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A Zivelin

Showing results (51-60 of 75) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
British Journal of Haematology|August 1, 1990
Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulantsB Brenner, S Tavori, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated familiesA Vysokovsky, R Saxena, M Landau, et al.
Blood|January 15, 1995
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of JewsO Shpilberg, H Peretz, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): a cross-reactive material positive variant defective in factor IX activationA Zivelin, T Ogawa, S Bulvik, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolismO Salomon, N Rosenberg, A Zivelin, et al.
Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
Blood|January 15, 1997
A single genetic origin for a common Caucasian risk factor for venous thrombosisA Zivelin, J H Griffin, X Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusionO Salomon, J Moisseiev, N Rosenberg, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2004
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiencyP H B Bolton-Maggs, H Peretz, R Butler, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
British Journal of Haematology|August 1, 1990
Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulantsB Brenner, S Tavori, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated familiesA Vysokovsky, R Saxena, M Landau, et al.
Blood|January 15, 1995
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of JewsO Shpilberg, H Peretz, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2004
Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): a cross-reactive material positive variant defective in factor IX activationA Zivelin, T Ogawa, S Bulvik, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolismO Salomon, N Rosenberg, A Zivelin, et al.
Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
Blood|January 15, 1997
A single genetic origin for a common Caucasian risk factor for venous thrombosisA Zivelin, J H Griffin, X Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusionO Salomon, J Moisseiev, N Rosenberg, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2004
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiencyP H B Bolton-Maggs, H Peretz, R Butler, et al.
Pageof 8