Authors:
Imrie, H
Vaidya, B
Perros, P
Kelly, WF
Toft, AD
Young, ET
Kendall-Taylor, P
Pearce, SHS
Citation: H. Imrie et al., Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population, J CLIN END, 86(2), 2001, pp. 626-630
Authors:
Scheinman, SJ
Cox, JPD
Lloyd, SE
Pearce, SHS
Salenger, PV
Hoopes, RR
Bushinsky, DA
Wrong, O
Asplin, JR
Langman, CB
Norden, AGW
Thakker, RV
Citation: Sj. Scheinman et al., Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria, KIDNEY INT, 57(1), 2000, pp. 232-239
Authors:
Vaidya, B
Imrie, H
Geatch, DR
Perros, P
Ball, SG
Baylis, PH
Carr, D
Hurel, SJ
James, RA
Kelly, WF
Kemp, EH
Young, ET
Weetman, AP
Kendall-Taylor, P
Pearce, SHS
Citation: B. Vaidya et al., Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease, J CLIN END, 85(2), 2000, pp. 688-691
Authors:
Vaidya, B
Imrie, H
Perros, P
Dickinson, J
McCarthy, MI
Kendall-Taylor, P
Pearce, SHS
Citation: B. Vaidya et al., Cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism confers susceptibility to thyroid associated orbitopathy, LANCET, 354(9180), 1999, pp. 743-744
Authors:
Pearce, SHS
Vaidya, B
Imrie, H
Perros, P
Kelly, WF
Toft, AD
McCarthy, MI
Young, ET
Kendall-Taylor, P
Citation: Shs. Pearce et al., Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease, AM J HU GEN, 65(5), 1999, pp. 1462-1465
Authors:
Kemp, EH
Ajjan, RA
Husebye, ES
Peterson, P
Uibo, R
Imrie, H
Pearce, SHS
Watson, PF
Weetman, AP
Citation: Eh. Kemp et al., A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients, CLIN ENDOCR, 49(5), 1998, pp. 609-613
Authors:
Pearce, SHS
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
Citation: Shs. Pearce et al., A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1, AM J HU GEN, 63(6), 1998, pp. 1675-1684