek Yildiz	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

556-P1	Pancreatic Glucagon secretion is severely impaired and Somatostatin secretion unchanged in patients with Hyperinsulinaemic Hypoglycaemia	PRATIK SHAH	Received

557-P1	Six cases of congenital hyperinsulinism caused by mutations in MODY genes	karen berthelon	Received

558-P1	Cerebral outcome of children with congenital hyperinsulism	Annett Helleskov	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

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

561-P1	A case of hyperinsulinemic hypoglycemia, associated with insulin autoimmune syndrome (IAS) in 3.5 year old girl.	Elena Kuznetsova	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

563-P1	Hyponatremia in infants under 100 days old: frequently overlooked and multifactorial	Caroline Storey	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

565-P1	Different long-term neurodevelopmental outcomes in very preterm versus very-low-birth-weight infants	Jonneke Hollanders	Received

566-P1	Challenging management of Costello syndrome with severe Congenital Hyperinsulinaemic Hypoglycaemia.	Maria Guemes	Received

567-P1	Risk Factors and Clinical Features of a Large Cohort of Patients with Transient Hyperinsulinemic Hypoglycaemia.	John Reed	Received

568-P1	A rare case of neonatal hypothyroidism	Chin Kien Eyton-Chong	Received

569-P1	Maternal nutritional risk factors associated with neonatal hyperinsulinism	Mathilde Louvigné	Received

570-P2	Genotype and Phenotype of 99 Vietnamese Patients with Congenital Hyperinsulinism	Dung Vu Chi	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

572-P2	Sirolimus Therapy in Infant with Congenital Hyperinsulinemic Hypoglycemia unresponsive to diaxoside	CAROLINA PAZ GARFIAS VON FURSTENBERG	Received

573-P2	IPEX SYNDROME CAUSED BY A NOVEL MUTATION IN FOXP3 GENE: A CASE REPORT	Ngoc CanThi Bich	Received

574-P2	Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Sensitivity in Premature Neonates	Steven Ghanny	Received

575-P2	Persistent Hyperinsulinemic Hypoglycemic Of Infancy (PHHI)	Omalmir Fathalla	Received

576-P2	The Postnatal Effect of Serum Vitamin D Binding Protein on Serum Vitamin D Level	Hakan Dneray	Received

577-P2	ENDOCRINOLOGISTS HAVE A ROLE IN MODERATING ADVERSE METABOLIC CONSEQUENCES OF EARLY OVER FEEDING OF CHILDREN BORN IUGR	Margaret Zacharin	Received

578-P2	Primary hyperparathyroidism in children and adolescents: About a series of 10 patients	soumeya fedala	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

580-P2	NEWBORNS OF MOTHERS AFFECTED BY AUTOINMUNE THYROID DISEASE	María Magdalena Hawkins	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

583-P2	Neonatal failure to thrive not always a congenital adrenal hyperplasia.	Laura Kasongo	Received

584-P2	A UNIQUE IL2RA MUTATION PRESENTING AS NEONATAL DIABETES, CONGENITAL HYPOTHYROIDISM AND SEPSIS	SRINAGESH V	Received

585-P2	Change level of TRAb in newborn leads to thyroid dysfunction - case report	Beata Sawicka	Received

586-P2	Hyperthyrotropinemia of the preterm newborn: treat or not to treat?	Serena OSSOLA	Received

587-P2	Permanent neonatal diabetes mellitus due to a G32S heterozygous mutation in the insulin gene	ke Huang	Received

588-P2	Case report on hyperinsulinism/hyperammonaemia (HI/HA) syndrome: an easily treatable cause of postprandial hypoglycaemia	Sumudu Seneviratne	Received

589-P2	Severe Systemic Pseudohypoaldosteronism Type 1: 5 years of evolution	Maria Miguel Gomes	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

592-P2	Neonatal hyperparathyroidism with homozygous missense mutation in the CASR gene	Nadia Alghazir	Received

593-P1	The mechanistic role of Fibroblast growth factor 21 (FGF21) in Growth Hormone resistance secondary to chronic childhood conditions.	Jayna Mistry	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

595-P1	The diagnostic value of IGF-II, IGF-I and IGFBP-3 in Silver-Russell syndrome	Gerhard Binder	Received

596-P1	Functional in vitro characterization of two novel germinal STAT3 mutations associated with short stature, immunodeficiency and autoimmune disease.	Mariana Gutierrez	Received

598-P1	Human Phase1 clinical data of ALT-P1 (hGH-NexP) by Healthy Korean males.	Soon Jae Park	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

600-P1	The influence of recombinant human growth hormone treatment on very small embryonic/epiblast-like stem cells (VSELs)	Anna Wedrychowicz	Received

601-P1	A LIPID BASED SYSTEM FOR THE ORAL DELIVERY OF GROWTH HORMONE	Klaus Hartmann	Received

602-P1	Prediction of first year response to growth hormone treatment in neural network models	Urszula Smyczynska	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

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

605-P1	A new case of intragenic deletion in IGF1R with very mild phenotype	Ruggero Coppola	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

608-P1	Pubertal Height Gain in Females with Isolated Growth Hormone Deficiency Treated with rhGH alone or in combination with GnRHan	Voutetakis Antonis	Received

609-P1	Cognitive Abilities and Academic Achievement Among Youths With Short Stature Receiving Growth Hormone Therapy	David Sandberg	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

