EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

53rd Annual ESPE Meeting 2014

 

18-20 September 2014 DUBLIN
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Poster title
Applicant name
Status
  621-P3-D1 The effect of working in a childrens hospital on urinary catecholamine excretion rates in male and female physicians Claudia Boettcher Received Received
  622-P3-D1 Body Composition Analysis in Girls with Premature Adrenarche Ayse Nurcan Cebeci Received Received
  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 Received
  627-P3-D1 A Rare Cause of Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency: A Case Report peyami cinaz Received Received
  629-P3-D1 Clinical and genetic diagnosis of Allgrove syndrome Zdravka Todorova Received Received
  630-P3-D1 Clinical case of Cushing syndrome in secreting NET GIANLUCA MUSOLINO Received Received
  632-P3-D1 Secondary Pseudohypoaldosteronism Type 1 the role of a Urinary Steroid Profile in diagnosis. Mariana Grace Received Received
  633-P3-D1 Steroid 11Hydroxylase deficiency in Egyptian children Noha Musa Received Received
  634-P3-D2 PRENATAL DEXAMETHASONE USE FOR THE PREVENTION OF VIRILIZATION IN PREGNANCY AT RISK FOR CLASSICAL CONGENITAL ADRENAL HYPERPLASIA María Sanz Fernández Received Received
  635-P3-D2 Congenital Adrenal Hyperplasia- Survey of the management in children across U.K Usha Niranjan Received Received
  636-P3-D2 Neonatal hpercalcaemia associated with congenital adrenal hyperplasia Cigdem Binay Received Received
  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 Received
  640-P3-D2 Therapeutic troubles of Cushings disease in adolescence: report of a case MANUELA DEIANA Received Received
  641-P3-D2 Congenital Hypoaldosteronism of Unknown Etiology in Five Half-Siblings Jan Foote Received Received
  642-P3-D2 X-linked adrenoleukodystrophy in 8 patients. Zhe Meng Received Received
  644-P3-D2 Cushing Syndrome without origin Sara Queirolo Received Received
  645-P3-D2 Untreated congenital adrenal hyperplasia with central precocious puberty Mihaela Dimitrova Received Received
  646-P3-D3 Hypothyroidism in anorexia nervosa due to primary autoimmune pathogenesis Rajesh Chidanandaswamy Received Received
  647-P3-D3 Autoimmune disease and Arnold Chiari Syndrome: any correlation? Elvira Piccinno Received Received
  648-P3-D3 Genetically proven APS type 1 in two siblings Desislava Yordanova Received Received
  649-P3-D3 Rare association of diabetes insipidus and autoimmune thyroiditis in 11-year-old girl Mirjana Kocova Received Received
  651-P3-D3 Diabetes mellitus after hematopoietic stem cell transplantation karla maria narvaez barros Received Received
  652-P3-D3 PRESERVATION OF OVARIAN FUNCTION IN YOUNG FEMALES CANCER SURVIVORS WITH RISK OF OVARIAN FAILURE Maria J. Chueca Guindulain Received Received
  653-P3-D3 Late endocrine effects in children and adolescentes submitted to allogenic bona marrow tranplantation HILTON KUPERMAN Received Received
  654-P3-D3 Adrenocortical tumor: a case report Elisa Guidoni Received Received
  655-P3-D3 A conservative approach to the management of endocrine neoplasia in Carney Complex in an adolescent male Carley Frerichs Received Received
  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 Received
  663-P3-D1 HYPOVITAMINOSIS D: FACTORS AFFECTING IN SPANISH CHILDREN AND ADOLESCENTS Maria Rosaura Leis Received Received
  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 Received
  666-P3-D1 Hypercalciuria in Patients with Coexisting Osteogenesis Imperfecta and Renal Tubular Acidosis Luisa Aguiar Received Received
  667-P3-D1 METABOLIC AND BONE DISORDERS IN VERTICALLY HIV-INFECTED CHILDREN maritza vivanco Received Received
