EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY
53rd Annual ESPE Meeting 201418-20 September 2014 DUBLIN
N. Poster
Poster title
Applicant name
Status
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| 621-P3-D1 | The effect of working in a childrens hospital on urinary catecholamine excretion rates in male and female physicians | Claudia Boettcher |  Received |
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| 622-P3-D1 | Body Composition Analysis in Girls with Premature Adrenarche | Ayse Nurcan Cebeci | Received |
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| 623-P3-D1 | PseudoHypoAldosteronism Type 1 (PHA1): role of urinary steroid profiling (USP) in specific and early diagnosis lessons in differential diagnosis of PHA1 vs PHA2 (renal tract anomaly) | Vimmi Abbot | Received |
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| 627-P3-D1 | A Rare Cause of Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency: A Case Report | peyami cinaz | Received |
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| 629-P3-D1 | Clinical and genetic diagnosis of Allgrove syndrome | Zdravka Todorova | Received |
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| 630-P3-D1 | Clinical case of Cushing syndrome in secreting NET | GIANLUCA MUSOLINO | Received |
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| 632-P3-D1 | Secondary Pseudohypoaldosteronism Type 1 the role of a Urinary Steroid Profile in diagnosis. | Mariana Grace | Received |
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| 633-P3-D1 | Steroid 11Hydroxylase deficiency in Egyptian children | Noha Musa | Received |
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| 634-P3-D2 | PRENATAL DEXAMETHASONE USE FOR THE PREVENTION OF VIRILIZATION IN PREGNANCY AT RISK FOR CLASSICAL CONGENITAL ADRENAL HYPERPLASIA | María Sanz Fernández | Received |
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| 635-P3-D2 | Congenital Adrenal Hyperplasia- Survey of the management in children across U.K | Usha Niranjan | Received |
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| 636-P3-D2 | Neonatal hpercalcaemia associated with congenital adrenal hyperplasia | Cigdem Binay | Received |
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| 639-P3-D2 | Four Cases of Ovarian Adrenal Rest Tumors in Chinese Girls with Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency. | ZHE SU | Received |
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| 640-P3-D2 | Therapeutic troubles of Cushings disease in adolescence: report of a case | MANUELA DEIANA | Received |
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| 641-P3-D2 | Congenital Hypoaldosteronism of Unknown Etiology in Five Half-Siblings | Jan Foote | Received |
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| 642-P3-D2 | X-linked adrenoleukodystrophy in 8 patients. | Zhe Meng | Received |
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| 644-P3-D2 | Cushing Syndrome without origin | Sara Queirolo | Received |
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| 645-P3-D2 | Untreated congenital adrenal hyperplasia with central precocious puberty | Mihaela Dimitrova | Received |
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| 646-P3-D3 | Hypothyroidism in anorexia nervosa due to primary autoimmune pathogenesis | Rajesh Chidanandaswamy | Received |
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| 647-P3-D3 | Autoimmune disease and Arnold Chiari Syndrome: any correlation? | Elvira Piccinno | Received |
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| 648-P3-D3 | Genetically proven APS type 1 in two siblings | Desislava Yordanova | Received |
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| 649-P3-D3 | Rare association of diabetes insipidus and autoimmune thyroiditis in 11-year-old girl | Mirjana Kocova | Received |
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| 651-P3-D3 | Diabetes mellitus after hematopoietic stem cell transplantation | karla maria narvaez barros | Received |
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| 652-P3-D3 | PRESERVATION OF OVARIAN FUNCTION IN YOUNG FEMALES CANCER SURVIVORS WITH RISK OF OVARIAN FAILURE | Maria J. Chueca Guindulain | Received |
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| 653-P3-D3 | Late endocrine effects in children and adolescentes submitted to allogenic bona marrow tranplantation | HILTON KUPERMAN | Received |
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| 654-P3-D3 | Adrenocortical tumor: a case report | Elisa Guidoni | Received |
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| 655-P3-D3 | A conservative approach to the management of endocrine neoplasia in Carney Complex in an adolescent male | Carley Frerichs | Received |
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| 658-P3-D3 | Increasing Testicular Size Due to Bilateral Large Cell Calcifying Sertoli Cell Tumours (LCCSTs) in a peri-pubertal child with Carney Complex | Sarah Geoghegan | Received |
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| 663-P3-D1 | HYPOVITAMINOSIS D: FACTORS AFFECTING IN SPANISH CHILDREN AND ADOLESCENTS | Maria Rosaura Leis | Received |
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| 665-P3-D1 | Survey of vitamin D status in breastfeeding infants under the age of 6 months attending the growth monitoring clinic at Rubaga hospital. | Cissy Nalunkuma | Received |
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| 666-P3-D1 | Hypercalciuria in Patients with Coexisting Osteogenesis Imperfecta and Renal Tubular Acidosis | Luisa Aguiar | Received |
