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57th Annual ESPE

Athens, Greece
27 Sep 2018 - 29 Sep 2018

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ESPE 2018 57th European Society for Paediatric Endocrinology Annual Meeting 27-29 September 2018 Athens, Greece

Poster Presentations

Thyroid P2

Long Term Monitoring of Graves Disease in Children and Adolescents: Single Center Experience
aDr. Behçet Uz Children’s Hospital, Clinic of Pediatric Endocrinology, İzmir, Turkey; bDicle University Faculty of Medicine Department of Bioistatistics, Diyarbakır, Turkey; cDokuz Eylül University Faculty of Medicine, Department of Pediatric Endocrinology, İzmir, Turkey
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The Prevalence of Clinically Significant Anti-TPO Positivity in Children with HLA-Conferred Susceptibility to Type 1 Diabetes
aUniversity of Tartu, Tartu, Estonia; bTartu University Hospital, Children’s Clinic, Tartu, Estonia
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Encephalopathy Associated with Autoimmune Thyroid Disease: A Case Report
University of Texas Health Science Center at Houston, Houston, USA
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A Successful Switch Experience from High-dose PTU to MMI on Day 4 of Graves' Thyroid Storm in a 14-Year-Old Girl
aIbaraki Seinan Medical Center Hospital, Department of Pediatrics, Tsukuba, Japan; bUniversity of Tsukuba, Faculty of Medicine, Department of Pediatrics, Tsukuba, Japan
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Phenotype and Genotype of Four Patients with Thyroid Hormone Resistance Syndrome due to Mutations in the THRB Gene
aPediatric Endocrine Clinic, IASIS Hospital, Paphos, Cyprus; bDepartment of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus; cDivision of Pediatric Endocrinology, Paedi Center for specialized Pediatrics, Nicosia, Cyprus; dSt George’s, University of London Medical School at the University of Nicosia, Nicosia, Cyprus; eCyprus School of Molecular Medicine, Nicosia, Cyprus; fDepartment of Clinical Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus; gLarnaca Endocrinology Center, Larnaca, Cyprus; hAlithias Endocrinology Center, Nicosia, Cyprus
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Clinical Course in a Girl with Two hTPO Mutations - Homozygous c.1268G>A (p.Gly393Arg) and Heterozygous c.208C>G (p.Ala70Pro): 27 Years of Follow Up
aUniversity Pediatric Hospital ‘Prof. Ivan Mitev’, Medical University, Sofia, Bulgaria; bMolecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria; cFirst Diagnostic and Consultation Center, Stara Zagora, Bulgaria; dGroup Practice for primary outpatient care ‘Medica MM’, Stara Zagora, Bulgaria
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A Neurological Disease Mimicking Central Hypothyroidism: MCT8 Deficiency
Department of Pediatrics, Division of Pediatric Endocrinology, Uludag University Faculty of Medicine, Bursa, Turkey
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Multinodular Goiter in Childhood: Look for DICER1 Mutation
aPediatric Endocrinology, Angers, France; bPediatric Endocrinology, Le Mans, France; cEndocrinology, Angers, France
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Application of Elastography in Assesment of Different Benign Thyroid Lesions in Children and Adolescents
aDepartment of Pediatrics, Endocinology, Diabetology with Cardiology Division, Medical University of Białystok, Białystok, Poland; bDepartment of Human Anatomy, Medical University of Białystok, Białystok, Poland; cStudent Research Group in Department of Pediatrics, Endocinology, Diabetology with Cardiology Division, Medical University of Białystok, Białystok, Poland
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Clinical Characteristics and Predictive Factors for the Detection of Thyroid Cancer in Children with Thyroid Nodules
Severance Children’s Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea
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Thyroid Nodules in Prader-Willi Syndrome
aItalian Auxological Institute, Verbania, Italy; bBambino Gesù Children’s Hospital, Rome, Italy
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Serum Level of Biotin Rather than the Daily Dose is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency
aDokuz Eylül University, Pediatric Endocrinology, izmir, Turkey; bDokuz Eylül University, Pediatric Metabolism and Nutrition, izmir, Turkey; cDokuz Eylül University, Biochemistry, izmir, Turkey
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Thyroid Function Tests and Affecting Factors in Twins and Triplets
aIstanbul Medipol University, Istanbul, Turkey; bAcibadem Mehmet Ali Aydinlar University, Istanbul, Turkey; cKosuyolu Medipol Hospital, Istanbul, Turkey
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Hypothyroidism in a Child During Treatment with Nivolumab for a Glioblastoma
Department of Pediatrics, Aarhus University Hospital, Aarhus, Denmark
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Diagnosis and Clinical Course of Amiodarone Induced Hyperthyroidism in Three Adolescent Patients
aHospital for Children and Adolescents University Hospital Leipzig, Leipzig, Germany; bHospital for Children and Adolescents University Hospital Schleswig-Holstein, Lübeck, Germany; cHeart Center Leipzig, Leipzig, Germany
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Allogenic Bone Marrow Transplantation in Children: Effect on Thyroid Function
