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A Zivelin

Showing results (41-50 of 75) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 2, 2011
Point mutations regarded as missense mutations cause splicing defects in the factor XI geneM Zucker, N Rosenberg, H Peretz, et al.
Blood|May 15, 1997
Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founderN Rosenberg, R Yatuv, Y Orion, et al.
American Journal of Clinical Pathology|January 1, 1992
Clinical significance of antibodies to bovine and human thrombin and factor V after surgical use of bovine thrombinS I Rapaport, A Zivelin, R A Minow, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patientsY Fromovich-Amit, A Zivelin, N Rosenberg, et al.
The Journal of Biological Chemistry|July 31, 2001
Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndromeR Mor-Cohen, A Zivelin, N Rosenberg, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The feasibility of using concentrates containing factor IX for continuous infusionS Schulman, S Gitel, A Zivelin, et al.
Thrombosis and Haemostasis|March 30, 2000
Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulationR Dardik, D Varon, I Tamarin, et al.
The New England Journal of Medicine|March 1, 1984
Homozygous protein C deficiency manifested by massive venous thrombosis in the newbornU Seligsohn, A Berger, M Abend, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2013
Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors--a thrombin generation-guided pilot studyT Livnat, U Martinowitz, S Azar-Avivi, et al.
American Journal of Hematology|December 1, 1995
Heparin-induced thrombocytopenia and fatal thrombosis in a patient with activated protein C resistanceJ Gardyn, P Sorkin, Y Kluger, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Journal of Thrombosis and Haemostasis : JTH|July 2, 2011
Point mutations regarded as missense mutations cause splicing defects in the factor XI geneM Zucker, N Rosenberg, H Peretz, et al.
Blood|May 15, 1997
Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founderN Rosenberg, R Yatuv, Y Orion, et al.
American Journal of Clinical Pathology|January 1, 1992
Clinical significance of antibodies to bovine and human thrombin and factor V after surgical use of bovine thrombinS I Rapaport, A Zivelin, R A Minow, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patientsY Fromovich-Amit, A Zivelin, N Rosenberg, et al.
The Journal of Biological Chemistry|July 31, 2001
Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndromeR Mor-Cohen, A Zivelin, N Rosenberg, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
The feasibility of using concentrates containing factor IX for continuous infusionS Schulman, S Gitel, A Zivelin, et al.
Thrombosis and Haemostasis|March 30, 2000
Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulationR Dardik, D Varon, I Tamarin, et al.
The New England Journal of Medicine|March 1, 1984
Homozygous protein C deficiency manifested by massive venous thrombosis in the newbornU Seligsohn, A Berger, M Abend, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2013
Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors--a thrombin generation-guided pilot studyT Livnat, U Martinowitz, S Azar-Avivi, et al.
American Journal of Hematology|December 1, 1995
Heparin-induced thrombocytopenia and fatal thrombosis in a patient with activated protein C resistanceJ Gardyn, P Sorkin, Y Kluger, et al.
Pageof 8