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| 667-P3-D1 | METABOLIC AND BONE DISORDERS IN VERTICALLY HIV-INFECTED CHILDREN | maritza vivanco | Received |
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| 670-P3-D1 | Primary hypomagnesaemia with secondary hypocalcaemia (HSH) : An uncommon diagnosis for a 2 month old Afro-Caribbean formula fed infant presenting with seizures. | Ihe Chibuzor | Received |
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| 671-P3-D1 | A Challenging Diagnosis of Pseudohypoparathyroidism type 1a and practical management: a case report | Mariana Grace | Received |
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| 675-P3-D2 | FGFR3 GENE: A VERY RARE MUTATION | María Magdalena Hawkins | Received |
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| 677-P3-D2 | Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets | Melik&351;ah Keskin | Received |
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| 678-P3-D2 | When is epilepsy not epilepsy | Richard Lloyd-Nash | Received |
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| 679-P3-D2 | Evaluation of Patients with Stunting in Armenia | Renata Markosyan | Received |
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| 680-P3-D2 | Fluctuation in cerebral calcification in a patient with pseudohypoparathyroidism type II | Elena Sukarova-Angelovska | Received |
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| 681-P3-D2 | VARIABILITY IN CLINICAL AND GENETIC SPECTRUM IN HYPOPHOSPHATASIA: NATURAL HISTORY IN TWO PATIENTS | Gabriel Á. Martos-Moreno | Received |
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| 682-P3-D2 | Cautionary Tales in the Management of Transient Neonatal Hypoparathyroidism | Ian Mulvey | Received |
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| 684-P3-D2 | Clinical phenotype and molecular studies in patients with hypophosphatemic rickets | Monika Obara-Moszynska | Received |
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| 685-P3-D2 | Autosomal-dominant hypocalcaemia, new clinical features | Noemi Fuentes-Bolaños | Received |
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| 686-P3-D3 | Bone Health in a cohort of Irish Spinal Muscular Atrophy (SMA) Patients | Niamh Mc Sweeney | Received |
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| 686-P3-D2 | Intravenous Zoledronic Acid: Experience of Treatment of Children with Osteogenesis Imperfecta in Indonesia | Dwi Lestari Pramesti | Received |
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| 687-P3-D3 | Endocrinological assessment of children with bronchiectasis | Ilker Tolga Ozgen | Received |
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| 688-P3-D3 | Mutational analysis of TAC and TAC3 in idiopathic central precocious puberty | Marina Krstevska-Konstantinova | Received |
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| 689-P3-D3 | Vitamin D levels in short prepubertal children born small for gestational age (SGA) | Maria Korpal-Szczyrska | Received |
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| 690-P3-D3 | Prospective evaluation of bone mineralization, PTH regulation and metabolic profile in adult patients with hereditary hypophosphatemic rickets. | emese boros | Received |
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| 691-P3-D3 | Bone mineral density and vitamine D status in girls and adolescents with Turner Syndrome: | BAZ OUIDAD | Received |
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| 693-P3-D3 | THE USE OF PAMIDRONATE IN PEDIATRIC PATIENTS WITH DISEASE OF OTHER THAN OSTEOGENESIS IMPERFECTA: THE EXPERIENCE OF OUR CENTER | Ayla Gven | Received |
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| 694-P3-D3 | McCune-Albright Syndrome associated to hypophosphatemic rickets | TIAGO JERONIMO DOS SANTOS | Received |
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| 696-P3-D3 | A Korean boy with pseudohypoparathyrodism type Ia presenting with congenital megacolon and spinal stenosis : Identification of a novel GNAS gene mutation | Ji Eun Lee | Received |
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| 697-P3-D3 | A CASE WITH ODONTOHYPOPHOSPHATASIA AND FAMILY INVESTIGATION | Esra Deniz Papatya Cak&305;r | Received |
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| 698-P3-D3 | TSH/fT4 ratio as a marker of TSH resistance in Pseudoparathyroidism 1A and obesity | Aurélia Alimi | Received |
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| 699-P3-D3 | Infantile hypophosphatasia | Nevenka Slaveska | Received |
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| 699-P3-D1 | Efficacy and safety of CSII treatment in paediatric age. Long term experience of a tertiary care centre in Spain. | Esmeralda Colino | Received |
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| 701-P3-D1 | Changing Presentation of Type 1 Diabetes to a Tertiary Paediatric Centre | Niamh Mc Grath | Received |
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| 703-P3-D1 | Urinary C-Peptid/Creatinine Ratio in Children and Adolescents Diagnosed withMaturity-Onset Diabetes of the Young (MODY) | Sebahat Yilmaz Agladioglu | Received |
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| 704-P3-D1 | A case with neonatal diabetes and congenital hypothyroidism due to GLIS3 gene deletion | Ilker Tolga Ozgen | Received |
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| 705-P3-D1 | Glycemic control of patients with type 1 Diabetes using automated bolus calculator glucometer | Jaime Cruz Rojo | Received |
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| 708-P3-D1 | Clinical significance of typing fulminant type 1 diabetes in children and adolescents | wang yi | Received |
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| 709-P3-D1 | Continuous Subcutaneous Insulin Infusion Therapy in Preschool Children with Type 1 Diabetes Mellitus | Rita Moinho | Received |
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| 712-P3-D2 | Audit of the use of integrated care pathway in the management of Diabetic keto acidosis in children | Ravi Palakurthi | Received |
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| 713-P3-D2 | Development of diabetes mellitus after hematopoietic stem cell transplantation for childhood leukemia | In Ah Jung | Received |
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| 714-P3-D2 | Case of family neonatal diabetes with KCNJ11 gene mutation | Svitlana Chumak | Received |
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| 716-P3-D2 | Uptake of a novel tool to adjust insulin boluses, based on CGM trend arrows and insulin sensitivity (Trend Arrow Adjustment Tool); in children with type 1 diabetes, who are using insulin pump therapy and continuous glucose monitoring. | Emmeline Heffernan | Received |
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| 718-P3-D2 | INCIDENCE OF DIABETES MELLITUS AND ASSOCIATED COMPLICATIONS AMONG CHILDREN: RESULTS FROM AZERBAIJAN DIABETES REGISTRY 1997-2007 | Gunduz Ahmadov | Received |
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| 719-P3-D2 | Arabic Translation and Validation of the Newest Vital Sign Health Literacy Tool: A Pilot Project to Test Health Literacy of Caregivers of Children with Type 1 Diabetes in Kuwait | Dalia Al-Abdulrazzaq | Received |
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| 720-P3-D2 | ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODIES ARE NOT FREQUENT IN CHILDREN WITH TYPE 1 DIABETES | Melek Y&305;ld&305;z | Received |
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| 721-P3-D2 | GLYCEMIC VARIABILITY AND METABOLIC CONTROL IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES MELLITUS | María Martín-Frías | Received |
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| 722-P3-D2 | Knowledge base and attitudes of senior medical staff to insulin therapy in children with diabetes | Amith Nuti | Received |
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| 724-P3-D3 | Prevalence of impaired glucose tolerance and insulin resistance in a sample of the 6- to 16-year-old overweight or obese pediatric population | Fatemeh Saffari | Received |
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| 725-P3-D3 | Differences in pubertal development and anthropometry between normal population and type1 diabetic child at debut in Spain | Ignacio Diez | Received |
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| 726-P3-D3 | Effect Of Vitamin D Treatment On Glucose And Insulin Metabolism, And Bone Turnover In Children With Symptomatic Vitamin D Deficiency | Nagla El Fakhri | Received |
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| 727-P3-D3 | Evaluation of HbA1c measurement in Trinidad and Tobago | Maynika Rastogi | Received |
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| 728-P3-D3 | THE RESULT OF SULPHONYLUREAS TREATMENT IN PATIENTS WITH NEONATAL DIABETES MELLITUS DUE TO KCNJ11/ABCC8 GENE MUTATIONS IN VIETNAM | Can Thi Bich Ngoc | Received |
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| 730-P3-D3 | Wolcott-Rallison Syndrome In Two Siblings With No Implication Of EIF2AK3 Mutation | AYCA ALTINCIK | Received |
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| 731-P3-D3 | Prevalence of atopic diseases in diabetic children and adolescents | Hildegard Jasser-Nitsche | Received |
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| 732-P3-D3 | The Pattern of Body Composition Change in Type 1 Diabetes by Gender | Yong Hyuk Kim | Received |
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| 733-P3-D3 | Transient Neonatal Diabetes and intermediate DEND phenotype with KCNJ11 mutation | Ana Laura Fitas | Received |
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| 735-P3-D3 | Metabolic control in a pediatric population with type 1 diabetes mellitus | Joana Verdelho Andrade | Received |
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| 736-P3-D2 | Metabolic compensation correlation with chronic complications of type 1 diabetes in children in Latvia | Zane Eglite | Received |
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| 737-P3-D2 | IGF-I levels in children with type 1 diabetes are primarily related to glycemic control and residual beta cell mass, and not affected by different modalities of insulin therapy | Carla Bizzarri | Received |
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| 738-P3-D2 | When should we suspect maturity onset diabetes of the young in children and adolescents? | Sarar Mohamed | Received |
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| 740-P3-D2 | Continuous Glucose Monitoring System (CGMS) in the Diagnosis of Early Glycemic Abnormalities in High Risk Groups | Ashraf Soliman | Received |
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| 741-P3-D2 | Incidence of dyslipidemia and its association with glycemic control in adolescents and young adults with type 1 diabetes | Min Ho jung | Received |
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| 742-P3-D2 | Learning by doing approach: use of multimedia applications in type 1 diabetic children. | Elvira Piccinno | Received |
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| 743-P3-D2 | Seip Berardinelli Syndrome Case Report | DOLY PANTOJA | Received |
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| 744-P3-D2 | 9-year old boy with Wolfram syndrome - case report | Ewa Jakubowska | Received |
