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Ariella Zivelin

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Israel

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Hava Peretz; Ophira Salomon; Saly Usher; Ariella Zivelin; Michal Zucker; Ronit Mor-Cohen; Uri Seligsohn
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.
Michal Zucker; Ariella Zivelin; Frédéric Bauduer; D Green; H Peretz; Nurit Rosenberg; Uri Seligsohn
Point mutations regarded as missense mutations cause splicing defects in the factor XI gene.
Tamar Livnat; Uri martinowitz; Ariella Zivelin; Dardik Rima; Gili Kenet
A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor.

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2013: Hava Peretz; Ophira Salomon; Saly Usher; Ariella Zivelin; Michal Zucker; Ronit Mor-Cohen; Uri Seligsohn
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.
Journal of thrombosis and haemostasis : JTH 2013;11(4):724-30.
2011: Michal Zucker; Ariella Zivelin; Frédéric Bauduer; D Green; H Peretz; Nurit Rosenberg; Uri Seligsohn
Point mutations regarded as missense mutations cause splicing defects in the factor XI gene.
Journal of thrombosis and haemostasis : JTH 2011;9(10):1977-84.
2011: Tamar Livnat; Uri martinowitz; Ariella Zivelin; Dardik Rima; Gili Kenet
A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor.
Thrombosis and haemostasis 2011;105(4):688-95.
2011: Ophira Salomon; David M Steinberg; Michal Zucker; David Varon; Ariella Zivelin; Uri Seligsohn
Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis.
Thrombosis and haemostasis 2011;105(2):269-73.
2010: Deborah Rubin-Asher; Gabriel Zeilig; Aba Ratner; Ilan Asher; Ariella Zivelin; Uri Seligsohn; Aaron Lubetsky
Risk factors for failure of heparin thromboprophylaxis in patients with acute traumatic spinal cord injury.
Thrombosis research 2010;125(6):501-4.
2010: Galit Sarig; Osnat Garach-Jehoshua; Varda Deutch; Asher Winder; Esti Hyam; Ben Zion Katz; Judith Lahav; Aliza Cassel; Ariella Zivelin; Moshe Souroujon; Orit Shimron
[Laboratory evaluation of lupus anticoagulant in Israel].
Harefuah 2010;149(5):288-90, 336.
2009: Tami Livnat; Ariella Zivelin; Ilia Tamarin; Victor Guetta; Ophira Salomon
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.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009;20(8):661-6.
2009: Michal Zucker; Ariella Zivelin; meytal landau; Nurit Rosenberg; Uri Seligsohn
Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI.
Journal of thrombosis and haemostasis : JTH 2009;7(6):970-5.
2008: Tamar Livnat; Uri Martinowitz; Ariella Zivelin; Uri Seligsohn
Effects of factor VIII inhibitor bypassing activity (FEIBA), recombinant factor VIIa or both on thrombin generation in normal and haemophilia A plasma.
Haemophilia : the official journal of the World Federation of Hemophilia 2008;14(4):782-6.
2008: Michal Zucker; Ariella Zivelin; Jerome Teitel; Uri Seligsohn
Induction of an inhibitor antibody to factor XI in a patient with severe inherited factor XI deficiency by Rh immune globulin.
Blood 2008;111(3):1306-8.
2007: Michal Zucker; Ariella Zivelin; meytal landau; Ophira Salomon; Gili Kenet; Frédéric Bauduer; Michel Samama; Jacqueline Conard; Marie-Hélène Denninger; Abu-Samra Hani; Micheline Berruyer; Donald Feinstein; Uri Seligsohn
Characterization of seven novel mutations causing factor XI deficiency.
Haematologica 2007;92(10):1375-80.
2007: Ronit Mor-Cohen; Ariella Zivelin; Yonit Fromovich-Amit; Victoria Kovalski; Nurit Rosenberg; Uri Seligsohn
Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2007;18(2):139-44.
2006: Ariella Zivelin; Ronit Mor-Cohen; Victoria Kovalsky; Nurit Kornbrot; Jacqueline Conard; Flora Peyvandi; Paul A Kyrle; Rogier Bertina; Flora Peyvandi; Joseph Emmerich; Uri Seligsohn
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years ago.