611-P1	IGFALS Gene Deletion in a Family with Short Stature	Belma Haliloglu	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

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

614-P1	Serum alpha-klotho levels are not informative for the evaluation of GH secretion in short children.	Cristina Meazza	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

616-P1	SERUM IGF-I, IGFBP-3 AND ALS CONCENTRATIONS AND PHYSICAL PERFORMANCE IN YOUNG SWIMERS DURING A TRAINING SEASON	Carlos Martinelli	Received

617-P1	The blood antioxidant system in adult growth hormone deficient patients after concluded childhood growth hormone therapy	Maria Vorontsova	Received

618-P1	Design and Clinical Development of TransCon Growth Hormone for Growth Hormone Deficiency	Yi Su	Received

619-P1	Mutations in PROP1 gene in combination with 47, XYY karyotype: case report	Diliara Gubaeva	Received

620-P1	Efficacy of Growth Hormone Treatment in Patients with type 1 Diabetes mellitus and Growth Hormone Deficiency	Ferah Aydin	Received

621-P1	Final height after growth hormone treatment in children with chronic renal failure	Carla Bizzarri	Received

622-P1	Major Plasma Carotenoids Levels in Growth Hormone Deficient Children	Maria Pankratova	Received

623-P1	Autosomal Dominant Growth Hormone Deficiency due to a novel mutation in the gh1 gene.	Bradley Miller	Received

624-P1	A Novel GH1 Mutation in a Family with Autosomal-Dominant Type II Isolated Growth Hormone Deficiency	fatih gurbuz	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

626-P1	Significance of IGF-I generation test in diagnosing primary and non-primary IGF-I deficiency clinical considerations	Joanna Smyczynska	Received

627-P1	Change of growth pattern and thickness of epiphyseal plate in female rats according to injected estrogen dosage.	ByungHo Kang	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

629-P1	Treatment of resistant paediatric somatotropinomas due to AIP mutation with Pegvisomant	margaret Zacharin	Received

630-P1	GH-pattern with high trophs are often found after daily sc rhGH-injection in children.	Elena Lundberg	Received

631-P1	Are the GH treatment doses in use within secretion rates of healthy children?	Elena Lundberg	Received

632-P1	The influence of Growth Hormone treatment on Fat-free Mass in Kabuki Syndrome children.	Robin Remmel	Received

633-P1	Evaluation of prepubertal patients with suspected neurosecretory dysfunction of growth hormone secretion: diagnostic steps and treatment response	Carmen Sydlik	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

635-P1	Glucagon versus clonidine stimulation for testing growth hormone secretion in children and adolescents: which is better?	Galit Asher	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

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

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

639-P1	Spanish ECOS Study Analysis: Socioeconomic Data, Adherence and Growth Outcomes with Case Studies	Steven Goodrick	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

641-P2	Hypochondroplasia (HC) treatment with Growth hormone (rGH). Actualization of pilot observations.	Pierre Bougnères	Received

642-P2	The influence of Growth Hormone treatment on the Basal Metabolism in Kabuki Syndrome children.	Robin Remmel	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

644-P2	Adverse effects after priming with testosterone in short-statured boys before growth hormone stimulation test.	Andrea Albrecht	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

646-P2	Metabolic Parameters and Glucose Homeostasis in in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting	Mahjouba ahmid	Received

647-P2	Final adult height (FAH) in patients with PROR -1 gene mutations during growth hormone long-term therapy.	Elena Nagaeva	Received

648-P2	Congenital hypopituitarism: Genotypic-phenotypic-neuroradiological correlation	Cristina Partenope	Received

649-P2	A case of hypopituitarism in a patient with Cantù syndrome	Stefano Stagi	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

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

653-P2	Improving the gold standard. The insulin tolerance test revisited.	Nikolaos Daskas	Received

654-P2	Adherence to growth hormone therapy: comparison of electronic auto-injection to non-electronic injection devices	Klaus Hartmann	Received

655-P2	Factors influencing peak GH response during insulin and clonidine stimulation tests	Ionela Pascanu	Received

656-P2	Improved growth outcomes with jet delivery of growth hormone in children are maintained over long-term treatment.	Maria Michaelidou	Received

657-P2	Septo-optic dysplasia and excellent growth with low Growth Hormone dose: our experience	Cristina Partenope	Received

658-P2	Early diagnosis and treatment of a newborn with POU1F1 mutation	Thérèse Bouthors	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

661-P2	First do no harm: growth hormone (hGH) treatment in a case of recurrent craniopharyngioma.	George-Sebastian Zmau	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

663-P2	A case of GH deficiency in a female with 3M syndrome	Stefano Stagi	Received

664-P2	Case report of SHOX gene haploinsufficiency diagnosed in early infancy	Dario Gallo	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

666-P2	USEFULNESS OF GROWTH HORMONE TRANSIENT TREATMENT SUSPENSION IN PREPUBERTAL CHILDREN TREATED WITH GROWTH HORMONE	María Martinez	Received

667-P2	Birth length, weight and head circumference of neonates with IGF-I receptor mutations	Zvi Laron	Received

668-P2	A rare cause of growth delay- Jacobsen syndrome	Georgiana Constantinescu	Received

669-P2	A GH-1 mutation diagnosed in a preadolescent obese girl with only mild reduced height	Agnès Béreau	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

