Previous issue | Volume 92 | ESPE2019

58th Annual ESPE meeting

Vienna, Austria
19 Sep 2019 - 21 Sep 2019

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The theme of this year’s meeting is Variety and Variation in Paediatric Endocrinology. Join us in Vienna to explore the diversity we encounter in our discipline and the care that we have to exercise when using the term “normality”. Whilst gaining an update on the latest treatments, clinical best practice and cutting edge research in the field of paediatric endocrinology.

Rapid Free Communications

Thyroid

Hurthle Cell Carcinoma in Childhood: Retrospective Analysis of a Large Series
1Department of Human Pathology of Adulthood and Childhood, University of Messina, Messina, Italy. 2Department of Pediatrics, Regina Margherita Children's Hospital, Turin, Italy
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Ultrasound Features of Multinodular Goiter in DICER1 Syndrome
1Department of Pediatric Endocrinology and Rheumatology, Karol Jonscher's Clinical Hospital, Poznan University of Medical Sciences, Poznan, Poland. 2Department of Radiology, Montreal Children's Hospital, McGill University Health Centre, Montreal, Canada. 3Department of Human Genetics, Montreal, Canada. 4Department of Medical Genetics, McGill University Health Centre, Montreal, Canada. 5Lady Davis Institute, Jewish General Hospital, Montreal, Canada
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Thyroid Dysfunction in Patients Following Thymus Transplantation in a Tertiary Centre: A 10-Year Experience
1Department of Paediatric Endocrinology, Great Ormond Street Hospital, London, London, United Kingdom. 2Department of Paediatric Immunology, Great Ormond Street Hospital, London, London, United Kingdom
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A Novel Mutation in the Thyroglobulin Gene Leading to Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant
1Pediatric Endocrine and Diabetes Unit, Sheba Medical Center, Edmond and Lily Safra Children's Hospital, Ramat Gan, Israel. 2Department of Obstetrics and Gynecology, Sheba Medical Center, Tel-Hashomer, Ramat Gan, Israel. 3University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital and National Institute for Health Research Cambridge Biomedical Research Centre, Addenbrooke's Hospital, Cambridge, United Kingdom. 4Pediatric Endocrine and Diabetes Unit, Assuta Medical Center, Ashdod, Israel
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Complex Single Nucleotide Polymorphisms in SEPINA 7 Lead to TBG Deficiency
11st affliated hospital of zhejiang university school of medicine, Hangzhou, China. 2zhejiang university school of medicine, Hangzhou, China
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