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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

Growth

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
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Chronic Effects of Bisphenol A Administration on Growth Hormone Activity
College of Medicine & Health Sciences, Sultan Qbaoos University, ALKhoudh, Muscat, Oman
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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
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Abstract unavailable
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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
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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
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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
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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
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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
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