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| 746-P3-D2 | CURRENT STATUS OF DIABETES MANAGEMENT , GLYCEMIC CONTROL AND COMPLICATIONS IN CHILDREN AND ADOLESCENTS WITH DIABETES: A REGISTRY-BASED STUDY IN EGYPT. WHERE DO WE STAND NOW? AND WHERE DO WE GO FROM HERE? | Nancy Elbarbary | Received |
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| 748-P3-D3 | Monogenic Diabetes in a Paediatric Population: finding the needle in the haystack. | Meenal Mavinkurve | Received |
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| 749-P3-D3 | Hyperglycemia MODY a diagnosis to remember | Ricardo Monteiro | Received |
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| 751-P3-D3 | Continuous glucose monitoring (CGMS) versus oral glucose tolerance test (OGTT) and glycated hemoglobin(HbA1C) in the evaluation of glycemic abnormalities in an obese adolescent before versus after partial gastrectomy. | Ashraf Soliman | Received |
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| 752-P3-D3 | The psychological impact of diabetes on glycaemic control in affected Saudi children at different developmental age groups | Amir Babiker | Received |
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| 753-P3-D3 | Type 1 diabetes mellitus in pediatric population: chronic complications and associated diseases | Joana Verdelho Andrade | Received |
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| 755-P3-D3 | MULTIPLE DAILY INJECTIONS SINCE THE DIAGNOSIS OF TYPE 1 DIABETES MELLITUS IN CHILDREN AND ADOLESCENTS ASSESSMENT OF 3 YEARS | RITA CARDOSO | Received |
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| 756-P3-D3 | Haemolysis and acute pancreatitis during diabetic ketoacidosis treatment in a 14-year-old boy with unknown glucose-6-phosphate dehydrogenase deficiency. | Elvira Piccinno | Received |
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| 757-P3-D3 | Pneumothorax, pneumomediastinum and subcutaneous emphysema: complications of severe DKA in T2DM obese patient. | Elvira Piccinno | Received |
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| 759-P3-D3 | Diabetes mellitus type 2 in Pediatrics : an emerging reality in our country. First cases described at Spain | Ignacio Diez | Received |
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| 760-P3-D1 | Association of Ghrelin Gene Polymorphisms with Obesity in Japanese Children | Ikuyo Itoh | Received |
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| 763-P3-D1 | Association of lifestyle with metabolic syndrome in children | Andrea Paola Rojas Gil | Received |
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| 766-P3-D1 | Positive association of pro-oxidative stress markers with adipose mass in pre- and early-pubertal boys | George Paltoglou | Received |
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| 767-P3-D1 | Prevalence metabolic syndrome and its components among children with obesity | Latyshev Oleg | Received |
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| 771-P3-D1 | Level of non-high-density-lipoprotein cholesterol and its related factors in Chinese Han students | Yanlan Fang | Received |
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| 773-P3-D2 | Trends in obesity prevalence and body-mass index among pre-pubertal Bulgarian children, 1990-2007 | violeta Iotova | Received |
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| 774-P3-D2 | The prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in Greece. | Christos Giannios | Received |
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| 775-P3-D2 | Metabolic and lifestyle correlates of health-related quality of life among Taiwanese obese adolescents | Meng-Che Tsai | Received |
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| 776-P3-D2 | Prevalence of Dyslipidemia and Associated Factors Among Obese Turkish Children | Selin Elmaogullari | Received |
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| 779-P3-D2 | Belma Haliloglu | Received |
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| 781-P3-D2 | Relationship between adiposity degree and physical activity and inactivity among children and adolescents | Maria Rosaura Leis | Received |
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| 782-P3-D2 | Antenatal and early childhood determinants of the development of obesity in children | Yauhenia Dzmitrovich | Received |
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| 783-P3-D2 | The association hypothyroidism obesity in a group of children and adolescents | Mirela Mogoi | Received |
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| 784-P3-D2 | A new lipodystrophy syndrome? | Julia von Schnurbein | Received |
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| 786-P3-D3 | Hypothalamic Obesity in Children and Adolescents: a multi-disciplinary approach and novel therapeutic tools. | DANIELE TESSARIS | Received |
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| 789-P3-D3 | Bone age advancement in prepubertal children with overweight and obesity | Hae Sang Lee | Received |
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| 790-P3-D3 | Obesity correlates in adolescence | Papandreou Ioannis | Received |
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| 793-P3-D3 | Prevalence of abnormalities of glucose metabolism in obese Greek children and adolescents | Karachaliou Feneli | Received |
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| 794-P3-D3 | PRADER WILLI SYNDROME (PWS): REPORTS OF TWO PATIENTS WITH CONGENITAL ABNORMALITIES OF KIDNEY AND URINARY TRACT. | federica tamburrino | Received |
