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Molecular basis of Bernard-Soulier syndrome in 27 patients from India.
Sumitha E, Jayandharan GR, David S, Jacob RR, Sankari Devi G, Bargavi B, Shenbagapriya S, Nair SC, Abraham A, George B, Viswabandya A, Mathews V, Chandy M, Srivastava A. Sumitha E, et al. Among authors: viswabandya a. J Thromb Haemost. 2011 Aug;9(8):1590-8. doi: 10.1111/j.1538-7836.2011.04417.x. J Thromb Haemost. 2011. PMID: 21699652 Free article.
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: viswabandya a. 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: viswabandya a. Semin Thromb Hemost. 2005 Nov;31(5):538-43. doi: 10.1055/s-2005-922225. Semin Thromb Hemost. 2005. PMID: 16276462 Review.
203 results