Blood 2006;107(12):4666-8.
2006: Ophira Salomon; Ariella Zivelin; Tami Livnat; Uri Seligsohn
Inhibitors to Factor XI in patients with severe Factor XI deficiency.
Seminars in hematology 2006;43(1 Suppl 1):S10-2.
2006: Tami Livnat; Ariella Zivelin; Uri Martinowitz; Ophira Salomon; Uri Seligsohn
Prerequisites for recombinant factor VIIa-induced thrombin generation in plasmas deficient in factors VIII, IX or XI.
Journal of thrombosis and haemostasis : JTH 2006;4(1):192-200.
2005: Yonit Fromovich-Amit; Ariella Zivelin; Nurit Rosenberg; meytal landau; Jean-Philippe Rosa; Uri Seligsohn
Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2005;16(5):369-74.
2005: Ronit Mor-Cohen; Ariella Zivelin; Nurit Rosenberg; Iris Goldberg; Uri Seligsohn
A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients.
Hepatology research : the official journal of the Japan Society of Hepatology 2005;31(2):104-11.
2005: Ophira Salomon; David M Steinberg; Ilia Tamarin; Ariella Zivelin; Uri Seligsohn
Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2005;16(1):37-41.
2004: A Vysokovsky; R Saxena; meytal landau; Ariella Zivelin; Regina Eskaraev; Nurit Rosenberg; Uri Seligsohn; Aida Inbal
Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families.
Journal of thrombosis and haemostasis : JTH 2004;2(10):1790-7.
2004: Ariella Zivelin; T Ogawa; S Bulvik; meytal landau; John R Toomey; jacqueline lane; Uri Seligsohn; David Gailani
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.
Journal of thrombosis and haemostasis : JTH 2004;2(10):1782-9.
2004: Yonit Fromovich-Amit; Ariella Zivelin; Nurit Rosenberg; Hannah Tamary; meytal landau; Uri Seligsohn
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients.
Journal of thrombosis and haemostasis : JTH 2004;2(10):1774-81.
2004: David Gailani; Ariella Zivelin; D Sinha; Peter N Walsh
Do platelets synthesize factor XI?
Journal of thrombosis and haemostasis : JTH 2004;2(10):1709-12.
2004: Paula H B Bolton-Maggs; Hava Peretz; R Butler; R Mountford; S Keeney; L Zacharski; Ariella Zivelin; U Seligsohn
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency.
Journal of thrombosis and haemostasis : JTH 2004;2(6):918-24.
2004: Frédéric Bauduer; Ariella Zivelin; Louis Ducout; E Shpringer; Uri Seligsohn
The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques.
Journal of thrombosis and haemostasis : JTH 2004;2(2):361-2.
2004: Avichai Segal; Ariella Zivelin; Nurit Rosenberg; David Ginsburg; Ofer Shpilberg; Uri Seligsohn
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.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(1):99-102.
2003: Elizabeth Figlin; Angela Chetrit; Avner Shahar; Ofer Shpilberg; Ariella Zivelin; Nurit Rosenberg; Frida Brok-Simoni; Natan Gadoth; Ben-Ami Sela; Uri Seligsohn
High prevalences of vitamin B12 and folic acid deficiency in elderly subjects in Israel.
British journal of haematology 2003;123(4):696-701.
2003: Nurit Rosenberg; Rivka Yatuv; Vladimir Sobolev; Hava Peretz; Ariella Zivelin; Uri Seligsohn
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.
Blood 2003;101(12):4808-15.
2003: Ophira Salomon; Ariella Zivelin; Tami Livnat; Rima Dardik; Ron Loewenthal; Ophelia Avishai; David M Steinberg; Michael H Rosove; Niamh O'Connell; Christine A Lee; Uri Seligsohn
Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiency.
Blood 2003;101(12):4783-8.
2003: Ophira Salomon; David M Steinberg; Rima Dardik; Nurit Rosenberg; Ariella Zivelin; Ilia Tamarin; Bruria Ravid; S Berliner; Uri Seligsohn
Inherited factor XI deficiency confers no protection against acute myocardial infarction.
Journal of thrombosis and haemostasis : JTH 2003;1(4):658-61.