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| 795-P3-D3 | RESPONSE TO TREATMENT IN A GROUP OF PATIENTS WITH CHILDHOOD OBESITY. | concepcion freijo martin | Received |
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| 796-P3-D3 | PREVALENCE OF OVERWEIGHT AND OBESITY IN CHILDREN AND ADOLESCENTS AT PUBLIC AND PRIVATE SCHOOLS FROM UBERABA BRAZIL | Adriana Paula Silva | Received |
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| 798-P3-D3 | Characteristics of a Population of Obese Children and Adolescents: Suggesting a new paradigm. | Quentin Van Meter | Received |
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| 799-P3-D3 | EFFECTS OF GnRH ANALOGUE TREATMENT ON INTERNAL GENITALES OF GIRLS WITH CENTRAL PRECOCIOUS | HAVVA NUR PELTEK KENDERCI | Received |
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| 801-P3-D3 | The usefulness of the Leuprolide stimulation test as a diagnostic method of idiopathic CPP in girls. | Marta Murillo Vallés | Received |
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| 803-P3-D3 | Menstrual Regularity among Early Menarche girls and CPP or EFP girls treated with GnRHa | CHEN Qiu-Li | Received |
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| 804-P3-D3 | COMPLETE BLOOD COUNT PARAMETERS IN GIRLS WITH POLYCYSTIC OVARY SYNDROME | AHMET UCAKTURK | Received |
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| 805-P3-D3 | The Genotypic and Phenotypic Variability of Mixed Gonadal Dysgenesis | Chelsey Grimbly | Received |
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| 806-P3-D3 | A rare cause for 46,XX ovarian dysgenesis: Perrault syndrome | Glay Karagzel | Received |
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| 807-P3-D3 | A rare cause of ovarian failure; ovarioleucodystrophy | Erkan Sari | Received |
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| 809-P3-D3 | THREE SIBLINGS WITH GONADAL DYSGENESIS | Fatma Dursun | Received |
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| 810-P3-D1 | The role of IGF-IR gene mutation in the development of Oligodendrocytes | Fan Yang | Received |
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| 811-P3-D1 | A Novel GHR mutation,c.4391GA;in a Family with Laron syndrome | Sameh Tawfik | Received |
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| 813-P3-D1 | Body Mass Index, IGF1-SDS and rhGH treatment | Ioannis- Anargyros Vasilakis | Received |
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| 816-P3-D1 | The level and conformation of blood plasma carotenoids in girls with Turner syndrome after 1 year of growth hormone therapy | Maria Pankratova | Received |
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| 818-P3-D1 | Assessment of compliance with Growth Hormone (GH) therapy. | Chrysoula Drosatou | Received |
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| 819-P3-D1 | Body composition in GH deficient children: effects of GH therapy and comparison between DXA and anthropometric data. | Mariacarolina Salerno | Received |
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| 821-P3-D1 | Study of Growth Hormone Receptor(GHR)exon 3 polymorphism in children with Prader-Willi Syndrome | WEI LU | Received |
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| 822-P3-D1 | Auxological evaluation of non-identical twins | Pop Raluca-Monica | Received |
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| 823-P3-D2 | Correlation between Initial Treatment Effect of Recombinant Human Growth Hormone and Exon 3 Polymorphism of Growth Hormone Receptor in Chinese Growth Hormone Deficiency Children | Zhangqian Zheng | Received |
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| 823-P3-D1 | 3-years height outcome during rh-growth hormone therapy in severe short subjects affected by skeletal dysplasias | Francesco Massart | Received |
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| 824-P3-D2 | Growth hormone deficiency in a case with Neurofibromatosis-Noonan Syndrome (NFNS) | Dogus Vuralli | Received |
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| 825-P3-D2 | Monitoring of Growth Hormone Treatment by the Electronic Auto-Injection Device easypod allows to improve the outcome and maximize adherence in patients with generally high adherence rates. | Klaus Hartmann | Received |
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| 826-P3-D2 | Usability and safety of FlexPro PenMate in patients, caregivers and healthcare professionals | Anne-Marie Kappelgaard | Received |
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| 827-P3-D2 | Impairment of glucose metabolism in Growth Hormone (GH) deficient children under GH replacement | MARIA CHATZIPSALTI | Received |
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| 828-P3-D2 | Growth response after 1 year of growth hormone (GH) treatment in children born small for gestational (SGA) without GH deficiency: our experience | gisella garbetta | Received |
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| 829-P3-D2 | CROSS- SECTIONAL AND PROSPECTIVE STUDY OF THE EFFECTS OF GH THERAPY ON METABOLIC PANEL IN CHILDREN WITH GH DEFICIENCY | Wasniewska Malgorzata | Received |
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| 830-P3-D2 | Prader Willi Syndrome and growth hormone therapy: valuable effects and adverse events | Magdalena Wilk | Received |
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| 831-P3-D2 | Recovery of central fever after GH therapy in a patient with GH deficiency secondary to posttraumatic brain injury | Hale Hale Unver Tuhan | Received |