aDepartment of Endocrinology-Growth and Development, Children’s Hosp. P. & A. Kyriakou, Athens, Greece; bAgia Sofia Children’s Hospital Stem Cell Transplantation Unit, Athens, Greece; cDepartment of Biochemitry, Children’s Hospital P. & A. Kyriakou, Athens, Greece
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Follow-up in Children with Non-obese and Non-autoimmune Subclinical Hypothyroidism
aHealth Sciences University, Dr Sami Ulus Obstetrics and Gynecology, Children’s Health and Disease, Health Implementation and Research Center, Pediatrics, Ankara, Turkey; bHealth Sciences University, Dr Sami Ulus Obstetrics and Gynecology, Children’s Health and Disease, Health Implementation and Research Center, Pediatric Endocrinology, Ankara, Turkey
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Clinical Management of Childhood Hyperthyroidism: A Longitudinal Study at a Single Center
aDepartments of Pediatrics & Pediatric Endocrinology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain; bLa Princesa Research Institute, Madrid, Spain; cCentro de Investigación Biomédica en Red de Fisiopatologia de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain; dUniversidad Autónoma de Madrid, Department of Pediatrics, Madrid, Spain; eUniversidad Autónoma de Madrid, Department of Preventive Medicine, Madrid, Spain; fIMDEA Food Institute, Madrid, Spain
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Association of Thyroid Stimulating Hormone and Free Thyroxine with Cardiometabolic Risk Factors in Euthyroid Korean children and Adolescents Aged 10-18 Years: The Korean National Health and Nutrition Examination Survey 2015
aDepartment of Pediatrics, Korea Cancer Center Hospital, Seoul, Korea, Seoul, Republic of Korea; bDepartment of Pediatrics, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea; cDepartment of Pediatrics, Chosun University School of Medicine, Gwangju, Republic of Korea
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Asymptomatic Hyperthyrotropinaemia in Children, Does it Correlate to true Thyroid Gland Dysfunction?
aGeneral Hospital of Nikaia, ‘Agios Panteleimon’, Athens, Greece; bMedical School, Aristotle University, Thessaloniki, Greece; c2nd Academic Paediatric Department, University General Hospital of Thessaloniki AHEPA, Thessaloniki, Greece
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Hearing Loss Among Patients with Congenital Hypothyroidism
aPediatric Endocrine Institute, Ha’Emek Medical Center, Afula, Israel; bPediatric Department B, Ha’Emek Medical Center, Afula, Israel; cDepartment of Otolaryngology, Head and Neck Surgery, Ha’Emek Medical Center, Afula, Israel; dClalit Health Organization, North District, Israel; eThe Rappaport Faculty of Medicine, Technion, Haifa, Israel
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Predictors of Permanent Congenital Hypothyroidism in Children
aPusan National University Children’s Hospital, Yangsan, Republic of Korea; bGyeongsang National University Changwon Hospital, Changwon, Republic of Korea
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Absence of Uptake on Scintigraphy Does Not Always Correlate with Athyreosis: Re-evaluation of Patients Diagnosed with Athyreosis Over a 10 Year Period in the Republic of Ireland
aDepartment of Paediatric Endocrinology, Children’s University Hospital, Temple St, Dublin, Ireland; bDepaetment of Paediatrics, University College Dublin, Dublin, Ireland; cDivision of Endocrinology and Diabetes, The Children’s Hospital of Philadelphia, Philadelphia, USA; dDepartment of Paediatric Radiology, Children’s University Hospital, Temple St, Dublin, Ireland
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Bannayan-Riley-Ruvalcaba Syndrome with PTEN Mutation in a Patient Affected by Congenital Hypothyroidism due to TPO Gene Alteration
aVita-Salute San Raffaele University, IRCSS San Raffele, Department of Pediatrics, Milan, Italy; bVita-Salute San Raffaele University, IRCSS San Raffele, Department of Radiology, Milan, Italy; cVita-Salute San Raffaele University, IRCSS San Raffele, Department of Endocrine Surgery, Milan, Italy; dVita-Salute San Raffaele University, IRCSS San Raffele, Medical Genetics Unit, Milan, Italy; eVita-Salute San Raffaele University, IRCSS San Raffele, Department of Pediatrics, Milan, Italy
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The Congenital Hypothyroidism Screening Programme in a Sigle Italian Centre: a 5-Years Retrospective Study
aUniversity Department Pro.Sa.M.I. ‘G. D’Alessandro’, University of Palermo, Italy, Palermo, Italy; bU.O.S. Screening Neonatale e Metabolico Allargato of the Children Hospital ‘G. Di Cristina’, ARNAS, Palermo, Palermo, Italy
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Study of Hearing Function in Children with Congenital Hypothyroidism Attending Alexandria University Children's Hospital
aFaculty of Medicine, Pediatric Endocrinology and Diabetology Unit, Alexandria University Children’s Hospital, Alexandria, Egypt; bFaculty of Medicine, Otorhinolaryngeology, Audiology, Alexandria University, Alexandria, Egypt; cPediatric Endocrinology and Diabetology Unit, Alexandria University Children’s Hospital, Alexandria, Egypt
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Awareness of the Risks of Acquired Iodine Deficiency in Strict Vegan Diets
aEvelina London Children’s Hospital, London, UK; bMedical University of Gdansk, Gdansk, Poland
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