Ariella Zivelin

2016

Thromboembolic events in patients with severe inherited fibrinogen deficiency

Rottenstreich, A., Lask, A., Schliamser, L., Zivelin, A., Seligsohn, U. & Kalish, Y., 1 Aug 2016, In: Journal of Thrombosis and Thrombolysis. 42, 2, p. 261-266 6 p.

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

2015

The impact of thrombin generation and rotation thromboelastometry on assessment of severity of factor XI deficiency

Livnat, T., Shenkman, B., Martinowitz, U., Zivelin, A., Dardik, R., Tamarin, I., Mansharov, R., Budnik, I. & Salomon, O., 1 Aug 2015, In: Thrombosis Research. 136, 2, p. 465-473 9 p.

Research output: Contribution to journal › Article › peer-review

32 Scopus citations

2013

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., Sep 2013, In: Haemophilia. 19, 5, p. 782-789 8 p.

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews

Peretz, H., Salomon, O., Mor-cohen, R., Usher, S., Zucker, M., Zivelin, A. & Seligsohn, U., Apr 2013, In: Journal of Thrombosis and Haemostasis. 11, 4, p. 724-730 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

8 Scopus citations

2011

A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor

Livnat, T., Martinowitz, U., Zivelin, A., Rima, D. & Kenet, G., Apr 2011, In: Thrombosis and Haemostasis. 105, 4, p. 688-695 8 p.

Research output: Contribution to journal › Article › peer-review

25 Scopus citations

Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis

Salomon, O., Steinberg, D. M., Zucker, M., Varon, D., Zivelin, A. & Seligsohn, U., Feb 2011, In: Thrombosis and Haemostasis. 105, 2, p. 269-273 5 p.

Research output: Contribution to journal › Article › peer-review

192 Scopus citations

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., Oct 2011, In: Journal of Thrombosis and Haemostasis. 9, 10, p. 1977-1984 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

16 Scopus citations

Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry

Livnat, T., Shenkman, B., Kenet, G., Tamarin, I., Gillis, S., Varon, D., Iijima, K., Zivelin, A. & Salomon, O., Dec 2011, In: Blood Coagulation and Fibrinolysis. 22, 8, p. 673-679 7 p.

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

2010

[Laboratory evaluation of lupus anticoagulant in Israel].

Sarig, G., Garach-Jehoshua, O., Deutch, V., Winder, A., Hyam, E., Katz, B. Z., Lahav, J., Cassel, A., Zivelin, A., Souroujon, M., Shimron, O. & Israeli Sub-Committee of Thrombosis, S.-C. O. T., May 2010, In: Harefuah. 149, 5, p. 288-290, 336

Research output: Contribution to journal › Article › peer-review

Risk factors for failure of heparin thromboprophylaxis in patients with acute traumatic spinal cord injury

Rubin-Asher, D., Zeilig, G., Ratner, A., Asher, I., Zivelin, A., Seligsohn, U. & Lubetsky, A., Jun 2010, In: Thrombosis Research. 125, 6, p. 501-504 4 p.

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

2009

Concomitant infusion of low doses of rFVIIa and FEIBA in haemophilia patients with inhibitors

Martinowitz, U., Livnat, T., Zivelin, A. & Kenet, G., 2009, In: Haemophilia. 15, 4, p. 904-910 7 p.

Research output: Contribution to journal › Article › peer-review

52 Scopus citations

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., 2009, In: Haemophilia. 15, 3, p. 774-778 5 p.

Research output: Contribution to journal › Article › peer-review

20 Scopus citations

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., 2009, In: Journal of Thrombosis and Haemostasis. 7, 6, p. 970-975 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

15 Scopus citations

Thrombin generation assay as a possible tool for assessment of reduced activity of clotting factors induced by antiphospholipid antibodies and in-vitro evaluation of treatment options

Livnat, T., Zivelin, A., Tamarin, I., Guetta, V. & Salomon, O., Dec 2009, In: Blood Coagulation and Fibrinolysis. 20, 8, p. 661-666 6 p.

Research output: Contribution to journal › Article › peer-review

2008

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., Jul 2008, In: Haemophilia. 14, 4, p. 782-786 5 p.

Research output: Contribution to journal › Article › peer-review

43 Scopus citations

Induction of an inhibitor antibody to factor XI in a patient with severe inherited factor XI deficiency by Rh immune globulin

Zucker, M., Zivelin, A., Teitel, J. & Seligsohn, U., 2008, In: Blood. 111, 3, p. 1306-1308 3 p.

Research output: Contribution to journal › Article › peer-review

Open Access

13 Scopus citations

2007

Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations

Mor-Cohen, R., Zivelin, A., Fromovich-Amit, Y., Kovalski, V., Rosenberg, N. & Seligsohn, U., Mar 2007, In: Blood Coagulation and Fibrinolysis. 18, 2, p. 139-144 6 p.