671-P2	Assessing Disease and Treatment Burden for Young Children with Growth Hormone Deficiency (GHD)	Jane Beck	Received

672-P2	Long-term results of GH therapy in GH-deficient children treated in Albania	Agim Gjikopulli	Received

676-P2	Is the growth hormone deficiency the cause of short stature in Floating Harbor syndrome?	Alice Ioana Albu	Received

677-P2	LHX-4 Gene Mutation in a Boy with Hypopituitarism and Severe Congenital Myopathy	Zoran Gucev	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

680-P2	A case of Growth Hormone deficiency with combined Encephalocraniocutaneouslipomatosis(ECCL) and Jaffe-Campanacci syndrome (JCS)	Choi Eunmi	Received

681-P2	Evaluation of Growth Hormone Deficient pre pubertal children treated with Omnitrope using the AuxoLog computer program	Margarida Vasconcelos Palla Garcia	Received

682-P2	Calcaneal Apophysitis (Severs Disease) Development in a Case Using Growth Hormone	Erdal Kurnaz	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

684-P2	Growth effects of somatropin during the treatment congenital hypopituitarism in children after the start of puberty.	Olga Berseneva	Received

685-P2	Congenital Hypopituitarism and Giant Cell Hepatitis in a Two-Months-Old Boy.	Yulia Skorodok	Received

686-P2	Neonatal characteristics of GH deficiency in 107 children	soumeya fedala	Received

687-P2	Diagnostic Value of Growth Hormone Stimulation Test for Growth Hormone Deficiency in Short Children	Jeesuk Yu	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

689-P1	Novel germline mutations in DICER1 gene in patients with different pediatric hereditary tumors.	Roxana Marino	Received

690-P1	Fludrocortisone- a treatment for tubulopathy post paediatric renal transplantation: A Scottish study	Salma Ali	Received

691-P1	Neonatal diabetes and congenital hypothyroidism, a rare condition: report of 2 cases with different genetic causes.	Carolina Mendoza Fuentes	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

693-P1	IS IT CAUTIOUS TO WAIT FOR SERUM BASAL CALCITONIN LEVELS RISE IN PATIENTS WITH RET CODON C634 MUTATIONS?	Esther Gonzálezz	Received

695-P1	CANDLE syndrome a new autoinflammatory lipodystrophic disorder with challenging diagnosis and limited therapeutic options	Veselin Boyadzhiev	Received

696-P1	Variable phenotype and genetic findings in a cohort of patients with pseudohypoparathyroidism	Nadezhda Makazan	Received

697-P1	Contiguous gene syndrome involving NR0B1 (DAX1) deletion with congenital adrenal insufficiency	Roschan Salimi Dafsari	Received

698-P1	Clusters of Autoinmune Diseases in Children	Cristian Seiltgens	Received

699-P1	Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity	Cristian Seiltgens	Received

700-P2	Effects of growth hormone treatment on glucose tolerance in young adults with Prader-Willi syndrome	Stephany Donze	Received

701-P2	TPIT mutation may be involved in multiple pituitary deficiencies	Pauline Degand	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

704-P2	Autoimmune diseases and metabolic outcome in Turner syndrome comparison between 45,X0 and other X chromosome abnormalities	Yael Lebenthal	Received

705-P2	Endocrinological Disorders in children with Neurofibromatosis type 1 and Optic Pathway Gliomas	raffaella nacca	Received

706-P2	Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) managed with fluid restriction and salt supplementation	Lisa Amato	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

708-P2	Inhibition of NAMPT increases the sensitivity of leukemia cells for etoposide	Theresa Gorski	Received

709-P2	Neonatal Endocrinological Problems In Collodion Babies	Ahmet Ozdemir	Received

710-P2	Endocrine dysfunction in children and adolescents with CHARGE syndrome	Jin-Ho Choi	Received

711-P2	Growth and pubertal patterns in young survivors of childhood acute lymphoblastic leukemia	SHLOMIT SHALITIN	Received

712-P2	Clinical assessment of hypercalciuria and hypomagnesemia in patients with Bartter syndrome and Gitelman syndrome	Wenjing Li	Received

713-P2	Wolfram syndrome: Three cases	Ilkin Majidov	Received

714-P2	Autoimmune hypoparathyroidism and celiac disease: a rare paediatric association outside an Autoimmune Polyglandular Syndrome	Francesco Gallo	Received

716-P2	ENDOCRINE DISORDERS IN CHILDREN WITH THALASSEMIA MAJOR A HOSPITAL BASED RETROSPECTIVE STUDY	Swati Kanodia	Received

717-P2	15-year old girl with APS type IIIc, with post-thymectomy remission case report.	Artur Bossowski	Received

718-P2	Endocrine and Metabolic Evaluation of Children with Neurodevelopmental Disability	giorgiana brad	Received

720-P2	Familial Williams Syndrome	Pinar Isguven	Received

721-P2	Stanazolol Abuse: Diagnostic Dilemma in an Adolescent with Persistent Hypoglycemia	Ahmet UAR	Received

722-P1	Role of the metabotropic mGlu5 glutamate receptor in the initiation of puberty and reproduction in female mice	Ioana Inta	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

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

725-P1	Metabolic and Pubertal Alterations in Children with Narcolepsy-Cataplexy.	carine villanueva	Received

