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Page 1
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.
Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM, Conceição Pereira M, Davie MW, Dudley N, Leite V, Sadler GP, Seller A, Thakker RV. Bradley KJ, et al. Among authors: sadler gp. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306. doi: 10.1111/j.1365-2265.2006.02460.x. Clin Endocrinol (Oxf). 2006. PMID: 16487440
Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.
Newey PJ, Nesbit MA, Rimmer AJ, Attar M, Head RT, Christie PT, Gorvin CM, Stechman M, Gregory L, Mihai R, Sadler G, McVean G, Buck D, Thakker RV. Newey PJ, et al. J Clin Endocrinol Metab. 2012 Oct;97(10):E1995-2005. doi: 10.1210/jc.2012-2303. Epub 2012 Aug 1. J Clin Endocrinol Metab. 2012. PMID: 22855342 Free PMC article.
Confusing genes: a patient with MEN2A and Cushing's disease.
Naziat A, Karavitaki N, Thakker R, Ansorge O, Sadler G, Gleeson F, Cranston T, McCormack A, Grossman AB, Shine B. Naziat A, et al. Clin Endocrinol (Oxf). 2013 Jun;78(6):966-8. doi: 10.1111/cen.12072. Epub 2013 Apr 6. Clin Endocrinol (Oxf). 2013. PMID: 23072303 No abstract available.
Asymptomatic hyperparathyroidism--need for multicentre studies.
Mihai R, Wass JA, Sadler GP. Mihai R, et al. Among authors: sadler gp. Clin Endocrinol (Oxf). 2008 Feb;68(2):155-64. doi: 10.1111/j.1365-2265.2007.02970.x. Epub 2007 Jul 25. Clin Endocrinol (Oxf). 2008. PMID: 17651448 Review.
51 results