Pearce SH - Search Results

1

Spontaneous and tetracosactide-induced anti-ACTH antibodies in man.

Gan EH, MacArthur K, Mitchell AL, Joshi A, Crock P, Pearce SH. Gan EH, et al. Among authors: pearce sh. Clin Endocrinol (Oxf). 2016 Apr;84(4):489-95. doi: 10.1111/cen.12795. Epub 2015 Jun 25. Clin Endocrinol (Oxf). 2016. PMID: 25880719 Free PMC article.

2

CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism.

Vaidya B, Oakes EJ, Imrie H, Dickinson AJ, Perros P, Kendall-Taylor P, Pearce SH. Vaidya B, et al. Among authors: pearce sh. Clin Endocrinol (Oxf). 2003 Jun;58(6):732-5. doi: 10.1046/j.1365-2265.2003.01778.x. Clin Endocrinol (Oxf). 2003. PMID: 12780750

3

Spontaneous reporting of adverse reactions to carbimazole and propylthiouracil in the UK.

Pearce SH. Pearce SH. Clin Endocrinol (Oxf). 2004 Nov;61(5):589-94. doi: 10.1111/j.1365-2265.2004.02135.x. Clin Endocrinol (Oxf). 2004. PMID: 15521961

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

No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. Among authors: pearce sh. Clin Endocrinol (Oxf). 2005 Mar;62(3):362-5. doi: 10.1111/j.1365-2265.2005.02224.x. Clin Endocrinol (Oxf). 2005. PMID: 15730420

6

A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. Among authors: pearce sh. J Mol Endocrinol. 2005 Jun;34(3):859-63. doi: 10.1677/jme.1.01760. J Mol Endocrinol. 2005. PMID: 15956353

7

What is the evidence behind the evidence-base? The premature death of block-replace antithyroid drug regimens for Graves' disease.

Razvi S, Vaidya B, Perros P, Pearce SH. Razvi S, et al. Among authors: pearce sh. Eur J Endocrinol. 2006 Jun;154(6):783-6. doi: 10.1530/eje.1.02169. Eur J Endocrinol. 2006. PMID: 16728536

8

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

Owen CJ, Eden JA, Jennings CE, Wilson V, Cheetham TD, Pearce SH. Owen CJ, et al. Among authors: pearce sh. J Mol Endocrinol. 2006 Aug;37(1):97-104. doi: 10.1677/jme.1.02072. J Mol Endocrinol. 2006. PMID: 16901927

9

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

10

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.

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