  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 Received
  671-P3-D1 A Challenging Diagnosis of Pseudohypoparathyroidism type 1a and practical management: a case report Mariana Grace Received Received
  675-P3-D2 FGFR3 GENE: A VERY RARE MUTATION María Magdalena Hawkins Received Received
  677-P3-D2 Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets Melik&351;ah Keskin Received Received
  678-P3-D2 When is epilepsy not epilepsy Richard Lloyd-Nash Received Received
  679-P3-D2 Evaluation of Patients with Stunting in Armenia Renata Markosyan Received Received
  680-P3-D2 Fluctuation in cerebral calcification in a patient with pseudohypoparathyroidism type II Elena Sukarova-Angelovska Received Received
  681-P3-D2 VARIABILITY IN CLINICAL AND GENETIC SPECTRUM IN HYPOPHOSPHATASIA: NATURAL HISTORY IN TWO PATIENTS Gabriel Á. Martos-Moreno Received Received
  682-P3-D2 Cautionary Tales in the Management of Transient Neonatal Hypoparathyroidism Ian Mulvey Received Received
  684-P3-D2 Clinical phenotype and molecular studies in patients with hypophosphatemic rickets Monika Obara-Moszynska Received Received
  685-P3-D2 Autosomal-dominant hypocalcaemia, new clinical features Noemi Fuentes-Bolaños Received Received
  686-P3-D3 Bone Health in a cohort of Irish Spinal Muscular Atrophy (SMA) Patients Niamh Mc Sweeney Received Received
  686-P3-D2 Intravenous Zoledronic Acid: Experience of Treatment of Children with Osteogenesis Imperfecta in Indonesia Dwi Lestari Pramesti Received Received
  687-P3-D3 Endocrinological assessment of children with bronchiectasis Ilker Tolga Ozgen Received Received
  688-P3-D3 Mutational analysis of TAC and TAC3 in idiopathic central precocious puberty Marina Krstevska-Konstantinova Received Received
  689-P3-D3 Vitamin D levels in short prepubertal children born small for gestational age (SGA) Maria Korpal-Szczyrska Received Received
  690-P3-D3 Prospective evaluation of bone mineralization, PTH regulation and metabolic profile in adult patients with hereditary hypophosphatemic rickets. emese boros Received Received
  691-P3-D3 Bone mineral density and vitamine D status in girls and adolescents with Turner Syndrome: BAZ OUIDAD Received Received
  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 Received
  694-P3-D3 McCune-Albright Syndrome associated to hypophosphatemic rickets TIAGO JERONIMO DOS SANTOS Received Received
  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 Received
  697-P3-D3 A CASE WITH ODONTOHYPOPHOSPHATASIA AND FAMILY INVESTIGATION Esra Deniz Papatya Cak&305;r Received Received
  698-P3-D3 TSH/fT4 ratio as a marker of TSH resistance in Pseudoparathyroidism 1A and obesity Aurélia Alimi Received Received
  699-P3-D3 Infantile hypophosphatasia Nevenka Slaveska Received Received
  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 Received
  701-P3-D1 Changing Presentation of Type 1 Diabetes to a Tertiary Paediatric Centre Niamh Mc Grath Received Received
  703-P3-D1 Urinary C-Peptid/Creatinine Ratio in Children and Adolescents Diagnosed withMaturity-Onset Diabetes of the Young (MODY) Sebahat Yilmaz Agladioglu Received Received
  704-P3-D1 A case with neonatal diabetes and congenital hypothyroidism due to GLIS3 gene deletion Ilker Tolga Ozgen Received Received
  705-P3-D1 Glycemic control of patients with type 1 Diabetes using automated bolus calculator glucometer Jaime Cruz Rojo Received Received
  708-P3-D1 Clinical significance of typing fulminant type 1 diabetes in children and adolescents wang yi Received Received
  709-P3-D1 Continuous Subcutaneous Insulin Infusion Therapy in Preschool Children with Type 1 Diabetes Mellitus Rita Moinho Received Received