726-P1	TIME COURSE OF CENTRAL PRECOCIOUS PUBERTY DEVELOPMENT CAUSED BY AN MKRN3 GENE MUTATION: A PRISMATIC CASE	Monica Stecchini	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

728-P1	FGFR1 loss-of-function mutations of in three Japanese patients with isolated hypogonadotropic hypogonadism and split hand/foot malformation	Kohnosuke Ohtaka	Received

729-P1	Clinical and mutational spectrum in Slovenian patients with hypogonadotropic hypogonadism	Magdalena Avbelj Stefanija	Received

730-P1	MKRN3 mutations and Central Precocious Puberty	Meropi Toumba	Received

731-P1	PRECOCIOUS PUBERTY IN PATIENTS WITH PRIMARY ADRENAL INSUFFICIENCY DUE TO MELANOCORTIN RECEPTOR 2 MUTATION	Firdevs Bas	Received

732-P1	Association between estrogen receptor gene polymorphisms and premature thelarche	Jong Seo Yoon	Received

733-P1	The influences of circulating leptin, kisspeptin, and neurokinin B levels to precocious puberty in obese girls	Min Jae Kang	Received

734-P1	Pseudopuberty in a young girl with Adrenocortical Carcinoma during Mitotane therapy.	Romana Marini	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

736-P1	Cut-off values for nocturnal salivary testosterone to enable detection of early puberty	Linda van der Sande	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

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

740-P1	STANDARD TRIPTORELIN THERAPY MAY NOT FULLY SUPPRESS PUBERTAL PROGRESS IN ADOLESCENTS WITH GENDER DYSPHORIA	Gary Butler	Received

741-P1	Serum anti-mullerian hormone levels in precocious puberty girls according to the timing of GnRH agonist treatment	Hyo-Kyoung Nam	Received

742-P1	PRECOCIOUS PUBERTY IN SEPTO-OPTIC DYSPLASIA SYNDROME PRESENTATION OF 2 CASES.	Elzbieta Marczak	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

744-P1	A Prospective Evaluation Of Urinary Gonadotrophins For Assessment And Management Of Pubertal Disorders	Laura Lucaccioni	Received

745-P1	Constitutional delay of puberty or hypogonadotropic hypogonadism: diagnostic value of inhibin B and AMH measurements.	Sibel Istanbullu	Received

746-P1	Prognostic significance of the proliferative index Ki67 for patients with craniopharyngiomas.	El&380;bieta Moszczy&324;ska	Received

747-P1	Etiology, differential diagnosis and clinical course of delayed puberty: a single center experience	Tero Varimo	Received

748-P1	GH therapy assessment in GH deficient patients during the transition period	Amina BOUNAGA	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

751-P1	Transcriptional Basis of Idiopathic Central Hypogonadism in Isolated Congenital Cryptorchidism with Defective Mini-Puberty	Faruk Hadziselimovic	Received

752-P1	A novel MKRN3 frameshift mutation in a Bulgarian girl with central precocious puberty	Mihaela Dimitrova-Mladenova	Received

753-P1	The intra- and inter-user reliability of Testicular Volume estimation a simulation study.	Ladan Akbarian-Tefaghi	Received

754-P1	The metabolic negative effect of gonadotropin-releasing hormone agonist therapy in childhood: is it short-term and reversible?	Barbara Predieri	Received

756-P1	-hCG from an occult source causing Peripheral Precocious puberty: identification of the tumour 6 years after presentation	Azad Ekberzade	Received

757-P1	Silent corticotroph adenoma with adrenocortical choristoma in an 11-years old boy	Oya Ercan	Received

758-P2	Clinical symptoms, Endocrine dysfunction and Radiologic findings in children with Rathkes Cleft cyst	Jo Eun Jung	Received

759-P2	A CASE OF CENTRAL PRECOCIOUS PUBERTY IN A PATIENT WITH PRADER-WILLI SYNDROME	Maria Chiara Pellegrin	Received

760-P2	IS AMH LEVEL DIAGNOSTIC FOR PREMATURE TELARCHE, PREMATURE ADRENARCHE AND CENTRAL PRECOCIOUS PUBERTY?	Senay Savas-Erdeve	Received

761-P2	Paediatric Cushing Disease: one patients path to cure	Galina Yordanova	Received

762-P2	Recovery of hypothalamic pituitary function after stalk transection and panhypopituitarism in an adolescent	margaret Zacharin	Received

763-P2	A novel CHD7 mutation in an adolescent presenting with pubertal and growth delay	MARIA-CHRISTINA ANTONIOU	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

765-P2	Symptomatic Rathke cleft cyst in pediatric patients - clinical presentations, surgical treatment and postoperative outcomes - an analysis of 38 cases	Monika Prokop	Received

766-P2	Congenital craniopharyngioma: report of two cases	Agnieszka Bogusz	Received

767-P2	Congenital hypopituitarism in a patient with 18p- syndrome	Anna Bolmasova	Received

768-P2	10 years review of endocrine diseases in Spanish patients diagnosed with primary brain tumors in a tertiary hospital.	Rica Itxaso	Received

769-P2	Novel uses of psychiatric drugs to treat hypothalamic obesity	Maria Cristina Azcona	Received

