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British Journal of Haematology|December 22, 1999
Heterozygous factor XI deficiency associated with three novel mutationsM Mitchell, J Cutler, S Thompson, et al.
Journal of Thrombosis and Haemostasis : JTH|December 23, 2004
The profibrinolytic effect of plasma thrombomodulin in factor XI deficiency and its implications in hemostasisL Dai, M Mitchell, G Savidge, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Real-time quantitative PCR analysis of factor XI mRNA variants in human plateletsA Podmore, M Smith, G Savidge, et al.
British Journal of Haematology|February 23, 1999
Identification of a novel mutation in a non-Jewish factor XI deficient kindredA Alhaq, M Mitchell, M Sethi, et al.
Clinical and Laboratory Haematology|January 24, 2004
Validation of a quantitative SPR assay for recombinant FVIIIA N McCormick, M E Leach, G Savidge, et al.
Clinical and Laboratory Haematology|November 28, 2002
Evaluation of an automated screening assay for von Willebrand disease type 2NS L Taylor, E Bromidge, G F Savidge, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1979
Serum T3 and T4 determinations during the TRH test as a complement to improved discriminatory power in suspect hyperthyroidismJ G Ljunggren, G Kallner, G Savidge
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
A post-marketing safety and efficacy assessment of a monoclonal antibody purified high-purity factor VIII concentrateC R Hay, C A Lee, G Savidge
Journal of Clinical Pathology|February 1, 1988
Clinical application of new technique that measures C4d for assessment of activation of classical complement pathwayE T Davies, B A Nasaruddin, A Alhaq, et al.
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