  712-P3-D2 Audit of the use of integrated care pathway in the management of Diabetic keto acidosis in children Ravi Palakurthi Received Received
  713-P3-D2 Development of diabetes mellitus after hematopoietic stem cell transplantation for childhood leukemia In Ah Jung Received Received
  714-P3-D2 Case of family neonatal diabetes with KCNJ11 gene mutation Svitlana Chumak Received Received
  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 Received
  718-P3-D2 INCIDENCE OF DIABETES MELLITUS AND ASSOCIATED COMPLICATIONS AMONG CHILDREN: RESULTS FROM AZERBAIJAN DIABETES REGISTRY 1997-2007 Gunduz Ahmadov Received Received
  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 Received
  720-P3-D2 ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODIES ARE NOT FREQUENT IN CHILDREN WITH TYPE 1 DIABETES Melek Y&305;ld&305;z Received Received
  721-P3-D2 GLYCEMIC VARIABILITY AND METABOLIC CONTROL IN PEDIATRIC PATIENTS WITH TYPE 1 DIABETES MELLITUS María Martín-Frías Received Received
  722-P3-D2 Knowledge base and attitudes of senior medical staff to insulin therapy in children with diabetes Amith Nuti Received Received
  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 Received
  725-P3-D3 Differences in pubertal development and anthropometry between normal population and type1 diabetic child at debut in Spain Ignacio Diez Received Received
  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 Received
  727-P3-D3 Evaluation of HbA1c measurement in Trinidad and Tobago Maynika Rastogi Received Received
  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 Received
  730-P3-D3 Wolcott-Rallison Syndrome In Two Siblings With No Implication Of EIF2AK3 Mutation AYCA ALTINCIK Received Received
  731-P3-D3 Prevalence of atopic diseases in diabetic children and adolescents Hildegard Jasser-Nitsche Received Received
  732-P3-D3 The Pattern of Body Composition Change in Type 1 Diabetes by Gender Yong Hyuk Kim Received Received
  733-P3-D3 Transient Neonatal Diabetes and intermediate DEND phenotype with KCNJ11 mutation Ana Laura Fitas Received Received
  735-P3-D3 Metabolic control in a pediatric population with type 1 diabetes mellitus Joana Verdelho Andrade Received Received
  736-P3-D2 Metabolic compensation correlation with chronic complications of type 1 diabetes in children in Latvia Zane Eglite Received Received
  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 Received
  738-P3-D2 When should we suspect maturity onset diabetes of the young in children and adolescents? Sarar Mohamed Received Received
  740-P3-D2 Continuous Glucose Monitoring System (CGMS) in the Diagnosis of Early Glycemic Abnormalities in High Risk Groups Ashraf Soliman Received Received
  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 Received
  742-P3-D2 Learning by doing approach: use of multimedia applications in type 1 diabetic children. Elvira Piccinno Received Received
  743-P3-D2 Seip Berardinelli Syndrome Case Report DOLY PANTOJA Received Received
  744-P3-D2 9-year old boy with Wolfram syndrome - case report Ewa Jakubowska Received Received
  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 Received
  748-P3-D3 Monogenic Diabetes in a Paediatric Population: finding the needle in the haystack. Meenal Mavinkurve Received Received
  749-P3-D3 Hyperglycemia MODY a diagnosis to remember Ricardo Monteiro Received Received
  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 Received
  752-P3-D3 The psychological impact of diabetes on glycaemic control in affected Saudi children at different developmental age groups Amir Babiker Received Received
  753-P3-D3 Type 1 diabetes mellitus in pediatric population: chronic complications and associated diseases Joana Verdelho Andrade Received Received