770-P2	POSTOPERATIVE WATER AND ELECTROLYTE DISORDERS AND AFFECTING FACTORS IN CHILDREN WITH INTRACRANIAL TUMORS	esra doger	Received

771-P2	Compound heterozygosity for two novel POU1F1 mutations in siblings with isolated childhood onset Growth Hormone Deficiency (CO-GHD)	Mariana Grace	Received

772-P2	Brain MRI in evaluation of endocrine diseases of childhood : causal and incidental lesions	Emilie SELBONNE	Received

773-P2	Primary thirst defect is a rare but important complication following surgery for hypothalamic hamartoma and intractable epilepsy	Giri Dinesh	Received

774-P2	Insulin Sensitivity in Girls with Central Precocious Puberty at Diagnosis and at 6 Months of GnRH Analogue Treatment	Andrea Arcari	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

776-P2	Central nervous system abnormalities on brain magnetic resonance imaging among 200 Korean Girls with central precocious puberty	Shin-Hee Kim	Received

777-P2	Impaired growth hormone secretion associated with large hypothalamic hamartoma	Elena Sukarova-Angelovska	Received

778-P2	Comparison of triptorelin versus leuprolide in treatment of girls with central precocious puberty	Glay Can Yilmaz	Received

779-P2	Central precocious puberty in a female with gonadal dysgenesis and bilateral gonadoblastoma	Stefano Stagi	Received

780-P2	Precocious puberty: a single academic center experience	Heta Huttunen	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

782-P2	EARLY PUBERTY; DIAGNOSIS, TREATMENT AND PROGNOSIS	esra doger	Received

783-P2	BASAL LEVELS OF FSH AND LH CAN BE HELPFULL IN DIAGNOSIS OF PUBERTY PRECOCIOUS?	Ulku Gul	Received

784-P2	Body Mass Index and Body Fat Composition are Both Related to Central Precocious Puberty in Chinese Girls	Ke Huang	Received

785-P2	HYPERLEPTINEMIA IN OBESE AND NON-OBESE CHILDREN WITH EARLY PUBERTY	KYUNG-MI JANG	Received

786-P2	Association between Congenital Hypopituitarism and Agenesis of the Internal Carotid Artery: a case report.	Alessandra Cocca	Received

787-P2	Giant macroprolactinoma in a female adolescent - case report	Ana Hreniuc	Received

788-P2	ADENOMAS PITUITARY IN CHILDREN	soumeya fedala	Received

789-P2	A Patient With Multiple Endocrine Neoplasia Type 1 Presented With Precocious Puberty	Nese Akcan	Received

790-P2	PRECOCIOUS PUBERTY IN A GIRL WITH PRADER WILLI SYNDROME (PWS)	MARIA PAPAGIANNI	Received

791-P2	MENSTRUAL CHARACTERISTICS AND PROBLEMS IN 918 YEARS OLD TURKISH SCHOOL GIRLS	Mustafa Kendirci	Received

792-P2	Haplo-insufficiency for LHX4 alone does not result in hypopituitarism.	Evelien Gevers	Received

793-P2	A Nursing Perspective: Best practices for pubertal suppression for individuals with central precocious puberty and transgender	Eileen Pyra	Received

794-P2	An unusual association between empty sella and central precocious puberty	Stefano Stagi	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

796-P2	Severe Juvenile Hypertrophy of the Breast with hypercalcaemia; mastectomy vs reduction surgery	David McGregor	Received

797-P2	Report two cases of dopa-responsive dystonia.	zhuannan Jiang	Received

799-P1	NPR2 gene mutations associated with acromesomelic dysplasia Maroteaux type are mostly unique to families	Lidia Castro-Feijoo	Received

800-P1	Rare cases of ornithine transcarbamylase deficiency and variant Turner syndrome	Yoo-Mi Kim	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

802-P1	COGNITIVE EVALUATION IN SILVER RUSSELL CHILDREN	GIUSEPPA PATTI	Received

803-P1	Body Surface Area Estimation In Girls With Turner Syndrome:Implications For Interpretation Of Aortic Sized Index	Sze Choong Wong	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

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

806-P1	Metabolic Health and Long-term Safety of GH-Treatment in Silver-Russell Syndrome	Carolina Smeets	Received

807-P1	Auxological features in patients with Juvenile Idiopathic Arthritis (JIA) treated with biologic therapy preliminary study data	Stefano Stagi	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

809-P1	Early treatment with rhGH in patients with Prader-Willi syndrome results in improved height with no respiratory adverse effects.	Kyriaki Alatzoglou	Received

810-P1	Phenotypic variability in a family with a new SHOX gene mutation	Adalgisa Festa	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

812-P1	Skeletal Disproportion In Girls With Turner Syndrome	Sze Choong Wong	Received

813-P1	Reconsideration of mid-parental height calculation	Serap Turan	Received

814-P1	Altered Thyroid function following Growth Hormone (GH) Initiation in children with Prader-Willi syndrome (PWS)	Musthaffa Yassmin	Received

815-P1	6-year-old girl with mutation in DNMT3A a new overgrowth syndrome.	Ann-Margrethe Rnholt	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

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

818-P1	Haploinsufficiency of short stature homeobox containing gene (SHOX): clinical signs and anthropometric measurements in children.	Alice Monzani	Received

