Cheetham TD - Search Results

1

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: cheetham td. 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.

2

A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.

Pearce SH, Cheetham T, Imrie H, Vaidya B, Barnes ND, Bilous RW, Carr D, Meeran K, Shaw NJ, Smith CS, Toft AD, Williams G, Kendall-Taylor P. Pearce SH, et al. Am J Hum Genet. 1998 Dec;63(6):1675-84. doi: 10.1086/302145. Am J Hum Genet. 1998. PMID: 9837820 Free PMC article.

3

Autoimmune polyendocrinopathy syndrome type 1: treat with kid gloves.

Pearce SH, Cheetham TD. Pearce SH, et al. Among authors: cheetham td. Clin Endocrinol (Oxf). 2001 Apr;54(4):433-5. doi: 10.1046/j.1365-2265.2001.01250.x. Clin Endocrinol (Oxf). 2001. PMID: 11318777 Review. No abstract available.

4

The investigation of hypocalcaemia and rickets.

Singh J, Moghal N, Pearce SH, Cheetham T. Singh J, et al. Arch Dis Child. 2003 May;88(5):403-7. doi: 10.1136/adc.88.5.403. Arch Dis Child. 2003. PMID: 12716711 Free PMC article. Review.

5

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: cheetham td. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

6

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: cheetham td. J Mol Endocrinol. 2006 Aug;37(1):97-104. doi: 10.1677/jme.1.02072. J Mol Endocrinol. 2006. PMID: 16901927

7

The role of the IDDM2 locus in the susceptibility of UK APS1 subjects to type 1 diabetes mellitus.

Adamson KA, Cheetham TD, Kendall-Taylor P, Seckl JR, Pearce SH. Adamson KA, et al. Among authors: cheetham td. Int J Immunogenet. 2007 Feb;34(1):17-21. doi: 10.1111/j.1744-313X.2006.00643.x. Int J Immunogenet. 2007. PMID: 17284223 Free article.

8

Discordance for X-linked hypophosphataemic rickets in identical twin girls.

Owen CJ, Habeb A, Pearce SH, Wright M, Ichikawa S, Sorenson AH, Econs MJ, Cheetham TD. Owen CJ, et al. Among authors: cheetham td. Horm Res. 2009;71(4):237-44. doi: 10.1159/000201113. Epub 2009 Mar 4. Horm Res. 2009. PMID: 19258716

9

Diagnosis and management of polyendocrinopathy syndromes.

Owen CJ, Cheetham TD. Owen CJ, et al. Among authors: cheetham td. Endocrinol Metab Clin North Am. 2009 Jun;38(2):419-36, x. doi: 10.1016/j.ecl.2009.01.007. Endocrinol Metab Clin North Am. 2009. PMID: 19328420 Review.

10

Diagnosis and management of vitamin D deficiency.

Pearce SH, Cheetham TD. Pearce SH, et al. Among authors: cheetham td. BMJ. 2010 Jan 11;340:b5664. doi: 10.1136/bmj.b5664. BMJ. 2010. PMID: 20064851 Review. No abstract available.

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