  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 Received
  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 Received
  757-P3-D3 Pneumothorax, pneumomediastinum and subcutaneous emphysema: complications of severe DKA in T2DM obese patient. Elvira Piccinno Received Received
  759-P3-D3 Diabetes mellitus type 2 in Pediatrics : an emerging reality in our country. First cases described at Spain Ignacio Diez Received Received
  760-P3-D1 Association of Ghrelin Gene Polymorphisms with Obesity in Japanese Children Ikuyo Itoh Received Received
  763-P3-D1 Association of lifestyle with metabolic syndrome in children Andrea Paola Rojas Gil Received Received
  766-P3-D1 Positive association of pro-oxidative stress markers with adipose mass in pre- and early-pubertal boys George Paltoglou Received Received
  767-P3-D1 Prevalence metabolic syndrome and its components among children with obesity Latyshev Oleg Received Received
  771-P3-D1 Level of non-high-density-lipoprotein cholesterol and its related factors in Chinese Han students Yanlan Fang Received Received
  773-P3-D2 Trends in obesity prevalence and body-mass index among pre-pubertal Bulgarian children, 1990-2007 violeta Iotova Received Received
  774-P3-D2 The prevalence of 25-hydroxyvitamin D insufficiency and deficiency among overweight and obese children and adolescents in Greece. Christos Giannios Received Received
  775-P3-D2 Metabolic and lifestyle correlates of health-related quality of life among Taiwanese obese adolescents Meng-Che Tsai Received Received
  776-P3-D2 Prevalence of Dyslipidemia and Associated Factors Among Obese Turkish Children Selin Elmaogullari Received Received
  779-P3-D2 Belma Haliloglu Received Received
  781-P3-D2 Relationship between adiposity degree and physical activity and inactivity among children and adolescents Maria Rosaura Leis Received Received
  782-P3-D2 Antenatal and early childhood determinants of the development of obesity in children Yauhenia Dzmitrovich Received Received
  783-P3-D2 The association hypothyroidism obesity in a group of children and adolescents Mirela Mogoi Received Received
  784-P3-D2 A new lipodystrophy syndrome? Julia von Schnurbein Received Received
  786-P3-D3 Hypothalamic Obesity in Children and Adolescents: a multi-disciplinary approach and novel therapeutic tools. DANIELE TESSARIS Received Received
  789-P3-D3 Bone age advancement in prepubertal children with overweight and obesity Hae Sang Lee Received Received
  790-P3-D3 Obesity correlates in adolescence Papandreou Ioannis Received Received
  793-P3-D3 Prevalence of abnormalities of glucose metabolism in obese Greek children and adolescents Karachaliou Feneli Received Received
  794-P3-D3 PRADER WILLI SYNDROME (PWS): REPORTS OF TWO PATIENTS WITH CONGENITAL ABNORMALITIES OF KIDNEY AND URINARY TRACT. federica tamburrino Received Received
  795-P3-D3 RESPONSE TO TREATMENT IN A GROUP OF PATIENTS WITH CHILDHOOD OBESITY. concepcion freijo martin Received Received
  796-P3-D3 PREVALENCE OF OVERWEIGHT AND OBESITY IN CHILDREN AND ADOLESCENTS AT PUBLIC AND PRIVATE SCHOOLS FROM UBERABA BRAZIL Adriana Paula Silva Received Received
  798-P3-D3 Characteristics of a Population of Obese Children and Adolescents: Suggesting a new paradigm. Quentin Van Meter Received Received
  799-P3-D3 EFFECTS OF GnRH ANALOGUE TREATMENT ON INTERNAL GENITALES OF GIRLS WITH CENTRAL PRECOCIOUS HAVVA NUR PELTEK KENDERCI Received Received
  801-P3-D3 The usefulness of the Leuprolide stimulation test as a diagnostic method of idiopathic CPP in girls. Marta Murillo Vallés Received Received
  803-P3-D3 Menstrual Regularity among Early Menarche girls and CPP or EFP girls treated with GnRHa CHEN Qiu-Li Received Received
