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Page 1
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S. Farooqi IS, et al. N Engl J Med. 2007 Jan 18;356(3):237-47. doi: 10.1056/NEJMoa063988. N Engl J Med. 2007. PMID: 17229951 Free PMC article.
Cell proliferation activities on skin fibroblasts from a short child with absence of one copy of the type 1 insulin-like growth factor receptor (IGF1R) gene and a tall child with three copies of the IGF1R gene.
Okubo Y, Siddle K, Firth H, O'Rahilly S, Wilson LC, Willatt L, Fukushima T, Takahashi S, Petry CJ, Saukkonen T, Stanhope R, Dunger DB. Okubo Y, et al. J Clin Endocrinol Metab. 2003 Dec;88(12):5981-8. doi: 10.1210/jc.2002-021080. J Clin Endocrinol Metab. 2003. PMID: 14671200
Regarding the consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology.
Creighton S, Ransley P, Duffy P, Wilcox D, Mushtaq I, Cuckow P, Woodhouse C, Minto C, Crouch N, Stanhope R, Hughes I, Dattani M, Hindmarsh P, Brain C, Achermann J, Conway G, Liao LM, Barnicoat A, Perry L. Creighton S, et al. J Clin Endocrinol Metab. 2003 Jul;88(7):3455; author reply 3456. doi: 10.1210/jc.2003-030127. J Clin Endocrinol Metab. 2003. PMID: 12843205 No abstract available.
Investigation of delayed puberty.
Albanese A, Stanhope R. Albanese A, et al. Clin Endocrinol (Oxf). 1995 Jul;43(1):105-10. doi: 10.1111/j.1365-2265.1995.tb01899.x. Clin Endocrinol (Oxf). 1995. PMID: 7641400
Delayed puberty.
Traggiai C, Stanhope R. Traggiai C, et al. Best Pract Res Clin Endocrinol Metab. 2002 Mar;16(1):139-51. doi: 10.1053/beem.2001.0186. Best Pract Res Clin Endocrinol Metab. 2002. PMID: 11987904 Review.
199 results