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British Journal of Haematology
|
February 1, 1980
An agarose plate method for detecting alloantisera to coagulant factor IX and factor IX antigen
H M Reisner, E A Strand, K S Chung, et al.
British Journal of Haematology
|
June 1, 1970
Continuous intravenous infusion of factor VIII in classic haemophilia
C W McMillan, W P Webster, H R Roberts, et al.
Archives of Internal Medicine
|
September 1, 1976
Hemolysis caused by factor VIII concentrates
E P Orringer, M J Koury, P M Blatt, et al.
Blood
|
October 1, 1980
Detection of factor IX antibodies by radioimmunoassay: effect of calcium on antibody-factor IX interaction
R M Lewis, H M Reisner, K S Chung, et al.
Blood
|
September 1, 1985
Comparison of inhibitory and binding characteristics of an antibody causing acquired von Willebrand syndrome: an assay for von Willebrand factor binding by antibody
W A Fricke, K M Brinkhous, J B Garris, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 14, 2001
Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic procedures
H A Cooper, C P Jones, E Campion, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 17, 2005
Cellular immune responses in hemophilia: why do inhibitors develop in some, but not all hemophiliacs?
G C White, C L Kempton, A Grimsley, et al.
Thrombosis and Haemostasis
|
October 31, 1979
Detection of an abnormal plasma clot structure by a simple rigidity assay
M E Carr, P M Blatt, H R Roberts, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 5, 1999
Newer concepts of blood coagulation
H R Roberts, D M Monroe, J A Oliver, et al.
British Journal of Haematology
|
July 27, 2001
High-dose factor VIIa increases initial thrombin generation and mediates faster platelet activation in thrombocytopenia-like conditions in a cell-based model system
M Kjalke, M Ezban, D M Monroe, et al.
Page
of 19
Search research articles
Search
Showing results (111-120 of 182) with videos related to
Sort By:
Page
of 19
British Journal of Haematology
|
February 1, 1980
An agarose plate method for detecting alloantisera to coagulant factor IX and factor IX antigen
H M Reisner, E A Strand, K S Chung, et al.
British Journal of Haematology
|
June 1, 1970
Continuous intravenous infusion of factor VIII in classic haemophilia
C W McMillan, W P Webster, H R Roberts, et al.
Archives of Internal Medicine
|
September 1, 1976
Hemolysis caused by factor VIII concentrates
E P Orringer, M J Koury, P M Blatt, et al.
Blood
|
October 1, 1980
Detection of factor IX antibodies by radioimmunoassay: effect of calcium on antibody-factor IX interaction
R M Lewis, H M Reisner, K S Chung, et al.
Blood
|
September 1, 1985
Comparison of inhibitory and binding characteristics of an antibody causing acquired von Willebrand syndrome: an assay for von Willebrand factor binding by antibody
W A Fricke, K M Brinkhous, J B Garris, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
September 14, 2001
Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic procedures
H A Cooper, C P Jones, E Campion, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 17, 2005
Cellular immune responses in hemophilia: why do inhibitors develop in some, but not all hemophiliacs?
G C White, C L Kempton, A Grimsley, et al.
Thrombosis and Haemostasis
|
October 31, 1979
Detection of an abnormal plasma clot structure by a simple rigidity assay
M E Carr, P M Blatt, H R Roberts, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 5, 1999
Newer concepts of blood coagulation
H R Roberts, D M Monroe, J A Oliver, et al.
British Journal of Haematology
|
July 27, 2001
High-dose factor VIIa increases initial thrombin generation and mediates faster platelet activation in thrombocytopenia-like conditions in a cell-based model system
M Kjalke, M Ezban, D M Monroe, et al.
Page
of 19