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Characterization of seven novel mutations causing factor XI deficiency

Zucker, M., Zivelin, A., Landau, M., Salomon, O., Kenet, G., Bauduer, F., Samama, M., Conard, J., Denninger, M. H., Hani, A. S., Berruyer, M., Feinstein, D. & Seligsohn, U., Oct 2007, In: Haematologica. 92, 10, p. 1375-1380 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

28 Scopus citations

2006

Inhibitors to factor XI in patients with severe factor XI deficiency

Salomon, O., Zivelin, A., Livnat, T. & Seligsohn, U., Jan 2006, In: Seminars in Hematology. 43, SUPPL. 1, p. S10-S12

Research output: Contribution to journal › Article › peer-review

22 Scopus citations

Prerequisites for recombinant factor VIIa-induced thrombin generation in plasmas deficient in factors VIII, IX or XI

Livnat, T., Zivelin, A., Martinowitz, U., Salomon, O. & Seligsohn, U., Jan 2006, In: Journal of Thrombosis and Haemostasis. 4, 1, p. 192-200 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

44 Scopus citations

Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24 000 years ago

Zivelin, A., Mor-Cohen, R., Kovalsky, V., Kornbrot, N., Conard, J., Peyvandi, F., Kyrle, P. A., Bertina, R., Peyvandi, F., Emmerich, J. & Seligsohn, U., 15 Jun 2006, In: Blood. 107, 12, p. 4666-4668 3 p.

Research output: Contribution to journal › Article › peer-review

Open Access

43 Scopus citations

2005

A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients

Mor-Cohen, R., Zivelin, A., Rosenberg, N., Goldberg, I. & Seligsohn, U., Feb 2005, In: Hepatology Research. 31, 2, p. 104-111 8 p.

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation

Fromovich-Amit, Y., Zivelin, A., Rosenberg, N., Landau, M., Rosa, J. P. & Seligsohn, U., Jul 2005, In: Blood Coagulation and Fibrinolysis. 16, 5, p. 369-374 6 p.

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency

Salomon, O., Steinberg, D. M., Tamarin, I., Zivelin, A. & Seligsohn, U., Jan 2005, In: Blood Coagulation and Fibrinolysis. 16, 1, p. 37-41 5 p.

Research output: Contribution to journal › Article › peer-review

85 Scopus citations

2004

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., Jun 2004, In: Journal of Thrombosis and Haemostasis. 2, 6, p. 918-924 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

65 Scopus citations

A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia

Segal, A., Zivelin, A., Rosenberg, N., Ginsburg, D., Shpilberg, O. & Seligsohn, U., Jan 2004, In: Blood Coagulation and Fibrinolysis. 15, 1, p. 99-102 4 p.

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Fromovich-Amit, Y., Zivelin, A., Rosenberg, N., Tamary, H., Landau, M. & Seligsohn, U., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1774-1781 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

40 Scopus citations

Do platelets synthesize factor XI?

Gailani, D., Zivelin, A., Sinha, D. & Walsh, P. N., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1709-1712 4 p.

Research output: Contribution to journal › Article › peer-review

Open Access

17 Scopus citations

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., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1790-1797 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

29 Scopus citations

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., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1782-1789 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

22 Scopus citations

2003

High prevalences of vitamin B ₁₂ and folic acid deficiency in elderly subjects in Israel

Figlin, E., Chetrit, A., Shahar, A., Shpilberg, O., Zivelin, A., Rosenberg, N., Brok-Simoni, F., Gadoth, N., Sela, B. A. & Seligsohn, U., Nov 2003, In: British Journal of Haematology. 123, 4, p. 696-701 6 p.

Research output: Contribution to journal › Article › peer-review

38 Scopus citations

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., Apr 2003, In: Journal of Thrombosis and Haemostasis. 1, 4, p. 658-661 4 p.

Research output: Contribution to journal › Article › peer-review

Open Access

113 Scopus citations

Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus

Rosenberg, N., Yatuv, R., Sobolev, V., Peretz, H., Zivelin, A. & Seligsohn, U., 15 Jun 2003, In: Blood. 101, 12, p. 4808-4815 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

41 Scopus citations

Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiency

Salomon, O., Zivelin, A., Livnat, T., Dardik, R., Loewenthal, R., Avishai, O., Steinberg, D. M., Rosove, M. H., O'Connell, N., Lee, C. A. & Seligsohn, U., 15 Jun 2003, In: Blood. 101, 12, p. 4783-4788 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

112 Scopus citations

2002

Effects of platelet membrane glycoprotein polymorphisms on the risk of myocardial infarction in young males

Rosenberg, N., Zivelin, A., Chetrit, A., Dardik, R., Kornbrot, N., Freimark, D. & Inbal, A., 2002, In: Israel Medical Association Journal. 4, 6, p. 411-414 4 p.

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Zivelin, A., Bauduer, F., Ducout, L., Peretz, H., Rosenberg, N., Yatuv, R. & Seligsohn, U., 1 Apr 2002, In: Blood. 99, 7, p. 2448-2454 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

104 Scopus citations

The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans

Rosenberg, N., Murata, M., Ikeda, Y., Opare-Sem, O., Zivelin, A., Geffen, E. & Seligsohn, U., Mar 2002, In: American Journal of Human Genetics. 70, 3, p. 758-762 5 p.