2002: Nurit Rosenberg; Ariella Zivelin; Angela Chetrit; Rima Dardik; Nurit Kornbrot; Dov Freimark; Aida Inbal
Effects of platelet membrane glycoprotein polymorphisms on the risk of myocardial infarction in young males.
The Israel Medical Association journal : IMAJ 2002;4(6):411-4.
2002: Ariella Zivelin; Frédéric Bauduer; Louis Ducout; Hava Peretz; Nurit Rosenberg; Rivka Yatuv; Uri Seligsohn
Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene.
Blood 2002;99(7):2448-54.
2002: Nurit Rosenberg; Mitsuru Murata; Yasuo Ikeda; Ohene Opare-Sem; Ariella Zivelin; Eli Geffen; Uri Seligsohn
The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans.
American journal of human genetics 2002;70(3):758-62.
2001: Jonathan Y Streifler; Nurit Rosenberg; A Chetrit; Regina Eskaraev; B A Sela; Rima Dardik; Ariella Zivelin; Bruria Ravid; Jacquelin Davidson; Uri Seligsohn; Aida Inbal
Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphism.
Stroke; a journal of cerebral circulation 2001;32(12):2753-8.
2001: Ronit Mor-Cohen; Ariella Zivelin; Nurit Rosenberg; M Shani; S Muallem; Uri Seligsohn
Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndrome.
The Journal of biological chemistry 2001;276(40):36923-30.
2001: Rivka Yatuv; Nurit Rosenberg; Ariella Zivelin; Hava Peretz; Rima Dardik; Luba Trakhtenbrot; Uri Seligsohn
Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia.
Blood 2001;98(4):1063-9.
2001: Ophira Salomon; Nurit Rosenberg; Ariella Zivelin; David M Steinberg; Nurit Kornbrot; Rima Dardik; Aida Inbal; Uri Seligsohn
Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism.
The hematology journal : the official journal of the European Haematology Association / EHA 2001;2(1):38-41.
2000: Rima Dardik; David Varon; Ilia Tamarin; Ariella Zivelin; Ophira Salomon; Boris Shenkman; Naphtali Savion
Homocysteine and oxidized low density lipoprotein enhanced platelet adhesion to endothelial cells under flow conditions: distinct mechanisms of thrombogenic modulation.
Thrombosis and haemostasis 2000;83(2):338-44.
2000: Hannah Tamary; Yonit Fromovich-Amit; Lea Shalmon; Rina Zaizov; Isaac Yaniv; A Klar; Hava Peretz; B Brenner; Naomi Lanir; Ariella Zivelin; Uri Seligsohn
Molecular characterization of four novel mutations causing factor VII deficiency.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(6):382-9.
1999: Ariella Zivelin; S Gitel; J H Griffin; X Xu; J A Fernandez; Uri Martinowitz; Y Cohen; H Halkin; Uri Seligsohn; Aida Inbal
Extensive venous and arterial thrombosis associated with an inhibitor to activated protein C.
Blood 1999;94(3):895-901.
1999: Ophira Salomon; Ruth Huna-Baron; Shimon Kurtz; David M Steinberg; Joseph Moisseiev; Nurit Rosenberg; I Yassur; O Vidne; Ariella Zivelin; S Gitel; Jacquelin Davidson; Bruria Ravid; Uri Seligsohn
Analysis of prothrombotic and vascular risk factors in patients with nonarteritic anterior ischemic optic neuropathy.
Ophthalmology 1999;106(4):739-42.
1999: Ophira Salomon; David M Steinberg; Ariella Zivelin; S Gitel; Rima Dardik; Nurit Rosenberg; S Berliner; Aida Inbal; A Many; Aharon Lubetsky; David Varon; Uri Martinowitz; Uri Seligsohn
Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.
Arteriosclerosis, thrombosis, and vascular biology 1999;19(3):511-8.
1998: Ophira Salomon; Joseph Moisseiev; Nurit Rosenberg; O Vidne; I Yassur; Ariella Zivelin; Giora Treister; David M Steinberg; Uri Seligsohn
Analysis of genetic polymorphisms related to thrombosis and other risk factors in patients with retinal vein occlusion.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1998;9(7):617-22.
