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Bijayeswar Vaidya

Department of Diabetes

Endocrinology and Vascular Medicine

Peninsula Medical School

Royal Devon and Exeter Hospital

UK

[email]@hgmp.mrc.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Diabetes, Endocrinology and Vascular Medicine, Peninsula Medical School, Royal Devon and Exeter Hospital, UK. 2004
  • Institute of Biomedical and Clinical Science, Peninsula Medical School, Exeter, UK. 2004
  • Department of Medicine (Endocrinology), University of Newcastle upon Tyne, United Kingdom. 1999 - 2003
  • Department of Medicine, The James Cook University Hospital, Middlesbrough TS4 3BW, UK. 2002
  • Department of Endocrinology, School of Clinical Medical Sciences, University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom. 2000

References

  1. The emerging role of the CTLA-4 gene in autoimmune endocrinopathies. Vaidya, B., Pearce, S. Eur. J. Endocrinol. (2004) [Pubmed]
  2. Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation. Vaidya, B., Campbell, V., Tripp, J.H., Spyer, G., Hattersley, A.T., Ellard, S. Clin. Endocrinol. (Oxf) (2004) [Pubmed]
  3. 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, E.J., Imrie, H., Dickinson, A.J., Perros, P., Kendall-Taylor, P., Pearce, S.H. Clin. Endocrinol. (Oxf) (2003) [Pubmed]
  4. A race to the lab. Vaidya, B., Chan, K., Drury, J., Connolly, V. Lancet (2002) [Pubmed]
  5. Evidence for a new Graves disease susceptibility locus at chromosome 18q21. Vaidya, B., Imrie, H., Perros, P., Young, E.T., Kelly, W.F., Carr, D., Large, D.M., Toft, A.D., Kendall-Taylor, P., Pearce, S.H. Am. J. Hum. Genet. (2000) [Pubmed]
  6. Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure. Vaidya, B., Pearce, S., Kendall-Taylor, P. Clin. Endocrinol. (Oxf) (2000) [Pubmed]
  7. Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one family. Vaidya, B., Coffey, R., Coyle, B., Trembath, R., San Lazaro, C., Reardon, W., Kendall-Taylor, P. J. Clin. Endocrinol. Metab. (1999) [Pubmed]
 
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