Research output: Contribution to journal › Article › peer-review

Open Access

198 Scopus citations

2001

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., Chetrit, A., Eskaraev, R., Sela, B. A., Dardik, R., Zivelin, A., Ravid, B., Davidson, J., Seligsohn, U. & Inbal, A., 2001, In: Stroke. 32, 12, p. 2753-2758 6 p.

Research output: Contribution to journal › Article › peer-review

66 Scopus citations

Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

Mor-Cohen, R., Zivelin, A., Rosenberg, N., Shani, M., Muallem, S. & Seligsohn, U., 5 Oct 2001, In: Journal of Biological Chemistry. 276, 40, p. 36923-36930 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

113 Scopus citations

Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: Further lessons from Iraqi-Jewish Glanzmann thrombasthenia

Yatuv, R., Rosenberg, N., Zivelin, A., Peretz, H., Dardik, R., Trakhtenbrot, L. & Seligsohn, U., 15 Aug 2001, In: Blood. 98, 4, p. 1063-1069 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

21 Scopus citations

Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism

Salomon, O., Rosenberg, N., Zivelin, A., Steinberg, D. M., Kornbrot, N., Dardik, R., Inbal, A. & Seligsohn, U., 2001, In: Hematology Journal. 2, 1, p. 38-41 4 p.

Research output: Contribution to journal › Article › peer-review

22 Scopus citations

The role of factor XI in thrombin generation induced by low concentrations of tissue factor

Keularts, I. M. L. W., Zivelin, A., Seligsohn, U., Coenraad Hemker, H. & Béguin, S., 2001, In: Thrombosis and Haemostasis. 85, 6, p. 1060-1065 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

81 Scopus citations

2000

Homocysteine and oxidized low density lipoprotein enhance platelet adhesion to endothelial cells under flow conditions: Distinct mechanisms of thrombogenic modulation

Dardik, R., Varon, D., Tamarin, I., Zivelin, A., Salomon, O., Shenkman, B. & Savion, N., 2000, In: Thrombosis and Haemostasis. 83, 2, p. 338-344 7 p.

Research output: Contribution to journal › Article › peer-review

107 Scopus citations

Molecular characterization of four novel mutations causing factor VII deficiency

Tamary, H., Fromovich-Amit, Y., Shalmon, L., Zaizov, R., Yaniv, I., Klar, A., Peretz, H., Brenner, B., Lanir, N., Zivelin, A. & Seligsohn, U., 2000, In: Hematology Journal. 1, 6, p. 382-389 8 p.

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

1999

Analysis of prothrombotic and vascular risk factors in patients with nonarteritic anterior ischemic optic neuropathy

Salomon, O., Huna-Baron, R., Kurtz, S., Steinberg, D. M., Moisseiev, J., Rosenberg, N., Yassur, I., Vidne, O., Zivelin, A., Gitel, S., Davidson, J., Ravid, B. & Seligsohn, U., 1 Apr 1999, In: Ophthalmology. 106, 4, p. 739-742 4 p.

Research output: Contribution to journal › Article › peer-review

155 Scopus citations

ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families

Nichols, W. C., Terry, V. H., Wheatley, M. A., Yang, A., Zivelin, A., Ciavarella, N., Stefanile, C., Matsushita, T., Saito, H., De Bosch, N. B., Ruiz-Saez, A., Torres, A., Thompson, A. R., Feinstein, D. I., White, G. C., Negrier, C., Vinciguerra, C., Aktan, M., Kaufman, R. J. & Ginsburg, D. & 1 others, Seligsohn, U., 1 Apr 1999, In: Blood. 93, 7, p. 2261-2266 6 p.

Research output: Contribution to journal › Article › peer-review

72 Scopus citations

Extensive venous and arterial thrombosis associated with an inhibitor to activated protein C

Zivelin, A., Gitel, S., Griffin, J. H., Xu, X., Fernandez, J. A., Martinowitz, U., Cohen, Y., Halkin, H., Seligsohn, U. & Inbal, A., 1 Aug 1999, In: Blood. 94, 3, p. 895-901 7 p.

Research output: Contribution to journal › Article › peer-review

38 Scopus citations

Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII

Nichols, W. M., Seligsohn, U., Zivelin, A., Terry, V. H., Hertel, C. E., Wheatley, M. A., Moussalli, M. J., Hauri, H. P., Ciavarella, N., Kaufman, R. J., Ginsburg, D. & Sharon, N., Sep 1999, In: Chemtracts. 12, 10, p. 714-717 4 p.

Research output: Contribution to journal › Article › peer-review

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: Prevalence and risk assessment

Salomon, O., Steinberg, D. M., Zivelin, A., Gitel, S., Dardik, R., Rosenberg, N., Berliner, S., Inbal, A., Many, A., Lubetsky, A., Varon, D., Martinowitz, U. & Seligsohn, U., Mar 1999, In: Arteriosclerosis, Thrombosis, and Vascular Biology. 19, 3, p. 511-518 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

246 Scopus citations

1998

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., 1998, In: Blood Coagulation and Fibrinolysis. 9, 7, p. 617-622 6 p.

Research output: Contribution to journal › Article › peer-review

59 Scopus citations

Ariella Zivelin

Research output

Search results