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Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Inherited factor XI deficiency confers no protection against acute myocardial infarction
O 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 factor
A 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 mapping
W 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 infarction
G I Barbash, H Hod, S Rath, 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.
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 deficiency
A 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 deficiency
H 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 infarction
G 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) polymorphism
J 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 origin
H Peretz, A Mulai, S Usher, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Inherited factor XI deficiency confers no protection against acute myocardial infarction
O 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 factor
A 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 mapping
W 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 infarction
G I Barbash, H Hod, S Rath, 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.
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 deficiency
A 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 deficiency
H 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 infarction
G 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) polymorphism
J 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 origin
H Peretz, A Mulai, S Usher, et al.
Page
of 8