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Hormone Research in Paediatrics|April 29, 2010
Adult height in children with growth hormone deficiency: a randomized, controlled, growth hormone dose-response trialTheo C J Sas, Maria A J de Ridder, Jan M Wit, et al.
Hormone Research in Paediatrics|October 27, 2021
Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1Joel Riquelme, Sanami Takada, Tessa van Dijk, et al.
The Journal of Pediatrics|January 13, 2005
Growth hormone (GH) treatment to final height in children with idiopathic short stature: evidence for a dose effectJan M Wit, Lyset T M Rekers-Mombarg, Gordon B Cutler, et al.
European Journal of Endocrinology|June 3, 2015
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritabilityRenata C Scalco, Vivian Hwa, Horacio M Domené, et al.
Hormone Research in Paediatrics|March 2, 2010
Marginal growth increase, altered bone quality and polycystic ovaries in female prepubertal rats after treatment with the aromatase inhibitor exemestaneSandy A van Gool, Jan M Wit, Tineke De Schutter, et al.
Hormone Research in Paediatrics|December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short statureEva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
The Journal of Clinical Endocrinology and Metabolism|March 9, 2019
Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 ReceptorMarie J E Walenkamp, Jasmijn M L Robers, Jan M Wit, et al.
Hormone Research in Paediatrics|April 15, 2010
Impaired body weight and tail length gain and altered bone quality after treatment with the aromatase inhibitor exemestane in male ratsSandy A van Gool, Jan M Wit, Tineke De Schutter, et al.
Fertility and Sterility|September 13, 2015
Mid-pregnancy, perinatal, and neonatal reproductive endocrinology: a prospective cohort study in twins and singleton control subjectsEsther A M Kuijper, Jos W R Twisk, Ted Korsen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 30, 2009
Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotypeWietske A Ester, Hermine A van Duyvenvoorde, Caroline C de Wit, et al.
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