  804-P3-D3 COMPLETE BLOOD COUNT PARAMETERS IN GIRLS WITH POLYCYSTIC OVARY SYNDROME AHMET UCAKTURK Received Received
  805-P3-D3 The Genotypic and Phenotypic Variability of Mixed Gonadal Dysgenesis Chelsey Grimbly Received Received
  806-P3-D3 A rare cause for 46,XX ovarian dysgenesis: Perrault syndrome Glay Karagzel Received Received
  807-P3-D3 A rare cause of ovarian failure; ovarioleucodystrophy Erkan Sari Received Received
  809-P3-D3 THREE SIBLINGS WITH GONADAL DYSGENESIS Fatma Dursun Received Received
  810-P3-D1 The role of IGF-IR gene mutation in the development of Oligodendrocytes Fan Yang Received Received
  811-P3-D1 A Novel GHR mutation,c.4391GA;in a Family with Laron syndrome Sameh Tawfik Received Received
  813-P3-D1 Body Mass Index, IGF1-SDS and rhGH treatment Ioannis- Anargyros Vasilakis Received Received
  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 Received
  818-P3-D1 Assessment of compliance with Growth Hormone (GH) therapy. Chrysoula Drosatou Received Received
  819-P3-D1 Body composition in GH deficient children: effects of GH therapy and comparison between DXA and anthropometric data. Mariacarolina Salerno Received Received
  821-P3-D1 Study of Growth Hormone Receptor(GHR)exon 3 polymorphism in children with Prader-Willi Syndrome WEI LU Received Received
  822-P3-D1 Auxological evaluation of non-identical twins Pop Raluca-Monica Received Received
  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 Received
  823-P3-D1 3-years height outcome during rh-growth hormone therapy in severe short subjects affected by skeletal dysplasias Francesco Massart Received Received
  824-P3-D2 Growth hormone deficiency in a case with Neurofibromatosis-Noonan Syndrome (NFNS) Dogus Vuralli Received Received
  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 Received
  826-P3-D2 Usability and safety of FlexPro PenMate in patients, caregivers and healthcare professionals Anne-Marie Kappelgaard Received Received
  827-P3-D2 Impairment of glucose metabolism in Growth Hormone (GH) deficient children under GH replacement MARIA CHATZIPSALTI Received Received
  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 Received
  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 Received
  830-P3-D2 Prader Willi Syndrome and growth hormone therapy: valuable effects and adverse events Magdalena Wilk Received Received
  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 Received
  833-P3-D2 GROWTH HORMONE TREATMENT IN 50 CHILD WITH SHORT STATURE: LEBANESE EXPERIENCE. ABI NADER ELIE Received Received
  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 Received
  835-P3-D2 An unusual case of a child with Growth Hormone Deficiency and Arnold-Chiari malformation type I. MARIA CHATZIPSALTI Received Received
  836-P3-D3 WHAT IS THE PROFIL OF GIGANTISM :7 observations achir samia Received Received
  837-P3-D3 GH treatment in Dents disease: a case report Elisa Guidoni Received Received
  838-P3-D3 ANALYSIS OF THE EFFECTIVENESS OF GROWTH HORMONE TREATMENT IN A TERTIARY HOSPITAL IN THE LAST 30 YEARS Jaime Cruz Rojo Received Received
  839-P3-D3 A Rare Syndrome Benefits From Growth Hormone Therapy: Hypotonia-Cystinuria Syndrome Onur Akin Received Received
  840-P3-D3 Changes in body mass index in GHD and SGA children in the first year of treatment Llano Juan Pablo Received Received
  841-P3-D3 Study of the effect of growth hormone treatment on growth in patients with methylmalonic acidemia. Dirk De Weerdt Received Received
  843-P3-D3 TWO YEARS OF GROWTH HORMONE THERAPY IN CHILDREN WITH GROWTH DEFICIENCY mimouna bessahraoui Received Received
  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 Received
  846-P3-D3 Design and Recruitment of a Longitudinal Cohort Study of Growth and Puberty in Russian Boys Oleg Sergeyev Received Received