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| 833-P3-D2 | GROWTH HORMONE TREATMENT IN 50 CHILD WITH SHORT STATURE: LEBANESE EXPERIENCE. | ABI NADER ELIE | Received |
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| 834-P3-D2 | Effectiveness of growth hormone (GH) therapy in children with short stature and decreased GH peak in stimulating tests is independent from GH secretion after falling asleep | Maciej Hilczer | Received |
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| 835-P3-D2 | An unusual case of a child with Growth Hormone Deficiency and Arnold-Chiari malformation type I. | MARIA CHATZIPSALTI | Received |
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| 836-P3-D3 | WHAT IS THE PROFIL OF GIGANTISM :7 observations | achir samia | Received |
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| 837-P3-D3 | GH treatment in Dents disease: a case report | Elisa Guidoni | Received |
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| 838-P3-D3 | ANALYSIS OF THE EFFECTIVENESS OF GROWTH HORMONE TREATMENT IN A TERTIARY HOSPITAL IN THE LAST 30 YEARS | Jaime Cruz Rojo | Received |
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| 839-P3-D3 | A Rare Syndrome Benefits From Growth Hormone Therapy: Hypotonia-Cystinuria Syndrome | Onur Akin | Received |
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| 840-P3-D3 | Changes in body mass index in GHD and SGA children in the first year of treatment | Llano Juan Pablo | Received |
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| 841-P3-D3 | Study of the effect of growth hormone treatment on growth in patients with methylmalonic acidemia. | Dirk De Weerdt | Received |
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| 843-P3-D3 | TWO YEARS OF GROWTH HORMONE THERAPY IN CHILDREN WITH GROWTH DEFICIENCY | mimouna bessahraoui | Received |
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| 844-P3-D3 | WHO growth charts replacing national reference data: Their influence on screening for over- or underweight and of growth disorders. | Dagmar l Allemand-Jander | Received |
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| 846-P3-D3 | Design and Recruitment of a Longitudinal Cohort Study of Growth and Puberty in Russian Boys | Oleg Sergeyev | Received |
|
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| 848-P3-D3 | Severe short stature with features of achondroplasia, later diagnosed as panhypopituitarism - a case report | Cristina Matei | Received |
|
|||
| 849-P3-D2 | Growth Hormone Therapy in Prepubertal Children Results after 4 years | Corina Galesanu | Received |
|
|||
| 850-P3-D2 | A follow-up Study up to adult height of the patients included in the phase III clinical trial with the Biosimilar human recombinant Growth Hormone (Omnitrope) on the treatment of Spanish children with Growth Hormone Deficit | Margarida Vasconcelos Palla Garcia | Received |
|
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| 851-P3-D2 | Growth pattern of the Nigerian child compared to International references | Chizo Agwu | Received |
|
|||
| 852-P3-D2 | Evaluation of potential waste of growth hormone across available growth hormone pen devices and an electronic growth hormone delivery device | Julie Locklear | Received |
|
|||
| 853-P3-D2 | Switching from the original to the biosimilar recombinant human Growth Hormone - Omnitrope: an experience of a single paediatric centre in Spain | Margarida Vasconcelos Palla Garcia | Received |
|
|||
| 854-P3-D2 | Descriptive Analysis of Medication Adherence for Patients Treated with Growth Hormone Therapy | Julie Locklear | Received |
|
|||
| 855-P3-D2 | EFFECT OF CONGENITAL HEART DISEASE ON PLACENTAL AND BIRTH SIZE. | Ashraf Soliman | Received |
|
|||
| 856-P3-D2 | Anthropometric evaluation of a cohort of school-aged children: the need for national growth references in Romania | Pop Raluca-Monica | Received |
|
|||
| 857-P3-D2 | Differences in personality of monozygotic twins can be predicted by difference in birth weight in teen monozygotic twins | Lioba Wimmer | Received |
|
|||
| 864-P3-D3 | The Establishment of a New Paediatric Endocrinology Training Programme in South Africa | Franois de Villiers | Received |
|
|||
| 866-P3-D3 | Growth hormone treatment adherence in children in Latvia | Zane Eglite | Received |
|
|||
| 867-P3-D3 | The effect of GH and pubertal induction therapy in Turner Syndrome. | &350;kran Darkan | Received |
|
|||
| 868-P3-D3 | Hearing loss in Turner syndrome | BAZ OUIDAD | Received |
|
|||
| 869-P3-D3 | Genotype-Phenotype Correlation in Turner Syndrome | adel djermane | Received |
|
|||
| 870-P3-D3 | Primary amenorrhea with normal stature: why not Turner syndrome? | IOANA HRISTOV | Received |
|
|||
| 871-P3-D3 | The causes of short stature in Turner syndrome | Ruimin Chen | Received |
|
|||
| 877-P3-D1 | CONGENITAL HYPERINSULINISM: CLINICAL AND MOLECULAR CHARACTERISTICS OF BRAZILIAN PATIENTS | Raphael Liberatore Junior | Received |
|
|||
| 879-P3-D1 | Congenital Hyperinsulinism: A Single-Center Experience | Murat Dogan | Received |
|
|||
| 880-P3-D1 | Persistent hyperinsulinemic hypoglycemia of an infancy carrying ABCC8 Arg598stop mutation | Jianfang Zhu | Received |
|
|||
| 881-P3-D1 | A Case of Hyperinsulinism/hyperammonemia Syndrome. | Young Suk Shim | Received |
|
|||
| 882-P3-D1 | PROJECT epiSGA - PreMeb . Presentation , subject recruitment and initial data | Ignacio Diez | Received |
|
|||
| 885-P3-D1 | Neonatal seizures neonatal due to hypocalcemia secondary to maternal vitamin D deficiency | ARIADNA CAMPOS MARTORELL | Received |
|
|||
| 888-P3-D2 | Neonatal Neurogenic Diabetes Insipidus a case report | INS ALVES | Received |
|
|||
