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A Zivelin

Showing results (61-70 of 75) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Inherited factor XI deficiency confers no protection against acute myocardial infarctionO Salomon, D M Steinberg, R Dardik, 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 factorA Inbal, I Bank, A Zivelin, et al.
The Journal of Clinical Investigation|February 15, 1997
Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mappingW C Nichols, U Seligsohn, A Zivelin, et al.
The American Journal of Cardiology|July 15, 1989
Intermittent, dose-related fluctuations of pain and ST elevation during infusion of recombinant tissue plasminogen activator during acute myocardial infarctionG I Barbash, H Hod, S Rath, et al.
Blood|July 27, 1999
Extensive venous and arterial thrombosis associated with an inhibitor to activated protein CA Zivelin, S Gitel, J H Griffin, et al.
Thrombosis and Haemostasis|June 1, 1997
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiencyA Inbal, G Kenet, A Zivelin, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
The American Journal of Cardiology|December 1, 1989
Correlation of baseline plasminogen activator inhibitor activity with patency of the infarct artery after thrombolytic therapy in acute myocardial infarctionG I Barbash, H Hod, A Roth, et al.
Stroke|December 12, 2001
Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphismJ Y Streifler, N Rosenberg, A Chetrit, et al.
Blood|November 5, 1997
The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European originH Peretz, A Mulai, S Usher, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Inherited factor XI deficiency confers no protection against acute myocardial infarctionO Salomon, D M Steinberg, R Dardik, 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 factorA Inbal, I Bank, A Zivelin, et al.
The Journal of Clinical Investigation|February 15, 1997
Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mappingW C Nichols, U Seligsohn, A Zivelin, et al.
The American Journal of Cardiology|July 15, 1989
Intermittent, dose-related fluctuations of pain and ST elevation during infusion of recombinant tissue plasminogen activator during acute myocardial infarctionG I Barbash, H Hod, S Rath, et al.
Blood|July 27, 1999
Extensive venous and arterial thrombosis associated with an inhibitor to activated protein CA Zivelin, S Gitel, J H Griffin, et al.
Thrombosis and Haemostasis|June 1, 1997
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiencyA Inbal, G Kenet, A Zivelin, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular characterization of four novel mutations causing factor VII deficiencyH Tamary, Y Fromovich-Amit, L Shalmon, et al.
The American Journal of Cardiology|December 1, 1989
Correlation of baseline plasminogen activator inhibitor activity with patency of the infarct artery after thrombolytic therapy in acute myocardial infarctionG I Barbash, H Hod, A Roth, et al.
Stroke|December 12, 2001
Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphismJ Y Streifler, N Rosenberg, A Chetrit, et al.
Blood|November 5, 1997
The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European originH Peretz, A Mulai, S Usher, et al.
Pageof 8