European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
Juliane Léger(Hôpital Robert-Debré), Gary Butler(Great Ormond Street Hospital), Antonella Olivieri(Istituto Superiore di Sanità), Malcolm Donaldson(University of Glasgow), Heiko Krude(Humboldt-Universität zu Berlin), Michel Polak(Hôpital Necker-Enfants Malades), Toni Torresani(University Children's Hospital Zurich), Guy Van Vliet(Centre Hospitalier Universitaire Sainte-Justine)
Cited by 205
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
|The Journal of Experimental Medicine|2010|721
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
|The Lancet|2004|707
European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
|The Journal of Clinical Endocrinology & Metabolism|2014|569
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|503