| 889-P3-D2 | Evolution and epidemiological assessment of the influence of sociological variables of children born SGA in the last decade in Basque Country | Ignacio Diez | Received |
|
|||
| 890-P3-D2 | A novel mutation causing Pseudohypoaldosteronsim | Emmeline Heffernan | Received |
|
|||
| 891-P3-D2 | A novel mutation in the NR3C2 gene causing Pseudohypoaldosteronism Type 1 | Amalia Sertedaki | Received |
|
|||
| 892-P3-D2 | Subcutaneous fat necrosis causing prolonged hypercalcaemia in a neonate: An unusual case | Usha Niranjan | Received |
|
|||
| 894-P3-D2 | Relationship of birth gestational age with Insulin-like Growth Factor Binding Protein-3 beyond influences of gender, small-for-gestational-age status, caesarean section, caloric intake, parenteral nutirtion and predominant breast milk | cesare terzi | Received |
|
|||
| 895-P3-D2 | Relationship of birth gestational age with the ratio between Insulin-like Growth Factor-II and Insulin-like Growth factor Binding Protein-3 in blood serum beyond influences of gender, small-for-gestational-age status, caesarean section, | cesare terzi | Received |
|
|||
| 897-P3-D2 | TRANSIENT NEONATAL DIABETES MELLITUS: New Case | SUNA HANC&304;L&304; | Received |
|
|||
| 898-P3-D2 | NEONATAL MARFAN SYNDROME: A CASE REPORT | María Magdalena Hawkins | Received |
|
|||
| 899-P3-D2 | Iodine status in the neonate and the effect on thyroid function | Jeesuk Yu | Received |
|
|||
| 900-P3-D1 | Effect of Pubertal status, Age and Gender on Cortisol Response to Insulin Induced Hypoglycaemia in Children and Adolescents. | Dinesh Giri | Received |
|
|||
| 902-P3-D1 | A Case of Congenital Isolated Adrenocorticotropin Deficiency due to TPIT(TBX19) Gene Mutation | Nataliia Kazachenko | Received |
|
|||
| 905-P3-D1 | Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimotos thyroiditis | Wasniewska Malgorzata | Received |
|
|||
| 906-P3-D1 | Pituitary dysfunctiona with associated lesions in the hypothalamo-pituitary region: Histiocytosis or dysgerminoma? | ELPIS VLACHOPAPADOPOULOU | Received |
|
|||
| 908-P3-D1 | MACROPROLACTINOMA IN ADOLESCENCE: A CASE REPORT | Amanda Scott | Received |
|
|||
| 909-P3-D1 | Idiopathic central diabetes insipidus: a case of pediatric xhantogranuloma | gabriella pozzobon | Received |
|
|||
| 910-P3-D1 | Central Diabetes Insipidus caused by congenital cytomegalovirus: a rare association | TIAGO JERONIMO DOS SANTOS | Received |
|
|||
| 911-P3-D1 | Primary Polydipsia in a family with mutation in the AVP gene and proven central Diabetes Insipidus | Ruth Casey | Received |
|
|||
| 912-P3-D3 | Screening for SOX2 mutations in Bulgarian patients with congenital hyposomatotropism: first results | Ani Aroyo | Received |
|
|||
| 913-P3-D3 | Follow up for adult height of girl with the onset of puberty at 6 or 7 years old | Zhuang-Jian Xu | Received |
|
|||
| 914-P3-D3 | The influence of specimen pH on urinary LH and FSH by immunochemiluminometric assays | Ya-Ping Ma | Received |
|
|||
| 917-P3-D3 | MULTIPLE PITUITARY HORMONE DEFICIENCY (MPHD) WITH TRANSITORY PITUITARY ENLARGEMENT DUE TO PROP-1 MUTATION (CASE PRESENTATION) | Lavinia La Grasta Saboli&263; | Received |
|
|||
| 918-P3-D3 | MRI in children with growth hormone deficiency: | BAZ OUIDAD | Received |
|
|||
| 920-P3-D3 | A case of hypopituitarism caused by traumatic brain injury in infancy | Shinji Higuchi | Received |
|
|||
| 921-P3-D3 | Severe Features of Central Hypothyroidism und Hypoadrenalism effectively resolved by Treatment with Somatropin in a Boy with Panhypopituitarism | Gunter imi&263;-Schleicher | Received |
|
|||
| 922-P3-D3 | A case of combined pituitary hormone deficiency (CPHD) due to anterior pituitary hypoplasia | Ekaterine Kvaratskhelia | Received |
|
|||
| 923-P3-D3 | Think Histiocytosis X facing insipid diabetes with thickened pituitary stalk | Lydia Lichtenberger | Received |
|
|||
| 925-P3-D1 | The timing and evolution of puberty in a sample of school-aged children in a Brazilian city | Taciana Carla Maia Feibelmann | Received |
|
|||
| 928-P3-D1 | CHARACTERISTICS OF CHILDREN TREATED WITH LEUPROLIDE ACETATE | Gulcan Seymen Karabulut | Received |
|
|||
| 929-P3-D1 | Long term consequences of indirect topical exposure to testosterone gel in young children. | Inge Gies | Received |
|
|||
| 930-P3-D1 | FINAL HEIGHT IN GIRLS WITH IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY TREATED WITH GNRH ANALOG: COMPARISON WITH UNTREATED CONTROLS | Zeynep Atay | Received |
|
|||
| 931-P3-D1 | X-linked recessive form of Nephrogenic Diabetes Insipidus in a 7 year old boy | Aleksandra Janchevska | Received |
|
|||
| 932-P3-D1 | Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation | eda mengen uaktrk | Received |
|
|||
| 936-P3-D1 | ASSOCIATION OF VAN WYK GRUMBACH AND DEBRE SEMELAIGNE SYNDROMES IN TWO CASES WITH SEVERE HYPOTHROIDISM | Fatma Demirel | Received |
|
|||
| 938-P3-D3 | Hyperandrogenism doesnt increase the insulin resistance in overweight and obese adolescent girls with polycystic ovary syndrome | Natalija Smetanina | Received |
|
|||
| 939-P3-D3 | Precocious Puberty due to Duplication of the Pituitary Gland | Carla Minutti | Received |
|
|||
| 940-P3-D3 | Inhibin B in the boys with constitutional delay of puberty: relationship with gonadotropins, testosterone and anti-mllerian factor | Latyshev Oleg | Received |
|
|||
| 941-P3-D3 | A rare cause of peripheric precocious puberty: Adrenocortical tumor | Erkan Sari | Received |
|
|||
| 942-P3-D3 | A severe LHRH-independent precocious puberty in a 26-month-old girl with aclinical diagnosis of McCune-Albright Syndrome. | Maciej Flader | Received |
|
|||
| 944-P3-D3 | Central precocious puberty and autism: 3 cases report | Daniela Amaral | Received |
