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Pitfalls in the measurement and interpretation of thyroid function tests.
Koulouri O, Moran C, Halsall D, Chatterjee K, Gurnell M. Koulouri O, et al. Among authors: moran c. Best Pract Res Clin Endocrinol Metab. 2013 Dec;27(6):745-62. doi: 10.1016/j.beem.2013.10.003. Epub 2013 Oct 17. Best Pract Res Clin Endocrinol Metab. 2013. PMID: 24275187 Free PMC article. Review.
Familial dysalbuminemic hyperthyroxinemia: a persistent diagnostic challenge.
Cartwright D, O'Shea P, Rajanayagam O, Agostini M, Barker P, Moran C, Macchia E, Pinchera A, John R, Agha A, Ross HA, Chatterjee VK, Halsall DJ. Cartwright D, et al. Among authors: moran c. Clin Chem. 2009 May;55(5):1044-6. doi: 10.1373/clinchem.2008.120303. Epub 2009 Mar 12. Clin Chem. 2009. PMID: 19282355 No abstract available.
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.
Schoenmakers N, Moran C, Campi I, Agostini M, Bacon O, Rajanayagam O, Schwabe J, Bradbury S, Barrett T, Geoghegan F, Druce M, Beck-Peccoz P, O'Toole A, Clark P, Bignell M, Lyons G, Halsall D, Gurnell M, Chatterjee K. Schoenmakers N, et al. Among authors: moran c. J Clin Endocrinol Metab. 2014 Jul;99(7):E1381-6. doi: 10.1210/jc.2013-4077. Epub 2014 Mar 19. J Clin Endocrinol Metab. 2014. PMID: 24646103 Free PMC article.
Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients.
Moran C, Agostini M, Visser WE, Schoenmakers E, Schoenmakers N, Offiah AC, Poole K, Rajanayagam O, Lyons G, Halsall D, Gurnell M, Chrysis D, Efthymiadou A, Buchanan C, Aylwin S, Chatterjee KK. Moran C, et al. Lancet Diabetes Endocrinol. 2014 Aug;2(8):619-26. doi: 10.1016/S2213-8587(14)70111-1. Epub 2014 Jun 23. Lancet Diabetes Endocrinol. 2014. PMID: 24969835 Free PMC article.
2,150 results