Geographic distribution of the 20210 G to A prothrombin variant
Rosendaal, F R, Doggen, C J, Zivelin, A, Arruda, V R, Aiach, M, Siscovick, D S, Hillarp, A, Watzke, H H, Bernardi, F, Cumming, A M, Preston, F E, Reitsma, P H
Published in Thrombosis and haemostasis (01.04.1998)
Published in Thrombosis and haemostasis (01.04.1998)
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Point mutations regarded as missense mutations cause splicing defects in the factor XI gene
ZUCKER, M., ROSENBERG, N., PERETZ, H., GREEN, D., BAUDUER, F., ZIVELIN, A., SELIGSOHN, U.
Published in Journal of thrombosis and haemostasis (01.10.2011)
Published in Journal of thrombosis and haemostasis (01.10.2011)
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Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors - a thrombin generation-guided pilot study
Livnat, T., Martinowitz, U., Azar-Avivi, S., Zivelin, A., Brutman-Barazani, T., Lubetsky, A., Kenet, G.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2013)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2013)
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Effects of factor VIII inhibitor bypassing activity (FEIBA), recombinant factor VIIa or both on thrombin generation in normal and haemophilia A plasma
LIVNAT, T., MARTINOWITZ, U., ZIVELIN, A., SELIGSOHN, U.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2008)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2008)
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Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI
ZUCKER, M., ZIVELIN, A., LANDAU, M., ROSENBERG, N., SELIGSOHN, U.
Published in Journal of thrombosis and haemostasis (01.06.2009)
Published in Journal of thrombosis and haemostasis (01.06.2009)
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Inherited factor XI deficiency confers no protection against acute myocardial infarction
Salomon, O., Steinberg, D. M., Dardik, R., Rosenberg, N., Zivelin, A., Tamarin, I., Ravid, B., Berliner, S., Seligsohn, U.
Published in Journal of thrombosis and haemostasis (01.04.2003)
Published in Journal of thrombosis and haemostasis (01.04.2003)
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Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation
LANDAU, D., ROSENBERG, N., ZIVELIN, A., STARETZ-CHACHAM, O., KAPELUSHNIK, J.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.05.2009)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.05.2009)
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A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency
Bolton‐Maggs, P. H. B., Peretz, H., Butler, R., Mountford, R., Keeney, S., Zacharski, L., Zivelin, A., Seligsohn, U.
Published in Journal of thrombosis and haemostasis (01.06.2004)
Published in Journal of thrombosis and haemostasis (01.06.2004)
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The role of factor XI in thrombin generation induced by low concentrations of tissue factor
Keularts, I M, Zivelin, A, Seligsohn, U, Hemker, H C, Béguin, S
Published in Thrombosis and haemostasis (01.06.2001)
Published in Thrombosis and haemostasis (01.06.2001)
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Seven novel mutations in the factor XIII A‐subunit gene causing hereditary factor XIII deficiency in 10 unrelated families
Vysokovsky, A., Saxena, R., Landau, M., Zivelin, A., Eskaraev, R., Rosenberg, N., Seligsohn, U., Inbal, A.
Published in Journal of thrombosis and haemostasis (01.10.2004)
Published in Journal of thrombosis and haemostasis (01.10.2004)
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Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphism
STREIFLER, J. Y, ROSENBERG, N, INBAL, A, CHETRIT, A, ESKARAEV, R, SELA, B. A, DARDIK, R, ZIVELIN, A, RAVID, B, DAVIDSON, J, SELIGSOHN, U
Published in Stroke (1970) (01.12.2001)
Published in Stroke (1970) (01.12.2001)
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Do platelets synthesize factor XI?
Gailani, D., Zivelin, A., Sinha, D., Walsh, P. N.
Published in Journal of thrombosis and haemostasis (01.10.2004)
Published in Journal of thrombosis and haemostasis (01.10.2004)
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Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI–Glu555): a cross‐reactive material positive variant defective in factor IX activation
Zivelin, A., Ogawa, T., Bulvik, S., Landau, M., Toomey, J. R., Lane, J., Seligsohn, U., Gailani, D.
Published in Journal of thrombosis and haemostasis (01.10.2004)
Published in Journal of thrombosis and haemostasis (01.10.2004)
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The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques
Bauduer, F., Zivelin, A., Ducout, L., Shpringer, E., Seligsohn, U.
Published in Journal of thrombosis and haemostasis (01.02.2004)
Published in Journal of thrombosis and haemostasis (01.02.2004)
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Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusion
Salomon, O, Moisseiev, J, Rosenberg, N, Vidne, O, Yassur, I, Zivelin, A, Treister, G, Steinberg, D M, Seligsohn, U
Published in Blood coagulation & fibrinolysis (01.10.1998)
Published in Blood coagulation & fibrinolysis (01.10.1998)
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