|
|||
| 947-P3-D3 | The Etiology of Central Precocious Puberty (CPP) and Effect of Gonadotropin Releasing Hormone (GnRH) Agonist for 2 years in Korean Boys | Young Suk Shim | Received |
|
|||
| 948-P3-D3 | Hypothalamic hamartoma as a cause of central precocious puberty in 4,5-year old girl-case report | Ewa Jakubowska | Received |
|
|||
| 949-P3-D3 | The perception of body image and self-esteem in girls with precocious puberty, being treatment with GnRH analogue | Eun Young Kim | Received |
|
|||
| 950-P3-D3 | LEYDIG CELL HYPERPLASIA MIMICKING TUMOR: A RARE CAUSE OF ISOSEXUAL PRECOCCIOUS PUBERTY | Glcan Seymen Karabulut | Received |
|
|||
| 952-P3-D1 | Discordant genotypic sex and concordant phenotypes in two Spanish siblings with 17a-hydroxylase/17,20-lyase deficiency carrying the most prevalent mutated alleles in Brazilian patients | Audi Laura | Received |
|
|||
| 953-P3-D1 | The development of gonadoblastoma in a 3-year-old girl with 46X,del(Y)p11.3, gonadal dysgenesis and associated congenital anomalies. | Zofia Kolesi&324;ska | Received |
|
|||
| 954-P3-D1 | 46,XX DSD: bilateral ovotestis with SOX9 | Gianni Russo | Received |
|
|||
| 955-P3-D1 | Severe undervirilisation in a 46,XY case due to a novel mutation in HSD17B3 gene | Ayfer Alikasifoglu | Received |
|
|||
| 957-P3-D1 | 5a-Steroid Reductase 2 Deficiency in a Large Family | eda mengen uaktrk | Received |
|
|||
| 958-P3-D1 | 17HSD-3 Enzyme Deficiency in Newborn due to A Novel Mutation in HSD17B3 Gene | ELIF SAGSAK | Received |
|
|||
| 959-P3-D1 | Partial androgen insensitivity syndrome in a boy with inactivating androgen receptor mutation and somatic mosaicism | Johanna Tommiska | Received |
|
|||
| 960-P3-D1 | CLINICAL CHARACTERISTICS OF 30 PATIENTS WITH 45,X/46,XY MOSAICISM | SUKRAN POYRAZOGLU | Received |
|
|||
| 961-P3-D1 | Three Siblings extremely Androgen Insensitivity Syndrome due to an AR mutation with Differing Phenotypes | bilgin yuksel | Received |
|
|||
| 962-P3-D1 | 46,XY Female with Turner Syndrome, Crohns Disease and low level mosaicism formonosomy X | Emir Tas | Received |
|
|||
| 963-P3-D2 | HYPOSPADIAS IN A MALE PATIENT WITH 21-HYDROXYLASE DEFICIENCY AND ATYPICAL CLINICAL COURSE: PRESENTATION OF TWO BROTHERS | suna hancili | Received |
|
|||
| 964-P3-D2 | An ovulating testis | Jaya Sujatha Gopal Kothandapani | Received |
|
|||
| 965-P3-D2 | Mosaicism ratios of 45,X to 46,X idicY can explaine a phenotype in a case with mixed gonadal dysgenesis. | Megumi Hatano | Received |
|
|||
| 966-P3-D2 | A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation | Bumin Nuri Dundar | Received |
|
|||
| 967-P3-D2 | Phenotypic and genotypic variability of patients with 5-a reductase type 2 deficiency | Kun Hu | Received |
|
|||
| 968-P3-D2 | The Novel Mutation in the Steroidogenic Acute Regulatory Protein (StAR) in 46, XY Case with Adrenal Insufficiency and Complete Sex Reversal | Fatih Gurbuz | Received |
|
|||
| 969-P3-D2 | A challenging diagnosis in three 46, XY females from two related families. | Raffaella Di Mase | Received |
|
|||
| 970-P3-D2 | A familial case of complete androgen insensitivity syndrome | Evelina Maines | Received |
|
|||
| 971-P3-D2 | A case of 46,Y,dup(X)(p21.2p22.2) DSD caused by overexpressed DAX1 | sasaki Takako | Received |
|
|||
| 977-P3-D1 | Neonatal Thyrotoxicosis in Maternal Graves Disease: A Case Series and Review of the Literature | Niall Johnston | Received |
|
|||
| 980-P3-D1 | Diagnostic challenges of Thyroid dysfunction in Eating Disorders | Priyha Santhanam | Received |
|
|||
| 981-P3-D1 | KocherDebréSemelaigne syndrome with rhabdomyolysis and increased creatinine: a case report. | Emine Ayca Cimbek | Received |
|
|||
| 982-P3-D1 | Preliminary results and normative TSH values for healthy Nigerian newborn children | IRORO YARHERE | Received |
|
|||
| 983-P3-D1 | Resistance to Thyroid Hormone Syndrome from childhood to adulthood variation in symptoms and thyroid function | Aoife Garrahy | Received |
|
|||
| 985-P3-D1 | Trends in incidence of permanent and transient congenital hypothyroidism in Shanghai China | XIN FAN | Received |
|
|||
| 986-P3-D1 | Klippel-Feil syndrome and thyroiditis: a case report | Elisa Guidoni | Received |
|
|||
| 987-P3-D2 | The association of thyroid dysfunction and blood pressure in Korean children | Hae Soon Kim | Received |
|
|||
| 989-P3-D2 | Aetiology and different clinical conditionsof hyperthyroidism in children and adolescents | Fadila Bouferoua | Received |
|
|||
| 991-P3-D2 | MISSED CASES OF CONGENITAL HYPOTHYROIDISM DETECTED BY SCREENING PROGRAM IN CENTRAL SERBIA (1983-2014) | Sladjana Todorovic | Received |
|
|||
| 993-P3-D2 | Raised free thyroxine levels in a boy with hypertension. | Sharon Lim | Received |
|
|||
| 994-P3-D2 | THE EVALUATION OF TRANSIENT HYPOTHYROIDISM IN PATIENTS DIAGNOSED WITH CONGENITAL HYPOTHYROIDISM | Havva Nur Peltek Kendirci | Received |
|
|||
| 995-P3-D2 | Optimizing treatment in congenital hypothyroidism | Joana Caetano | Received |
|
|||
| 997-P3-D2 | Delayed Diagnosis of Congenital Hypothyroidism (CH) and consequences: A case series | Tamunopriye Jaja | Received |
|
|||
| 1000-P3-D2 | Changes of laboratory findings before and after thyroid hormone replacement in a nave 19.24 year-old female case of ectopic thyroid | Joong Wan Choi | Received |
|
|||
53rd Annual ESPE Meeting 2014
18-20 September 2014 DUBLIN
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ACTIVE FROM 13/09/2014 TO 23/09/2016
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DOI: 10.3252/pso.eu.53espe.2014 
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