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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

Thyroid

Congenital Hypothyroidism in Twin Couples and Triplets
aItalian National Institute of Health, Rome, Italy; bVita-Salute University, IRCCS San Raffaele Hospital, Milan, Italy; cUniversity of Bologna, Bologna, Italy; dUniversity ‘La Sapienza’, Rome, Italy; eGaribaldi Hospital, Catania, Italy; fIRCCS Istituto Auxologico Italiano and University of Milan, Milan, Italy
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Th17 Cells in Children with Graves' Disease During Methimazole Treatment
aDepartment of Pediatric Endocrinology and Diabetology, Medical University, Lublin, Poland; bDepartment of Clinical Immunology and Immunotherapy, Medical University, Lublin, Poland
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Thyrocytes are Particularly well Protected Against Oxidative Stress Induced by H2O2
aInstitut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, IRIBHM, Bruxelles, Belgium; bFaculty of Medicine, Department of Endocrinology of Erasme Hospital, Université libre de Bruxelle, Bruxelles, Belgium
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Thyrocyte is Particularly Well Protected Against Oxidative Stress Induced by H2O2
aInstitut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire, IRIBHM, Bruxelles, Belgium; bDepartment of Endocrinology of Erasme Hospital, Faculty of Medicine, Université libre de Bruxelles, Bruxelles, Belgium
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Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born After In Vitro Fertilisation
aDepartment of Biochemical Laboratories, Institute of Child Health, Athens, Greece; bFirst Department of Pediatrics, Division of Endocrinology, Metabolism and Diabetes, Medical School, National and Kapodistrian University of Athens, Athens, Greece
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Transient vs Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-Term Data Can Help Formulate a Practical Prognostic Algorithm
aDepartment of Biochemical Laboratories, Institute of Child Health, Athens, Greece; bFirst Department of Pediatrics, Division of Endocrinology, Metabolism and Diabetes, Medical School, National and Kapodistrian University of Athens, Athens, Greece; cDepartment of Medical Laboratories, Technological and Educational Institute of Athens, Athens, Greece
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Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor [alpha] Mutations
aDivision of Pediatric Endocrinology, Dr Behçet Uz Children’s Hospital, Izmir, Turkey; bDivision of Pediatric Endocrinology, Dokuz Eylül University, Izmir, Turkey; cDepartment of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands; dDivision of Pediatric Endocrinology, Tepecik Education and Research Hospital, Izmir, Turkey; eDepartment of Psychiatry, Hacettepe University, Ankara, Turkey; fDivision of Pediatric Endocrinology, Eskisehir State Hospital, Eskisehir, Turkey; gDivision of Pediatric Endocrinology, Katip Çelebi University, Izmir, Turkey
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Intelligence and Behaviour in Children and Adolescents with Hashimoto's Thyroiditis
aPaediatric Endocrinology & Diabetology, Centre of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany; bPsychoanalytic Family Therapy, Centre of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany; cDepartment of Child Neurology, Centre of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany
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Brain-Lung-Thyroid Syndrome - Update on the Clinical Spectrum of a Heterogeneous Disorder
aDivision of Paediatric Endocrinology, University Children’s Hospital, Basel, Switzerland; bDepartment of Medical Genetics, University Hospital, Basel, Switzerland
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Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis
aPrivate Pediatrics and Pediatric Endocrinology Practice, Cracow, Poland; bDepartment of Pediatric and Adolescent Endocrinology, Chair of Pediatrics, Polish-American Institute of Pediatrics, Jagiellonian University Medical College (by 2014), Cracow, Poland; cDepartment of Pediatrics, Johannes Gutenberg University Medical School, Mainz, Germany; dDivision of Medical Genetics, Chair of Pediatrics, Polish-American Institute of Pediatrics, Medical College, Jagiellonian University, Cracow, Poland
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Severe Hyperthyroidism in an Infant Revealed a Familial Non-Autoimmune Hyperthyroidism with Novel Heterozygous Thyrotropin Receptor Gene Mutation
aUnité d’endocrinologie génétique maladies osseuses et gynécologie, hôpital des enfants, Toulouse, France; bLaboratoire de Biochimie et Biologie moléculaire, Institut Fédératif de Biologie, Toulouse Purpan, France; cService d’Endocrinologie et Maladies métaboliques, Hôpital Larrey, Toulouse, France
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