Schilddrüsenfunktionsstörungen in der Schwangerschaft
Dagmar Führer(West German Heart and Vascular Center Essen), M. Schott, Jürgen Kratzsch(Leipzig University), K. Mann(Praxis), Joachim Feldkamp(Klinikum Bielefeld), Heiko Krude(Humboldt-Universität zu Berlin), Christine Spitzweg(Mayo Clinic)
Cited by 13
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
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
Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist
|New England Journal of Medicine|2016|480