  848-P3-D3 Severe short stature with features of achondroplasia, later diagnosed as panhypopituitarism - a case report Cristina Matei Received Received
  849-P3-D2 Growth Hormone Therapy in Prepubertal Children Results after 4 years Corina Galesanu Received 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 Received
  851-P3-D2 Growth pattern of the Nigerian child compared to International references Chizo Agwu Received 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 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 Received
  854-P3-D2 Descriptive Analysis of Medication Adherence for Patients Treated with Growth Hormone Therapy Julie Locklear Received Received
  855-P3-D2 EFFECT OF CONGENITAL HEART DISEASE ON PLACENTAL AND BIRTH SIZE. Ashraf Soliman Received 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 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 Received
  864-P3-D3 The Establishment of a New Paediatric Endocrinology Training Programme in South Africa Franois de Villiers Received Received
  866-P3-D3 Growth hormone treatment adherence in children in Latvia Zane Eglite Received Received
  867-P3-D3 The effect of GH and pubertal induction therapy in Turner Syndrome. &350;kran Darkan Received Received
  868-P3-D3 Hearing loss in Turner syndrome BAZ OUIDAD Received Received
  869-P3-D3 Genotype-Phenotype Correlation in Turner Syndrome adel djermane Received Received
  870-P3-D3 Primary amenorrhea with normal stature: why not Turner syndrome? IOANA HRISTOV Received Received
  871-P3-D3 The causes of short stature in Turner syndrome Ruimin Chen Received Received
  877-P3-D1 CONGENITAL HYPERINSULINISM: CLINICAL AND MOLECULAR CHARACTERISTICS OF BRAZILIAN PATIENTS Raphael Liberatore Junior Received Received
  879-P3-D1 Congenital Hyperinsulinism: A Single-Center Experience Murat Dogan Received Received
  880-P3-D1 Persistent hyperinsulinemic hypoglycemia of an infancy carrying ABCC8 Arg598stop mutation Jianfang Zhu Received Received
  881-P3-D1 A Case of Hyperinsulinism/hyperammonemia Syndrome. Young Suk Shim Received Received
  882-P3-D1 PROJECT epiSGA - PreMeb . Presentation , subject recruitment and initial data Ignacio Diez Received Received
  885-P3-D1 Neonatal seizures neonatal due to hypocalcemia secondary to maternal vitamin D deficiency ARIADNA CAMPOS MARTORELL Received Received
  888-P3-D2 Neonatal Neurogenic Diabetes Insipidus a case report INS ALVES Received 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 Received
  890-P3-D2 A novel mutation causing Pseudohypoaldosteronsim Emmeline Heffernan Received Received
  891-P3-D2 A novel mutation in the NR3C2 gene causing Pseudohypoaldosteronism Type 1 Amalia Sertedaki Received Received
  892-P3-D2 Subcutaneous fat necrosis causing prolonged hypercalcaemia in a neonate: An unusual case Usha Niranjan Received 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 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 Received
  897-P3-D2 TRANSIENT NEONATAL DIABETES MELLITUS: New Case SUNA HANC&304;L&304; Received Received
  898-P3-D2 NEONATAL MARFAN SYNDROME: A CASE REPORT María Magdalena Hawkins Received Received
  899-P3-D2 Iodine status in the neonate and the effect on thyroid function Jeesuk Yu Received 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 Received
  902-P3-D1 A Case of Congenital Isolated Adrenocorticotropin Deficiency due to TPIT(TBX19) Gene Mutation Nataliia Kazachenko Received Received
  905-P3-D1 Key-role of thyrotropin deficiency in disclosing craniopharyngioma diagnosis in a short girl with Hashimotos thyroiditis Wasniewska Malgorzata Received Received
