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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: davie mw. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306. doi: 10.1111/j.1365-2265.2006.02460.x. Clin Endocrinol (Oxf). 2006. PMID: 16487440
Identifying coeliac disease in DXA referrals.
Davie MW. Davie MW. Osteoporos Int. 2014 Sep;25(9):2329. doi: 10.1007/s00198-014-2771-9. Epub 2014 Jun 28. Osteoporos Int. 2014. PMID: 24972587 No abstract available.
91 results