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A Zivelin

Showing results (31-40 of 75) with videos related to

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Thrombosis Research|October 1, 1987
Partial purification and characterization of extrinsic pathway inhibitor (the factor Xa-dependent plasma inhibitor of factor VIIa/tissue factor)B J Warn-Cramer, S L Maki, A Zivelin, et al.
Clinical Chemistry|September 23, 1997
Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymesA Zivelin, N Rosenberg, H Peretz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 10, 1998
Bleeding predictors in factor-XI-deficient patientsB Brenner, A Laor, H Lupo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Combined factors V and VIII deficiency--the solutionD Ginsburg, W C Nichols, A Zivelin, et al.
British Journal of Haematology|July 1, 1989
Immunoblot analysis of platelet glycoprotein IIb in patients with Glanzmann thrombasthenia in IsraelU Seligsohn, B S Coller, A Zivelin, et al.
Thrombosis and Haemostasis|June 1, 1997
Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab familiesA Inbal, V C Yee, N Kornbrot, et al.
British Journal of Haematology|April 1, 1986
Immunologic and biochemical characterization of homozygous and heterozygous Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations of Israel: comparison of techniques for carrier detectionB S Coller, U Seligsohn, A Zivelin, et al.
Thrombosis and Haemostasis|July 4, 2001
The role of factor XI in thrombin generation induced by low concentrations of tissue factorI M Keularts, A Zivelin, U Seligsohn, et al.
Blood|August 1, 1996
Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosisB Brenner, A Zivelin, N Lanir, et al.
Blood|August 9, 2001
Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombastheniaR Yatuv, N Rosenberg, A Zivelin, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Thrombosis Research|October 1, 1987
Partial purification and characterization of extrinsic pathway inhibitor (the factor Xa-dependent plasma inhibitor of factor VIIa/tissue factor)B J Warn-Cramer, S L Maki, A Zivelin, et al.
Clinical Chemistry|September 23, 1997
Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymesA Zivelin, N Rosenberg, H Peretz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 10, 1998
Bleeding predictors in factor-XI-deficient patientsB Brenner, A Laor, H Lupo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Combined factors V and VIII deficiency--the solutionD Ginsburg, W C Nichols, A Zivelin, et al.
British Journal of Haematology|July 1, 1989
Immunoblot analysis of platelet glycoprotein IIb in patients with Glanzmann thrombasthenia in IsraelU Seligsohn, B S Coller, A Zivelin, et al.
Thrombosis and Haemostasis|June 1, 1997
Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab familiesA Inbal, V C Yee, N Kornbrot, et al.
British Journal of Haematology|April 1, 1986
Immunologic and biochemical characterization of homozygous and heterozygous Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations of Israel: comparison of techniques for carrier detectionB S Coller, U Seligsohn, A Zivelin, et al.
Thrombosis and Haemostasis|July 4, 2001
The role of factor XI in thrombin generation induced by low concentrations of tissue factorI M Keularts, A Zivelin, U Seligsohn, et al.
Blood|August 1, 1996
Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosisB Brenner, A Zivelin, N Lanir, et al.
Blood|August 9, 2001
Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombastheniaR Yatuv, N Rosenberg, A Zivelin, et al.
Pageof 8