  906-P3-D1 Pituitary dysfunctiona with associated lesions in the hypothalamo-pituitary region: Histiocytosis or dysgerminoma? ELPIS VLACHOPAPADOPOULOU Received Received
  908-P3-D1 MACROPROLACTINOMA IN ADOLESCENCE: A CASE REPORT Amanda Scott Received Received
  909-P3-D1 Idiopathic central diabetes insipidus: a case of pediatric xhantogranuloma gabriella pozzobon Received Received
  910-P3-D1 Central Diabetes Insipidus caused by congenital cytomegalovirus: a rare association TIAGO JERONIMO DOS SANTOS Received Received
  911-P3-D1 Primary Polydipsia in a family with mutation in the AVP gene and proven central Diabetes Insipidus Ruth Casey Received Received
  912-P3-D3 Screening for SOX2 mutations in Bulgarian patients with congenital hyposomatotropism: first results Ani Aroyo Received 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 Received
  914-P3-D3 The influence of specimen pH on urinary LH and FSH by immunochemiluminometric assays Ya-Ping Ma Received 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 Received
  918-P3-D3 MRI in children with growth hormone deficiency: BAZ OUIDAD Received Received
  920-P3-D3 A case of hypopituitarism caused by traumatic brain injury in infancy Shinji Higuchi Received 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 Received
  922-P3-D3 A case of combined pituitary hormone deficiency (CPHD) due to anterior pituitary hypoplasia Ekaterine Kvaratskhelia Received Received
  923-P3-D3 Think Histiocytosis X facing insipid diabetes with thickened pituitary stalk Lydia Lichtenberger Received 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 Received
  928-P3-D1 CHARACTERISTICS OF CHILDREN TREATED WITH LEUPROLIDE ACETATE Gulcan Seymen Karabulut Received Received
  929-P3-D1 Long term consequences of indirect topical exposure to testosterone gel in young children. Inge Gies Received Received
  930-P3-D1 FINAL HEIGHT IN GIRLS WITH IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY TREATED WITH GNRH ANALOG: COMPARISON WITH UNTREATED CONTROLS Zeynep Atay Received Received
  931-P3-D1 X-linked recessive form of Nephrogenic Diabetes Insipidus in a 7 year old boy Aleksandra Janchevska Received Received
  932-P3-D1 Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation eda mengen uaktrk Received Received
  936-P3-D1 ASSOCIATION OF VAN WYK GRUMBACH AND DEBRE SEMELAIGNE SYNDROMES IN TWO CASES WITH SEVERE HYPOTHROIDISM Fatma Demirel Received Received
  938-P3-D3 Hyperandrogenism doesnt increase the insulin resistance in overweight and obese adolescent girls with polycystic ovary syndrome Natalija Smetanina Received Received
  939-P3-D3 Precocious Puberty due to Duplication of the Pituitary Gland Carla Minutti Received 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 Received
  941-P3-D3 A rare cause of peripheric precocious puberty: Adrenocortical tumor Erkan Sari Received 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 Received
  944-P3-D3 Central precocious puberty and autism: 3 cases report Daniela Amaral Received 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 Received
  948-P3-D3 Hypothalamic hamartoma as a cause of central precocious puberty in 4,5-year old girl-case report Ewa Jakubowska Received 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 Received
  950-P3-D3 LEYDIG CELL HYPERPLASIA MIMICKING TUMOR: A RARE CAUSE OF ISOSEXUAL PRECOCCIOUS PUBERTY Glcan Seymen Karabulut Received 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 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 Received
  954-P3-D1 46,XX DSD: bilateral ovotestis with SOX9 Gianni Russo Received Received
  955-P3-D1 Severe undervirilisation in a 46,XY case due to a novel mutation in HSD17B3 gene Ayfer Alikasifoglu Received Received