819-P1	Clinical and molecular characterization of a newly recognized overgrowth syndrome: interstitial 7q22.1-7q22.3 microdeletion	Chong Kun Cheon	Received

820-P1	INTERNATIONAL COOPERATIVE GROWTH STUDY, NutropinAq European Registry (iNCGS): Countries specificities	Nick Brown	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

822-P1	Neonatal haematological complication in Noonan syndrome future concerns about growth hormone therapy	Laura Kasongo	Received

823-P1	Effects of a Stressful Environment (SE) on Height, BMI and Menarche	Alina German	Received

824-P1	GROWTH HORMONE DEFICIENCY IN NOONAN SYNDROME: DOES IT INFLUENCE CLINICAL RESPONSE TO GH THERAPY?	Maria Chiara Pellegrin	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

826-P1	Etiologic distribution and characteristics of patients with short stature in a Pediatric Endocrinology Clinic	Saygin Abali	Received

827-P1	OSBPL5 methylation abnormalities may be pathogenic in Silver Russell syndrome through genomic methylation analysis	DI WU	Received

828-P1	A study of Bone Health Index (BHI) in girls with Turners Syndrome	Joanne Blair	Received

829-P1	Premature adrenarche in Silver-Russell syndrome: a longitudinal study	Nawfel Ferrand	Received

830-P1	A RARE CASE OF DELETION IN 2q24.1: CLINICAL FEATURES AND RESPONSE TO GH HORMONE TREATMENT	Maria Cristina Maggio	Received

832-P1	Effect of dietetic management on weight in children with Bardet-Biedl Syndrome	Suma Uday	Received

834-P2	Auxological Features in Patients with Vernal Keratoconjunctivitis	Stefano Stagi	Received

835-P2	Turner Syndrome: does GH treatment influence glucose homeostasis?	Federico Baronio	Received

836-P2	Renal anomalies in children with Turner Syndrome: experience from a single-centre	Laura Lucaccioni	Received

838-P2	A novel fibrillin-1 gene mutation leading to Marfan syndrome in Korean girl	Hyo-Kyoung Nam	Received

839-P2	Evaluation of Referrals for Short Stature to a Regional Paediatric Centre	David Yue	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

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

842-P2	Linear Growth in Infants and Children with Atopic Dermatitis.	Ashraf Soliman	Received

843-P2	The specific pubertal height gain is higher in boys as well as in children with lower BMISDS	Anton Holmgren	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

845-P2	THE 3M SYNDROME: A CAUSE OF PRE- AND POST-NATAL SEVERE GROWTH RETARDATION	Firdevs Bas	Received

846-P2	Should we construct specific growth charts for ethnic subgroups?	Pop Raluca-Monica	Received

847-P2	Late presenting girls with Turner Syndrome (TS) can achieve a normal final height.	Sophia Sakka	Received

848-P2	GROWTH OF CHILDREN BORN PRETERM DURING THE FIRST 8 YEARS OF LIFE	Adriane Cardoso-Demartini	Received

849-P2	Genetic variability in patients with Noonan syndrome in the Republic of Macedonia	Mirjana Kocova	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

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

852-P2	Assessment of the medical and psychological status of women with Turner-Syndrome in young adulthood	Diana-Alexandra Ertl	Received

853-P2	A 3-year-old boy with growth hormone deficiency and clinical features of Ritscher-Schinzel syndrome	Sonya Galcheva	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

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

856-P2	A RARE CAUSE OF SHORT STATURE: PATIENT WITH 3M SYNDROME REVEALED A NEW MUTATION IN OSBL1 GENE	Meliksah Keskin	Received

857-P2	A case of familial Silver-Russell syndrome	Julia Hoppmann	Received

858-P2	Central precocious puberty in a case of SOTOS syndrome	Sharon Lim	Received

860-P2	Referral Pattern of Children with Short Stature to a Pediatric Endocrine Clinic in Kuwait	Al-Abdulrazzaq Dalia	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

862-P2	Dopamine Beta-Hydroxylase Deficiency Leading to Growth Hormone Deficiency	Hakan Dneray	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

865-P2	Postnatal Growth and Factors Modifying it in Very Low Birth Weight Preterms (PT) with Bronchopulmonary Dysplasia (BPD).	Ashraf Soliman	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

867-P2	Growth Hormone treatment in a child with Trisomy 21 and Turner Mosaicism	Sharon Lim	Received

868-P2	Pubertal development and Final Height in some rare genetic diseases.	LAURA MAZZANTI	Received

869-P2	Growth hormone deficiency in a patient with ring chromosome 18	Maria Korpal-Szczyrska	Received

870-P2	Children with Down syndrome show quantitative, phenotypical and functional differences of effector T-cells compared to immunocompetent controls	Justine Schoch	Received

871-P2	CARDIOVASCULAR ANOMALIES IN TURNER SYNDROME	soumeya fedala	Received

872-P2	Metamemory in Turner syndrome: a study comparing episodic and semantic memory	Céline Souchay	Received

873-P2	A XO/XX girl with lack of morphological UTS-features, short stature and precocious puberty	Birgit Vogel	Received

874-P2	Transverse Myelitis in Turner Syndrome	Cristiane Kopacek	Received

875-P2	Tricho-Rhino-Phalangeal Syndrome Type I in a girl with Growth Hormone Deficiency	Meltem Didem Cakir	Received

