Pearce SH - Search Results

1

Clinical review: The thyroid in mind: cognitive function and low thyrotropin in older people.

Gan EH, Pearce SH. Gan EH, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2012 Oct;97(10):3438-49. doi: 10.1210/jc.2012-2284. Epub 2012 Aug 3. J Clin Endocrinol Metab. 2012. PMID: 22865905 Free PMC article. Review.

2

The genetics of autoimmune thyroid disease.

Vaidya B, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2002 Dec;87(12):5385-97. doi: 10.1210/jc.2002-020492. J Clin Endocrinol Metab. 2002. PMID: 12466323 Review. No abstract available.

3

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.

Owen CJ, Jennings CE, Imrie H, Lachaux A, Bridges NA, Cheetham TD, Pearce SH. Owen CJ, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

4

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH. Velaga MR, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5. doi: 10.1210/jc.2004-1108. J Clin Endocrinol Metab. 2004. PMID: 15531553

5

Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association.

Owen CJ, Kelly H, Eden JA, Merriman ME, Pearce SH, Merriman TR. Owen CJ, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2007 Mar;92(3):1106-11. doi: 10.1210/jc.2006-2183. Epub 2007 Jan 2. J Clin Endocrinol Metab. 2007. PMID: 17200162

6

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.

Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH. Sutherland A, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2007 Aug;92(8):3338-41. doi: 10.1210/jc.2007-0173. Epub 2007 May 29. J Clin Endocrinol Metab. 2007. PMID: 17535987 Free PMC article.

7

How should we treat patients with low serum thyrotropin concentrations?

Mitchell AL, Pearce SH. Mitchell AL, et al. Among authors: pearce sh. Clin Endocrinol (Oxf). 2010 Mar;72(3):292-6. doi: 10.1111/j.1365-2265.2009.03694.x. Epub 2009 Sep 10. Clin Endocrinol (Oxf). 2010. PMID: 19744106 Review.

8

Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility.

Mitchell AL, Cordell HJ, Soemedi R, Owen K, Skinningsrud B, Wolff AB, Ericksen M, Undlien D, Husebye E, Pearce SH. Mitchell AL, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2009 Dec;94(12):5139-45. doi: 10.1210/jc.2009-1404. Epub 2009 Oct 22. J Clin Endocrinol Metab. 2009. PMID: 19850680

9

The incidence of ischemic heart disease and mortality in people with subclinical hypothyroidism: reanalysis of the Whickham Survey cohort.

Razvi S, Weaver JU, Vanderpump MP, Pearce SH. Razvi S, et al. Among authors: pearce sh. J Clin Endocrinol Metab. 2010 Apr;95(4):1734-40. doi: 10.1210/jc.2009-1749. Epub 2010 Feb 11. J Clin Endocrinol Metab. 2010. PMID: 20150579

10

The role of a nonsynonymous CD226 (DNAX-accessory molecule-1) variant (Gly 307Ser) in isolated Addison's disease and autoimmune polyendocrinopathy type 2 pathogenesis.

Gan EH, Mitchell AL, Macarthur K, Pearce SH. Gan EH, et al. Among authors: pearce sh. Clin Endocrinol (Oxf). 2011 Aug;75(2):165-8. doi: 10.1111/j.1365-2265.2011.04030.x. Clin Endocrinol (Oxf). 2011. PMID: 21521299

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