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Journal of Thrombosis and Haemostasis : JTH|April 27, 2013
An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia BP M Rallapalli, G Kemball-Cook, E G Tuddenham, et al.Blood|April 1, 1997
A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasminS Pemberton, P Lindley, V Zaitsev, et al.Thrombosis and Haemostasis|May 9, 2001
Standardisation of factor VIII and von Willebrand factor in plasma: calibration of the 4th International Standard (97/586)A R Hubbard, P Rigsby, T W BarrowcliffeBritish Journal of Haematology|September 1, 1983
Studies of the heterogeneity of antithrombin III concentratesT W Barrowcliffe, C A Eggleton, M MahmoudHuman Mutation|January 4, 2001
Factor VII deficiency and the FVII mutation databaseJ H McVey, E Boswell, A D Mumford, et al.British Journal of Haematology|July 11, 2000
Assay discrepancy in mild haemophilia A due to a factor VIII missense mutation (Asn694Ile) in a large Danish familyR Schwaab, J Oldenburg, G Kemball-Cook, et al.Thrombosis and Haemostasis|December 1, 1996
Collaborative study on assays of activated FIX (FIXa). On behalf of the factor VIII and factor IX subcommittee of the ISTH. International Society on Thrombosis and HaemostasisE Gray, D Walker, A Heath, et al.Thrombosis and Haemostasis|February 29, 1980
An international collaborative study establishing a reference preparation for Antithrombin IIIT B Kirkwood, T W Barrowcliffe, D P ThomasThrombosis Research|September 1, 1984
Anticoagulant properties in vitro of heparan sulphatesA R Hubbard, C A Jennings, T W BarrowcliffeThrombosis and Haemostasis|September 1, 1993
Evaluation of factor VIII deficient plasmasT W Barrowcliffe, J E Tubbs, M Y WongPageof 14