877-P2	Pituitary gigantism and central precocious puberty presenting with prognathism in a pediatric patient	Carla Minutti	Received

878-P2	The monitoring of endocrine functions in children with rare genetic syndromes	Natallia Akulevich	Received

880-P2	Late diagnosis of mixed gonadal dysgenesis - clinical and psychological implications	Mirela Puiu	Received

881-P2	The structure of genetically determined types of short stature in Uzbekistan according to retrospective analysis	Nilufar Ibragimova	Received

882-P2	EVALUATION OF GROWTH PATTERN IN PRADER-WILLI SYNDROME	Sevinc Odabasi Gunes	Received

883-P2	Prader-Willi Syndromedifferent patients, different attitude	Anamaria Bursuc	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

885-P1	Elevation of serum fibroblast growth factor 21 in congenital hypothyroidism	Shuichi Yatsuga	Received

886-P1	Evaluation of Epicardial Adipose Tissue Thickness in Children Detected Subclinical Hypothyroidism	Ayca Torel Ergur	Received

887-P1	EEG alterations are common in Hashimotos Thyroiditis	Claudia Boettcher	Received

888-P1	Semi-hot thyroid nodules associated with GNAS mutations in three adolescents	ANNE-SPOHIE LAMBERT	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

890-P1	The molecular causes of congenital hypothyroidism: The Scottish experience	mariam kourime	Received

891-P1	Newborn Screening Program for Congenital Hypothyroidism: eighteen years of experience in Buenos Aires Province, Argentina.	Verónica González	Received

892-P1	Transient TSH elevation in infants referred on newborn screening features, prevalence and trends	Yasmine Ouarezki	Received

893-P1	Resolution of hepatic hemangiomas and consumptive hypothyroidism in an infant treated with propranolol and levothyroxine	Victoria Campbell	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

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

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

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

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

899-P1	Clinical And Histopathologic Features And Follow-Up Of Paediatric Patients With Papillary Thyroid Cancer: A 10 Years Experience.	ROBERTO ZUART	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

901-P1	Screening of congenital hypothyroidism in low birth weight and very low birth weight neonates: A systematic review	Mahin Hashemipour	Received

902-P1	Identification of zinc transporter ZnT8 in thyroid tissues from children and adolescents with thyroid nodular hyperplasia	Artur Bossowski	Received

903-P1	HABP2 as genetic susceptibility factor for Familial Differentiated Thyroid Carcinoma.	Rajdee de Randamie	Received

904-P1	Cardiac size and function in children with subclinical hypothyroidism	Sara Alfano	Received

905-P1	Association of CTLA4, PADI4 and FTO polymorphisms with autoimmune thyroid diseases in male children.	Aleskandra Goralczyk	Received

906-P1	Thyroid cancers in Korean pediatric populations with thyroid nodules	SO HYUN PARK	Received

907-P1	Dysregulation of the immune system in children with Graves disease the role of NK and NKT-like cells	Maria Klatka	Received

908-P1	Thyroid function anomalies in children with Down syndrome: early TSH alteration can predict future hypothyroidism development?	Giorgio Ottaviano	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

911-P1	Hyperthyroidism after Bone Marrow Transplantation: A Report of Two Cases	Hiroyuki Ishiguro	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

913-P1	Nerve Conduction Studies in Children with Subclinical Hypothyroidism	Gonul Catli	Received

915-P1	Macro TSH- a Rare Cause of High Levels of TSH	Selin Elmaogullari	Received

916-P1	Papillary thyroid carcinoma in a mother and child after manifestation of Graves disease	Erwin Lankes	Received

917-P1	Hypercholesterolemia in two siblings with THRB mutation	Urh Groselj	Received

918-P1	Thyroid Autoimmunity and Vitamin D Status in Euthyroid Girls with Hashimotos Thyroiditis	Pinar Isguven	Received

919-P1	Etiology and severity of congenital hypothyroid children detected through neonatal screening: a cut-off based analysis	Ana Vieites	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

921-P1	Differentiated thyroid cancer: onset and outcome in a pediatric population with and without risk factors	Federico Baronio	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

923-P1	Small thyroid volume on ultrasound in infants with transient TSH elevation following referral by newborn screening	Chourouk Mansour	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

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

926-P1	Minimally invasive video-assisted thyroid surgery (MIVAT) in children: a single center ten-years experience	graziamaria ubertini	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

928-P1	PRELIMINARY RESULTS: BODY COMPOSITION OF ADOLESCENT PATIENTS WITH CONGENITAL HYPOTHYROIDISM AND CORRELATION WITH LABORATORY PARAMETERS	Artemis Doulgeraki	Received

929-P1	Neonatal thyrotoxicosis and craniosynostosis associated with maternal Graves disease and high dose maternal thyroxine therapy for papillary carcinoma	Sumudu Seneviratne	Received

930-P1	Seasonality of month of birth in children and adolescents with Hashimoto thyroiditis	Ioannis Kyrgios	Received

931-P1	Radioiodine therapy for Graves disease the experience of a Portuguese single centre	Nuno Vicente	Received

932-P2	MULTINODULAR GOITER AND DIFFERENTIATED THYROID CANCER IN PEDIATRICS	Patricia Papendieck	Received

933-P2	Clinical case of acute liver injury in pediatric patient with autoimmune hyperthyroidism	MARIA CRISTINA VIGONE	Received

