C. Noordam

Hepatocyte nuclear factor‐1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF‐1β in human pancreatic development

Emma L. Edghill, Coralie Bingham, A. S. Slingerland et al. · Diabetic Medicine · 2006 · 175 citations

Medicine, Endocrinology, Genetics +16

Inactivating <i>PAPSS2</i> Mutations in a Patient with Premature Pubarche

C. Noordam, Vivek Dhir, Joanne McNelis et al. · New England Journal of Medicine · 2009 · 169 citations

Life Sciences, Endocrinology, Genetics +17

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by<i>TPIT</i>Gene Mutations

Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 126 citations · Full text

Medicine, Endocrinology, Genetics +17

Long-term GH treatment improves adult height in children with Noonan syndrome with and without mutations in protein tyrosine phosphatase, non-receptor-type 11

C. Noordam, P.G.M. Peer, Inge François et al. · European Journal of Endocrinology · 2008 · 93 citations

Medicine, Endocrinology, Pediatrics +15

Adult Height in Short Children Born SGA Treated with Growth Hormone and Gonadotropin Releasing Hormone Analog: Results of a Randomized, Dose-Response GH Trial

Annemieke J. Lem, Daniëlle C M van der Kaay, Maria de Ridder et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 92 citations · Full text

Medicine, Endocrinology, Pediatrics +17