Pearce SHS - Search Results

1

Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease.

Cheetham TD, Cole M, Abinun M, Allahabadia A, Barratt T, Davies JH, Dimitri P, Drake A, Mohamed Z, Murray RD, Steele CA, Zammitt N, Carnell S, Prichard J, Watson G, Hambleton S, Matthews JNS, Pearce SHS. Cheetham TD, et al. Among authors: pearce shs. J Clin Endocrinol Metab. 2022 Feb 17;107(3):743-754. doi: 10.1210/clinem/dgab763. J Clin Endocrinol Metab. 2022. PMID: 34687316 Free PMC article. Clinical Trial.

2

The genetics of autoimmune thyroid disease.

Vaidya B, Kendall-Taylor P, Pearce SH. Vaidya B, et al. 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

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.

4

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. Clin Endocrinol (Oxf). 2003 Jun;58(6):732-5. doi: 10.1046/j.1365-2265.2003.01778.x. Clin Endocrinol (Oxf). 2003. PMID: 12780750

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

6

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy.

Waller S, Kurzawinski T, Spitz L, Thakker R, Cranston T, Pearce S, Cheetham T, van't Hoff WG. Waller S, et al. Eur J Pediatr. 2004 Oct;163(10):589-94. doi: 10.1007/s00431-004-1491-0. Eur J Pediatr. 2004. PMID: 15241688

7

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

8

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. J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5. doi: 10.1210/jc.2004-1108. J Clin Endocrinol Metab. 2004. PMID: 15531553

9

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. Clin Endocrinol (Oxf). 2005 Mar;62(3):362-5. doi: 10.1111/j.1365-2265.2005.02224.x. Clin Endocrinol (Oxf). 2005. PMID: 15730420

10

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. Eur J Endocrinol. 2006 Jun;154(6):783-6. doi: 10.1530/eje.1.02169. Eur J Endocrinol. 2006. PMID: 16728536

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