  957-P3-D1 5a-Steroid Reductase 2 Deficiency in a Large Family eda mengen uaktrk Received Received
  958-P3-D1 17HSD-3 Enzyme Deficiency in Newborn due to A Novel Mutation in HSD17B3 Gene ELIF SAGSAK Received Received
  959-P3-D1 Partial androgen insensitivity syndrome in a boy with inactivating androgen receptor mutation and somatic mosaicism Johanna Tommiska Received Received
  960-P3-D1 CLINICAL CHARACTERISTICS OF 30 PATIENTS WITH 45,X/46,XY MOSAICISM SUKRAN POYRAZOGLU Received Received
  961-P3-D1 Three Siblings extremely Androgen Insensitivity Syndrome due to an AR mutation with Differing Phenotypes bilgin yuksel Received Received
  962-P3-D1 46,XY Female with Turner Syndrome, Crohns Disease and low level mosaicism formonosomy X Emir Tas Received Received
  963-P3-D2 HYPOSPADIAS IN A MALE PATIENT WITH 21-HYDROXYLASE DEFICIENCY AND ATYPICAL CLINICAL COURSE: PRESENTATION OF TWO BROTHERS suna hancili Received Received
  964-P3-D2 An ovulating testis Jaya Sujatha Gopal Kothandapani Received 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 Received
  966-P3-D2 A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation Bumin Nuri Dundar Received Received
  967-P3-D2 Phenotypic and genotypic variability of patients with 5-a reductase type 2 deficiency Kun Hu Received 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 Received
  969-P3-D2 A challenging diagnosis in three 46, XY females from two related families. Raffaella Di Mase Received Received
  970-P3-D2 A familial case of complete androgen insensitivity syndrome Evelina Maines Received Received
  971-P3-D2 A case of 46,Y,dup(X)(p21.2p22.2) DSD caused by overexpressed DAX1 sasaki Takako Received Received
  977-P3-D1 Neonatal Thyrotoxicosis in Maternal Graves Disease: A Case Series and Review of the Literature Niall Johnston Received Received
  980-P3-D1 Diagnostic challenges of Thyroid dysfunction in Eating Disorders Priyha Santhanam Received Received
  981-P3-D1 KocherDebréSemelaigne syndrome with rhabdomyolysis and increased creatinine: a case report. Emine Ayca Cimbek Received Received
  982-P3-D1 Preliminary results and normative TSH values for healthy Nigerian newborn children IRORO YARHERE Received Received
  983-P3-D1 Resistance to Thyroid Hormone Syndrome from childhood to adulthood variation in symptoms and thyroid function Aoife Garrahy Received Received
  985-P3-D1 Trends in incidence of permanent and transient congenital hypothyroidism in Shanghai China XIN FAN Received Received
  986-P3-D1 Klippel-Feil syndrome and thyroiditis: a case report Elisa Guidoni Received Received
  987-P3-D2 The association of thyroid dysfunction and blood pressure in Korean children Hae Soon Kim Received Received
  989-P3-D2 Aetiology and different clinical conditionsof hyperthyroidism in children and adolescents Fadila Bouferoua Received Received
  991-P3-D2 MISSED CASES OF CONGENITAL HYPOTHYROIDISM DETECTED BY SCREENING PROGRAM IN CENTRAL SERBIA (1983-2014) Sladjana Todorovic Received Received
  993-P3-D2 Raised free thyroxine levels in a boy with hypertension. Sharon Lim Received Received
  994-P3-D2 THE EVALUATION OF TRANSIENT HYPOTHYROIDISM IN PATIENTS DIAGNOSED WITH CONGENITAL HYPOTHYROIDISM Havva Nur Peltek Kendirci Received Received
  995-P3-D2 Optimizing treatment in congenital hypothyroidism Joana Caetano Received Received
  997-P3-D2 Delayed Diagnosis of Congenital Hypothyroidism (CH) and consequences: A case series Tamunopriye Jaja Received 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 Received
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EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

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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