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54th Annual ESPE

Barcelona, Spain
01 Oct 2015 - 03 Oct 2015

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Barcelona, Spain; 1-3 October 2015 Further information

Poster Presentations Poster Category 1


Silver-Russell Syndrome without Body Asymmetry in Three Patients with Duplications of Maternally Derived Chromosome 11p15 Involving CDKN1C
aHamamatsu University School of Medicine, Hamamatsu, Japan; bShinshu University School of Medicine, Matsumoto, Japan; cNiigata University School of Medicine, Niigata, Japan; dSaitama Medical University, Saitama, Japan; eNational Research Institute for Child Health and Development, Tokyo, Japan
Chronic Effects of Bisphenol A Administration on Growth Hormone Activity
College of Medicine & Health Sciences, Sultan Qbaoos University, ALKhoudh, Muscat, Oman
Severe IGF1 Deficiency and Multi-Organ Autoimmune Disease Associated with Novel Germline STAT3 Mutations
aCentro de Investigaciones Endocrinológicas ‘Dr César Bergadá’ (CEDIE) CONICET – FEI – División de Endocrinología, Hospital de Niños Ricardo Gutiérrez, Buenos Aires, Argentina; bEndocrinología, Hospital Universitario Austral, Buenos Aires, Argentina; cInmunología, Hospital de Niños Ricardo Gutiérrez, Buenos Aires, Argentina; dDivision of BM transplantation and Immunodeficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; eDivision of Endocrinology, Cincinnati Center for Growth Disorders, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; fInstituto de Agrobiotecnología de Rosario (INDEAR), CONICET, Rosario, Argentina
Abstract unavailable
Various Imprinting Disorders Underlying Silver-Russell Syndrome-Compatible Phenotype
aDepartment of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan; bDepartment of Pediatrics, Aichi Human Service Center, Central Hospital, Aichi, Japan; cDepartment of Pediatrics, Nagoya City West Medical Center, Aich, Japan; dDepartment of Pediatrics, Yaizu City Hospital, Shizuoka, Japan; eDepartment of Neurology, Fukuoka University Faculty of Medicine, Fukuoka, Japan; fDepartment of Pediatrics, Hamamatsu University School of Medicine, Shizuoka, Japan
Ligase IV Deficiency Syndrome as a Cause of Microcephalic Primordial Dwarfism in Dizygotic Twins
aGeneva University Hospital, Pediatrics, Geneva, Switzerland; bGeneva University Hospital, Genetic Medicine and Laboratories, Geneva, Switzerland
High Frequency of Hypomorphic Allelic Haplotypes of the gh1 Proximal Promoter in Patients with Proportional Undergrowth and Isolated GH Deficiency
aHospital University La Paz, INGEMM, IdiPAZ, UAM, Madrid, Spain; bCIBER de Enfermedades Raras (CIBERER U753), ISCIII, Madrid, Spain; cDepartment of Paediatric Endocrinology, Hospital Universitario 12 de Octubre, Madrid, Spain; dDepartment of Paediatric Endocrinology, Hospital University Marqués de Valdecilla, Santander, Spain; eDepartment of Paediatrics, Hospital San Agustín, Avilés, Spain; fFundación de Alcorcón, Department of Paediatrics, Hospital University, Madrid, Spain; gDepartment of Paediatrics, Hospital Sta María del Rosell, Murcia, Spain; hDepartment of Paediatrics, Hospital La Mancha Centro, Ciudad Real, Spain; iDepartment of Paediatrics, Hospital Nuestra Sra. De Sonsoles, Ávila, Spain; jDepartment of Paediatrics, Hospital Clínico Universitario, Valladolid, Spain; kDepartment of Paediatrics, Hospital Infanta Cristina, Madrid, Spain; lDepartment of Paediatric Endocrinology, Hospital Gral. de Granollers, Barcelona, Spain; mDepartment of Endocrinology, Hospital Virgen de la Luz, Cuenca, Spain; nDepartment of Paediatric Endocrinology, Hospital University Ramón y Cajal, Madrid, Spain; oDepartment of Paediatric Endocrinology, Hospital University La Paz, Madrid, Spain
GH Excess in McCune-Albright Syndrome
aPediatric Endocrinology, Regina Margherita Children Hospital, University of Torino, Turin, Italy; bSkeletal Clinical Studies Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, USA
GH Hypersecretion in Children with NF1 and Optic Pathway Gliomas
aUnit of Endocrinology and Diabetes, Bambino Gesu Children’s Hospital, IRCCS, Rome, Italy; bRare Diseases and Medical Genetics, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy; cNeuroradiology Unit, Department of Imaging, Bambino Gesù Children’s Hospital, IRCSS, Rome, Italy; dDepartment of Pediatric Hematology-Oncology, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy