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A Zivelin

Showing results (21-30 of 75) with videos related to

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Transfusion|March 1, 1984
Factor VII in plasma of women taking oral contraceptives. Lack of cold activation under blood bank conditionsU Seligsohn, A Zivelin, E Zwang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The laboratory diagnosis of haemophilia: Recommendations by the Laboratory Activities Committee of the World Federation of HemophiliaI Peake, U Seligsohn, S Gitel, et al.
Thrombosis and Haemostasis|March 11, 1998
Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytesN Rosenberg, R Dardik, E Rosenthal, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French BasquesF Bauduer, A Zivelin, L Ducout, et al.
British Journal of Haematology|March 1, 1984
Hereditary factor XIII deficiency: report of four families and definition of the carrier stateS Berliner, A Lusky, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Prerequisites for recombinant factor VIIa-induced thrombin generation in plasmas deficient in factors VIII, IX or XIT Livnat, A Zivelin, U Martinowitz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1992
The inheritance of type I and type III von Willebrand's disease in Israel: linkage analysis, carrier detection and prenatal diagnosis using three intragenic restriction fragment length polymorphismsA Inbal, N Kornbrot, A Zivelin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 13, 2009
Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutationD Landau, N Rosenberg, A Zivelin, et al.
British Journal of Haematology|March 1, 1986
A relatively high frequency of severe (type III) von Willebrand's disease in IsraelS A Berliner, U Seligsohn, A Zivelin, et al.
Blood|July 1, 1985
Inhibition of tissue factor/factor VIIa activity in plasma requires factor X and an additional plasma componentN L Sanders, S P Bajaj, A Zivelin, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Transfusion|March 1, 1984
Factor VII in plasma of women taking oral contraceptives. Lack of cold activation under blood bank conditionsU Seligsohn, A Zivelin, E Zwang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The laboratory diagnosis of haemophilia: Recommendations by the Laboratory Activities Committee of the World Federation of HemophiliaI Peake, U Seligsohn, S Gitel, et al.
Thrombosis and Haemostasis|March 11, 1998
Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytesN Rosenberg, R Dardik, E Rosenthal, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French BasquesF Bauduer, A Zivelin, L Ducout, et al.
British Journal of Haematology|March 1, 1984
Hereditary factor XIII deficiency: report of four families and definition of the carrier stateS Berliner, A Lusky, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
Prerequisites for recombinant factor VIIa-induced thrombin generation in plasmas deficient in factors VIII, IX or XIT Livnat, A Zivelin, U Martinowitz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1992
The inheritance of type I and type III von Willebrand's disease in Israel: linkage analysis, carrier detection and prenatal diagnosis using three intragenic restriction fragment length polymorphismsA Inbal, N Kornbrot, A Zivelin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 13, 2009
Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutationD Landau, N Rosenberg, A Zivelin, et al.
British Journal of Haematology|March 1, 1986
A relatively high frequency of severe (type III) von Willebrand's disease in IsraelS A Berliner, U Seligsohn, A Zivelin, et al.
Blood|July 1, 1985
Inhibition of tissue factor/factor VIIa activity in plasma requires factor X and an additional plasma componentN L Sanders, S P Bajaj, A Zivelin, et al.
Pageof 8