Srivastava A - Search Results

1

Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India.

Jayandharan G, Shaji RV, George B, Chandy M, Srivastava A. Jayandharan G, et al. Among authors: srivastava a. Haemophilia. 2004 Sep;10(5):553-9. doi: 10.1111/j.1365-2516.2004.00908.x. Haemophilia. 2004. PMID: 15357783

2

Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.

Jayandharan G, Shaji RV, Baidya S, Nair SC, Chandy M, Srivastava A. Jayandharan G, et al. Among authors: srivastava a. Haemophilia. 2005 Sep;11(5):481-91. doi: 10.1111/j.1365-2516.2005.01121.x. Haemophilia. 2005. PMID: 16128892

3

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

Peyvandi F, Jayandharan G, Chandy M, Srivastava A, Nakaya SM, Johnson MJ, Thompson AR, Goodeve A, Garagiola I, Lavoretano S, Menegatti M, Palla R, Spreafico M, Tagliabue L, Asselta R, Duga S, Mannucci PM. Peyvandi F, et al. Among authors: srivastava a. Haemophilia. 2006 Jul;12 Suppl 3:82-9. doi: 10.1111/j.1365-2516.2006.01263.x. Haemophilia. 2006. PMID: 16684001 Review.

4

Fracture neck of femur in haemophilia A - experience from a cohort of 11 patients from a tertiary centre in India.

Lee VN, Srivastava A, Nithyananth M, Kumar P, Cherian VM, Viswabandya A, Mathews V, George B, Venkatesh K, Nair SC, Chandy M, Sundararaj GD. Lee VN, et al. Among authors: srivastava a. Haemophilia. 2007 Jul;13(4):391-4. doi: 10.1111/j.1365-2516.2007.01448.x. Haemophilia. 2007. PMID: 17610554

5

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.

Jayandharan G, Spreafico M, Viswabandya A, Chandy M, Srivastava A, Peyvandi F. Jayandharan G, et al. Among authors: srivastava a. Haemophilia. 2007 Jul;13(4):413-9. doi: 10.1111/j.1365-2516.2007.01477.x. Haemophilia. 2007. PMID: 17610559

6

Successful surgical haemostasis in patients with von Willebrand disease with Koate DVI.

Viswabandya A, Mathews V, George B, Nair SC, Baidya S, Mammen JJ, Chandy M, Srivastava A. Viswabandya A, et al. Among authors: srivastava a. Haemophilia. 2008 Jul;14(4):763-7. doi: 10.1111/j.1365-2516.2008.01755.x. Epub 2008 Apr 24. Haemophilia. 2008. PMID: 18445014 Clinical Trial.

7

Polymorphism in factor VII gene modifies phenotype of severe haemophilia.

Jayandharan GR, Nair SC, Poonnoose PM, Thomas R, John J, Keshav SK, Cherian RS, Devadarishini M, Lakshmi KM, Shaji RV, Viswabandya A, George B, Mathews V, Chandy M, Srivastava A. Jayandharan GR, et al. Among authors: srivastava a. Haemophilia. 2009 Nov;15(6):1228-36. doi: 10.1111/j.1365-2516.2009.02080.x. Epub 2009 Aug 16. Haemophilia. 2009. PMID: 19686262

8

Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India.

Viswabandya A, Baidya S, Nair SC, Abraham A, George B, Mathews V, Chandy M, Srivastava A. Viswabandya A, et al. Among authors: srivastava a. Haemophilia. 2012 May;18(3):e195-200. doi: 10.1111/j.1365-2516.2011.02730.x. Epub 2012 Jan 4. Haemophilia. 2012. PMID: 22221743

9

Molecular basis of quantitative fibrinogen disorders in 27 patients from India.

Sumitha E, Jayandharan GR, Arora N, Abraham A, David S, Devi GS, Shenbagapriya P, Nair SC, George B, Mathews V, Chandy M, Viswabandya A, Srivastava A. Sumitha E, et al. Among authors: srivastava a. Haemophilia. 2013 Jul;19(4):611-8. doi: 10.1111/hae.12143. Epub 2013 Apr 8. Haemophilia. 2013. PMID: 23560673

10

Fluorescent PCR-based gene dose analysis for detection of deletion mutations in carriers of haemophilia.

Devi GS, Arora N, Rajkumar SV, Edison ES, Srivastava A, Jayandharan GR. Devi GS, et al. Among authors: srivastava a. Haemophilia. 2013 Nov;19(6):e377-80. doi: 10.1111/hae.12233. Epub 2013 Jul 16. Haemophilia. 2013. PMID: 23855319 No abstract available.

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