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American Journal of Hematology|November 1, 1995
Two antithrombin mutations in a compound heterozygote: Met20Thr and Tyr166CysD J Perry, M E Daly, B T Colvin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2008
Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiencyN M O'Connell, A F Riddell, G Pascoe, et al.
The Journal of Clinical Investigation|December 1, 1994
Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn-->Asp)D Bruce, D J Perry, J Y Borg, et al.
British Journal of Haematology|July 19, 2006
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantationF Peyvandi, S M Siboni, D Lambertenghi Deliliers, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1997
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenariansP M Mannucci, D Mari, G Merati, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2013
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutationsM Borhany, H Handrkova, A Cairo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 26, 2014
Genetic testing in bleeding disordersC de Brasi, O El-Maarri, D J Perry, et al.
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