934-P2	Thyroid function in children affected by Congenital Hypothyroidism (CH) with eutopic thyroid after discontinuation of treatment with Levothyroxine	ROBERTO GASTALDI	Received

935-P2	HYPERTHYROIDISM IN AN INFANT OF A MOTHER WITH AUTOIMMUNE HYPOTHYROIDISM WITH POSITIVE TSH RECEPTOR ANTIBODIES	margaret zacharin	Received

936-P2	THYROID CANCER PRESENTATION IN CHILDREN IS DIFFERENT THAN IN YOUNG ADULTS	Malgorzata Wasniewska	Received

937-P2	Starting treatment in congenital hypothyroidism with normal FT4 levels and thyroid gland in situ detected at neonatal screening	Laura Paone	Received

938-P2	Distal monosomy 10q presented as congenital hypothyroidism	Elena Emanuela Braha	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

940-P2	An unusual case of impaired renal function and thrombocytopenia	Luminita Nicoleta Cima	Received

941-P2	Celiac Disease in Children and Adolescents with Hashimoto Thyroiditis	Hale Tuhan	Received

942-P2	Euthyroid Hashimoto thyroiditis in children : evolution over time	FENELI KARACHALIOU	Received

943-P2	Thyrotoxic Periodic Paralysis, an under-recognized condition	Carolina Di Blasi	Received

944-P2	Age at diagnosis and mental development in children with congenital hypothyroidism in the absence of newborn screening programme.	Yasmine Ouarezki	Received

946-P2	The clinical predictive factors for differentiation transient congenital hypothroidism from congenital hypothyroidsm patients	Se Young Kim	Received

947-P2	Delayed Diagnosis of a TSH-adenoma Due to Coexisting Autoimmune Thyroid Disease	David Crudo	Received

948-P2	Kocher-Debre-Semelaigne syndrome: hypothyroidism with muscle pseudohypertrophy.	Elena Bogova	Received

949-P2	Thyroid function in obese children and its correlations with chosen atherogenic risk factors	Beata Pyrzak	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

951-P2	Hashimotos Thyroiditis in childhood: an 8 year experience	SOTIRIA GIANNOPOULOU	Received

952-P2	Congenital Malformations, Dysmorphic Syndromes and Neurodevelopmental Problems in Children with Congenital Hypothyroidism	Voutetakis Antonis	Received

953-P2	Clinical value of thyroid-stimulating immunoglobulin in paediatric autoimmune thyroid diseases	Karolina Stozek	Received

954-P2	Hearing, language and communication abilities in children with congenital hypothyroidism	Hannah Cooper	Received

955-P2	Lack of catch up growth in young children with severe Hashimoto thyroiditis	Audrey VINCENT	Received

956-P2	Perinatal factors associated with neonatal thyroid stimulating hormone in normal newborns	Seong Yong Lee	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

959-P2	Thyroid hormones and risk factors in obese and overweight children	SOTIRIA GIANNOPOULOU	Received

960-P2	FNA: a gold standard in the diagnosis of thyroid nodules in children after chemotherapy	SOFIA LEKA	Received

961-P2	Profound growth failure in peripubertal adolescents presenting with severe acquired autoimmune hypothyroidism a case series	Swathi Upadrasta	Received

962-P2	TWO PATIENTS WITH RESISTANCE TO THYROID HORMONES	ESRA DENIZ PAPATYA CAKIR	Received

963-P2	The influence of etiology and treatment factors on intellectual outcome in congenital hypothyroidism	Jong Seo Yoon	Received

964-P2	An unusual complication of Graves disease.	Akintayo Adesokan	Received

965-P2	An unusual form of precocious puberty: Van Wyk and Grumbach syndrome	AHMET ANIK	Received

966-P2	Clinical Features of Newborn with Congenital Hypothyroidism Diagnosed by Neonatal Screening: Single Center Experience	AYLA GUVEN	Received

967-P2	Postoperative complications of thyroidectomy in children with nodular goiter	Olga Rogova	Received

969-P2	An unusual presentation of Hashimoto thyroiditis (HT) and precocious puberty: The VAN WYK-GRUMBACH Syndrome	SOFIA LEKA	Received

970-P2	Rare Case of Severe Hyperthyroidism due to Graves Disease in a Toddler	Parissa Salemi	Received

971-P2	Youngest Known Case of Autoimmune Thyroiditis Causing Hyperthyroidism in a Downs Syndrome Toddler	Parissa Salemi	Received

972-P2	Thyroid hormones in obese children	SOTIRIA GIANNOPOULOU	Received

973-P2	A case of neonatal Graves in a premature infant with negative thyrotropin receptor stimulating antibodies	Carla Minutti	Received

974-P2	Severe growth retardation and hypothyroidism due to Hashimotos thyroidits	Marina Krstevska-Konstantinova	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

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

977-P2	Very early onset of autoimmune thyroiditis in a toddler with multi-organ involvement	Giuseppina Rosaria Umano	Received

978-P2	The case of the thyroid gland dystopia in the root of the tongue	Svitlana Chumak	Received

979-P2	A case report:Conversion of autoimmune hypothyroidism to hyperthyroidism in A child with Downs syndrome.	abdullah alshahrany	Received

980-P2	Transient congenital hypothyroidism: About 6 cases	soumeya fedala	Received

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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