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Molecular IGF-1 and IGF-1 receptor defects: from genetics to clinical management.
Walenkamp MJ, Losekoot M, Wit JM. Walenkamp MJ, et al. Among authors: wit jm. Endocr Dev. 2013;24:128-37. doi: 10.1159/000342841. Epub 2013 Feb 1. Endocr Dev. 2013. PMID: 23392101 Review.
Characterization of an activating R1353H insulin-like growth factor 1 receptor variant in a male with extreme tall height.
Lin Y, van Duyvenvoorde HA, Liu H, Yang C, Warsito D, Yin C, Kant SG, Haglund F, Wit JM, Larsson O. Lin Y, et al. Among authors: wit jm. Eur J Endocrinol. 2018 Aug;179(2):85-95. doi: 10.1530/EJE-18-0176. Epub 2018 May 22. Eur J Endocrinol. 2018. PMID: 29789409
A Human Variant of Glucose-Regulated Protein 94 That Inefficiently Supports IGF Production.
Marzec M, Hawkes CP, Eletto D, Boyle S, Rosenfeld R, Hwa V, Wit JM, van Duyvenvoorde HA, Oostdijk W, Losekoot M, Pedersen O, Yeap BB, Flicker L, Barzilai N, Atzmon G, Grimberg A, Argon Y. Marzec M, et al. Among authors: wit jm. Endocrinology. 2016 May;157(5):1914-28. doi: 10.1210/en.2015-2058. Epub 2016 Mar 16. Endocrinology. 2016. PMID: 26982636 Free PMC article.
Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutation.
Vidarsdottir S, Walenkamp MJ, Pereira AM, Karperien M, van Doorn J, van Duyvenvoorde HA, White S, Breuning MH, Roelfsema F, Kruithof MF, van Dissel J, Janssen R, Wit JM, Romijn JA. Vidarsdottir S, et al. Among authors: wit jm. J Clin Endocrinol Metab. 2006 Sep;91(9):3482-5. doi: 10.1210/jc.2006-0368. Epub 2006 Jun 20. J Clin Endocrinol Metab. 2006. PMID: 16787985
STAT5b deficiency: lessons from STAT5b gene mutations.
Hwa V, Nadeau K, Wit JM, Rosenfeld RG. Hwa V, et al. Among authors: wit jm. Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):61-75. doi: 10.1016/j.beem.2010.09.003. Best Pract Res Clin Endocrinol Metab. 2011. PMID: 21396575 Review.
Spectrum of insulin-like growth factor deficiency.
Wit JM, Oostdijk W, Losekoot M. Wit JM, et al. Endocr Dev. 2012;23:30-41. doi: 10.1159/000341739. Epub 2012 Nov 23. Endocr Dev. 2012. PMID: 23182818 Review.
Genetic Analyses in Small-for-Gestational-Age Newborns.
Stalman SE, Solanky N, Ishida M, Alemán-Charlet C, Abu-Amero S, Alders M, Alvizi L, Baird W, Demetriou C, Henneman P, James C, Knegt LC, Leon LJ, Mannens MMAM, Mul AN, Nibbering NA, Peskett E, Rezwan FI, Ris-Stalpers C, van der Post JAM, Kamp GA, Plötz FB, Wit JM, Stanier P, Moore GE, Hennekam RC. Stalman SE, et al. Among authors: wit jm. J Clin Endocrinol Metab. 2018 Mar 1;103(3):917-925. doi: 10.1210/jc.2017-01843. J Clin Endocrinol Metab. 2018. PMID: 29342293
Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel IGFALS mutations.
Işık E, Haliloglu B, van Doorn J, Demirbilek H, Scheltinga SA, Losekoot M, Wit JM. Işık E, et al. Among authors: wit jm. Eur J Endocrinol. 2017 Jun;176(6):657-667. doi: 10.1530/EJE-16-0999. Epub 2017 Mar 1. Eur J Endocrinol. 2017. PMID: 28249955
Association between head circumference and body size.
Geraedts EJ, van Dommelen P, Caliebe J, Visser R, Ranke MB, van Buuren S, Wit JM, Oostdijk W. Geraedts EJ, et al. Among authors: wit jm. Horm Res Paediatr. 2011;75(3):213-9. doi: 10.1159/000321192. Epub 2011 Feb 10. Horm Res Paediatr. 2011. PMID: 21311161
Evaluation of asymptomatic short children.
Wit JM, Oostdijk W. Wit JM, et al. J Pediatr. 2013 Nov;163(5):1534-5. doi: 10.1016/j.jpeds.2013.07.037. Epub 2013 Sep 5. J Pediatr. 2013. PMID: 24011761 No abstract available.
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