Items where Author is "Baidya, S. "

Article

Viswabandya, A. ; Baidya, S. ; Nair, S. C. ; Abraham, A. ; George, B. ; Mathews, V. ; Chandy, M. ; Srivastava, A. (2012) Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India Haemophilia, 18 (3). pp. e195-e200. ISSN 1351-8216

Viswabandya, A. ; Mathews, V. ; George, B. ; Nair, S. C. ; Baidya, S. ; Mammen, J. J. ; Chandy, M. ; Srivastava, A. (2008) Successful surgical haemostasis in patients with von willebrand disease with koate DVI Haemophilia, 14 (4). pp. 763-767. ISSN 1351-8216

Jayandharan, G. ; Nelson, E. J. R. ; Baidya, S. ; Chandy, M. ; Srivastava, A. (2007) A new multiplex PCR and conformation-sensitive gel electrophoresis strategy for mutation detection in the platelet glycoprotein αIIb and β3 genes Journal of Thrombosis and Haemostasis, 5 (1). pp. 206-209. ISSN 1538-7933

Jayandharan, G. ; Shaji, R. V. ; Baidya, S. ; Nair, S. C. ; Chandy, M. ; Srivastava, A. (2005) 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 Haemophilia, 11 (5). pp. 481-491. ISSN 1351-8216

Jayandharan, G. ; Viswabandya, A. ; Baidya, S. ; Nair, S. C. ; Shaji, R. V. ; Chandy, M. ; Srivastava, A. (2005) Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362→Thr (Prothrombin Vellore 1) mutation Journal of Thrombosis and Haemostasis, 3 (7). pp. 1446-1453. ISSN 1538-7933

Jayandharan, G. ; Viswabandya, A. ; Baidya, S. ; nair, S. C. ; shaji, R. V. ; George, B. ; Chandy, M. ; Srivastava, A. (2005) 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 Journal of Thrombosis and Haemostasis, 3 (7). pp. 1482-1487. ISSN 1538-7933

Shaji, R. V. ; Eunice, S. E. ; Baidya, S. ; Srivastava, A. ; Chandy, M. (2003) Determination of the breakpoint and molecular diagnosis of a common α-thalassaemia-1 deletion in the Indian population British Journal of Haematology, 123 (5). pp. 942-947. ISSN 0007-1048