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Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin.
Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, George B, Chandy M, Srivastava A. Jayandharan G, et al. Among authors: baidya s. J Thromb Haemost. 2005 Jul;3(7):1482-7. doi: 10.1111/j.1538-7836.2005.01339.x. Epub 2005 May 9. J Thromb Haemost. 2005. PMID: 15892863 Free article.
Surgery for hemophilia in developing countries.
Mathews V, Viswabandya A, Baidya S, George B, Nair S, Chandy M, Srivastava A. Mathews V, et al. Among authors: baidya s. Semin Thromb Hemost. 2005 Nov;31(5):538-43. doi: 10.1055/s-2005-922225. Semin Thromb Hemost. 2005. PMID: 16276462 Review.
143 results