1998: Ariella Zivelin; Nurit Rosenberg; S Faier; Nurit Kornbrot; Hava Peretz; C Mannhalter; M H Horellou; Uri Seligsohn
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene.
Blood 1998;92(4):1119-24.
1998: Nurit Rosenberg; Rima Dardik; Eti Rosenthal; Ariella Zivelin; Uri Seligsohn
Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytes.
Thrombosis and haemostasis 1998;79(2):244-8.
1997: Benjamin Brenner; A Laor; H Lupo; Ariella Zivelin; Naomi Lanir; Uri Seligsohn
Bleeding predictors in factor-XI-deficient patients.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1997;8(8):511-5.
1997: Hava Peretz; A Mulai; Saly Usher; Ariella Zivelin; A Segal; Z Weisman; M Mittelman; H Lupo; Naomi Lanir; B Brenner; Ofer Shpilberg; Uri Seligsohn
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.
Blood 1997;90(7):2654-9.
1997: Ariella Zivelin; N Rosenberg; Hava Peretz; Y Amit; Nurit Kornbrot; U Seligsohn
Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes.
Clinical chemistry 1997;43(9):1657-9.
1997: Uri Seligsohn; Ariella Zivelin
Thrombophilia as a multigenic disorder.
Thrombosis and haemostasis 1997;78(1):297-301.
1997: Aida Inbal; Gili Kenet; Ariella Zivelin; T Yermiyahu; T Bronstein; T Sheinfeld; H Tamari; S Gitel; G Eshel; J Duchemin; M Aiach; Uri Seligsohn
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiency.
Thrombosis and haemostasis 1997;77(6):1086-9.
1997: Aida Inbal; V C Yee; Nurit Kornbrot; Ariella Zivelin; B Brenner; Uri Seligsohn
Factor XIII deficiency due to a Leu660Pro mutation in the factor XIII subunit-a gene in three unrelated Palestinian Arab families.
Thrombosis and haemostasis 1997;77(6):1062-7.
1997: Nurit Rosenberg; Rivka Yatuv; Y Orion; Ariella Zivelin; Rima Dardik; Hava Peretz; Uri Seligsohn
Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founder.
Blood 1997;89(10):3654-62.
1997: Ariella Zivelin; J H Griffin; X Xu; I Pabinger; M Samama; Jacqueline Conard; B Brenner; Amiram Eldor; Uri Seligsohn
A single genetic origin for a common Caucasian risk factor for venous thrombosis.
Blood 1997;89(2):397-402.
1997: Aida Inbal; I Bank; Ariella Zivelin; David Varon; Rima Dardik; R Shapiro; Eti Rosenthal; Boris Shenkman; S Gitel; Uri Seligsohn
Acquired von Willebrand disease in a patient with angiodysplasia resulting from immune-mediated clearance of von Willebrand factor.
British journal of haematology 1997;96(1):179-82.
1996: Benjamin Brenner; Ariella Zivelin; Naomi Lanir; J S Greengard; J H Griffin; Uri Seligsohn
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 thrombosis.
Blood 1996;88(3):877-80.
1996: Hava Peretz; Ariella Zivelin; Saly Usher; Uri Seligsohn
A 14-bp deletion (codon 554 del AAGgtaacagagtg) at exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency.
Human mutation 1996;8(1):77-8.
1995: O Shpilberg; Hava Peretz; Ariella Zivelin; Rivka Yatuv; A Chetrit; Tamar Ringel-Kulka; C Stern; E Weiss; Uri Seligsohn
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 Jews.
Blood 1995;85(2):429-32.
1992: Aida Inbal; Nurit Kornbrot; Ariella Zivelin; M Shaklai; Uri Seligsohn
The inheritance of type I and type III von Willebrand's disease in Israel: linkage analysis, carrier detection and prenatal diagnosis using three intragenic restriction fragment length polymorphisms.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1992;3(2):167-77.
1990: Benjamin Brenner; S Tavori; Ariella Zivelin; C B Keller; J W Suttie; I Tatarsky; Uri Seligsohn
Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants.
British journal of haematology 1990;75(4):537-42.
1989: O Ben-Tal; Ariella Zivelin; Uri Seligsohn
The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel.
Thrombosis and haemostasis 1989;61(1):50-4.