Normal Values for the fT3/fT4 Ratio: Centile Charts (0-29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay
Nina‐Maria Wilpert(Humboldt-Universität zu Berlin), Markus Schuelke(Humboldt-Universität zu Berlin), Dominik Seelow(Humboldt-Universität zu Berlin), Mandy Vogel(Leipzig University), Jürgen Kratzsch(Leipzig University), Heiko Krude(Humboldt-Universität zu Berlin), Michael Thamm(Robert Koch Institute)
Cited by 2
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
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
|Nature Genetics|2006|567
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|503