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Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 24, 2016
The feasibility of using concentrates containing factor IX for continuous infusion
S Schulman, S Gitel, A Zivelin, et al.
Thrombosis and Haemostasis
|
March 4, 1999
Safety and efficacy of continuous infusion of a combined factor VIII-von Willebrand factor (vWF) concentrate (Haemate-P) in patients with von Willebrand disease
A Lubetsky, S Schulman, D Varon, et al.
Journal of Medical Virology
|
June 1, 1993
Response of hemophilic patients to poliovirus vaccination: correlation with HIV serology and with immunological parameters
D Varon, R Handsher, R Dardik, et al.
Thrombosis and Haemostasis
|
September 1, 1993
Platelet aggregation on extracellular matrix: effect of a recombinant GPIb-binding fragment of von Willebrand factor
R Dardik, Z M Ruggeri, N Savion, et al.
Stroke
|
June 3, 2000
Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children
G Kenet, S Sadetzki, H Murad, et al.
The American Journal of Cardiology
|
December 1, 1998
Increased cardiovascular disease mortality rates in traumatic lower limb amputees
M Modan, E Peles, H Halkin, et al.
Thrombosis and Haemostasis
|
March 1, 1996
Feasibility of using recombinant factor VIIa in continuous infusion
S Schulman, M Bech Jensen, D Varon, et al.
British Journal of Haematology
|
January 1, 1997
Acquired von Willebrand disease in a patient with angiodysplasia resulting from immune-mediated clearance of von Willebrand factor
A Inbal, I Bank, A Zivelin, et al.
Pediatric Hematology and Oncology
|
October 1, 1993
Spectrum of clinical manifestations of antiphospholipid antibodies in childhood and adolescence
A Toren, P Toren, A Many, et al.
Blood
|
July 27, 1999
Extensive venous and arterial thrombosis associated with an inhibitor to activated protein C
A Zivelin, S Gitel, J H Griffin, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 24, 2016
The feasibility of using concentrates containing factor IX for continuous infusion
S Schulman, S Gitel, A Zivelin, et al.
Thrombosis and Haemostasis
|
March 4, 1999
Safety and efficacy of continuous infusion of a combined factor VIII-von Willebrand factor (vWF) concentrate (Haemate-P) in patients with von Willebrand disease
A Lubetsky, S Schulman, D Varon, et al.
Journal of Medical Virology
|
June 1, 1993
Response of hemophilic patients to poliovirus vaccination: correlation with HIV serology and with immunological parameters
D Varon, R Handsher, R Dardik, et al.
Thrombosis and Haemostasis
|
September 1, 1993
Platelet aggregation on extracellular matrix: effect of a recombinant GPIb-binding fragment of von Willebrand factor
R Dardik, Z M Ruggeri, N Savion, et al.
Stroke
|
June 3, 2000
Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children
G Kenet, S Sadetzki, H Murad, et al.
The American Journal of Cardiology
|
December 1, 1998
Increased cardiovascular disease mortality rates in traumatic lower limb amputees
M Modan, E Peles, H Halkin, et al.
Thrombosis and Haemostasis
|
March 1, 1996
Feasibility of using recombinant factor VIIa in continuous infusion
S Schulman, M Bech Jensen, D Varon, et al.
British Journal of Haematology
|
January 1, 1997
Acquired von Willebrand disease in a patient with angiodysplasia resulting from immune-mediated clearance of von Willebrand factor
A Inbal, I Bank, A Zivelin, et al.
Pediatric Hematology and Oncology
|
October 1, 1993
Spectrum of clinical manifestations of antiphospholipid antibodies in childhood and adolescence
A Toren, P Toren, A Many, et al.
Blood
|
July 27, 1999
Extensive venous and arterial thrombosis associated with an inhibitor to activated protein C
A Zivelin, S Gitel, J H Griffin, et al.
Page
of 3