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Journal Articles

Patients with Severe Factor XI Deficiency Have a Reduced Incidence of Venous Thromboembolism.

Ophira Salomon, Ariella Zivelin, Ilia Tamarin, David M. Steinberg, David Varon, MD, Uri Seligsohn, MD

Blood (2009) 114 (22): 3491.

https://doi.org/10.1182/blood.V114.22.3491.3491

Published: 2009

Journal Articles

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

Michal Zucker, Ariella Zivelin, Jerome Teitel, Uri Seligsohn

Blood (2008) 111 (3): 1306–1308.

https://doi.org/10.1182/blood-2007-08-108449

Published: 2008

Journal Articles

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

Ariella Zivelin, Ronit Mor-Cohen, Victoria Kovalsky, Nurit Kornbrot, Jacqueline Conard, Flora Peyvandi, Paul A. Kyrle, Rogier Bertina, Ferial Peyvandi, Joseph Emmerich, Uri Seligsohn

Blood (2006) 107 (12): 4666–4668.

https://doi.org/10.1182/blood-2005-12-5158

Published: 2006

Journal Articles

The Prothrombotic Polymorphism Prothrombin G20210A Is an Ancestral Mutation That Arose in Caucasians Approximately 20,000 Years Ago.

Ariella Zivelin, PhD, Ronit Mor-Cohen, PhD, Victoria Kovalsky, Jacqueline Conard, PhD, Flora Peyvandi, MD, Ingrid Pabinger, MD, Rogier Bertina, PhD, Ferial Peyvandi, MD, Joseph Emmerich, MD, Uri Seligsohn, MD

Blood (2005) 106 (11): 729.

https://doi.org/10.1182/blood.V106.11.729.729

Published: 2005

Journal Articles

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

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

Blood (2003) 101 (12): 4783–4788.

https://doi.org/10.1182/blood-2002-09-2794

Published: 2003

Journal Articles

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

Nurit Rosenberg, Rivka Yatuv, Vladimir Sobolev, Hava Peretz, Ariella Zivelin, Uri Seligsohn

Blood (2003) 101 (12): 4808–4815.

https://doi.org/10.1182/blood-2002-08-2452

Published: 2003

Journal Articles

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

Ariella Zivelin, Frederic Bauduer, Louis Ducout, Hava Peretz, Nurit Rosenberg, Rivka Yatuv, Uri Seligsohn

Blood (2002) 99 (7): 2448–2454.

https://doi.org/10.1182/blood.V99.7.2448

Published: 2002

Journal Articles

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

Rivka Yatuv, Nurit Rosenberg, Ariella Zivelin, Hava Peretz, Rima Dardik, Luba Trakhtenbrot, Uri Seligsohn

Blood (2001) 98 (4): 1063–1069.

https://doi.org/10.1182/blood.V98.4.1063

Published: 2001

Journal Articles

Extensive Venous and Arterial Thrombosis Associated With an Inhibitor to Activated Protein C

Ariella Zivelin, Sanford Gitel, John H. Griffin, Xiao Xu, Jose A. Fernandez, Uri Martinowitz, Yael Cohen, Hillel Halkin, Uri Seligsohn, Aida Inbal

Blood (1999) 94 (3): 895–901.

https://doi.org/10.1182/blood.V94.3.895.415k01_895_901

Published: 1999

Journal Articles

ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families

Blood (1999) 93 (7): 2261–2266.

https://doi.org/10.1182/blood.V93.7.2261

Published: 1999

Journal Articles

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Ariella Zivelin, Nurit Rosenberg, Shlomit Faier, Nurit Kornbrot, Hava Peretz, Christine Mannhalter, Marie Helene Horellou, Uri Seligsohn

Blood (1998) 92 (4): 1119–1124.

https://doi.org/10.1182/blood.V92.4.1119

Published: 1998

Journal Articles

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

Hava Peretz, Avital Mulai, Sali Usher, Ariella Zivelin, Avihai Segal, Zahavi Weisman, Moshe Mittelman, Hannah Lupo, Naomi Lanir, Benjamin Brenner, Ofer Shpilberg, Uri Seligsohn

Blood (1997) 90 (7): 2654–2659.

https://doi.org/10.1182/blood.V90.7.2654

Published: 1997

Journal Articles

Glanzmann Thrombasthenia Caused by an 11.2-kb Deletion in the Glycoprotein IIIa (β 3 ) Is a Second Mutation in Iraqi Jews That Stemmed From a Distinct Founder

Nurit Rosenberg, Rivka Yatuv, Yael Orion, Ariella Zivelin, Rima Dardik, Hava Peretz, Uri Seligsohn

Blood (1997) 89 (10): 3654–3662.

https://doi.org/10.1182/blood.V89.10.3654

Published: 1997

Journal Articles

A Single Genetic Origin for a Common Caucasian Risk Factor for Venous Thrombosis

Ariella Zivelin, John H. Griffin, Xiao Xu, Ingrid Pabinger, Michel Samama, Jacqueline Conard, Benjamin Brenner, Amiram Eldor, Uri Seligsohn

Blood (1997) 89 (2): 397–402.

https://doi.org/10.1182/blood.V89.2.397

Published: 1997

NARROW

Patients with Severe Factor XI Deficiency Have a Reduced Incidence of Venous Thromboembolism.

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

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

The Prothrombotic Polymorphism Prothrombin G20210A Is an Ancestral Mutation That Arose in Caucasians Approximately 20,000 Years Ago.

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

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

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

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

Extensive Venous and Arterial Thrombosis Associated With an Inhibitor to Activated Protein C

ERGIC-53 Gene Structure and Mutation Analysis in 19 Combined Factors V and VIII Deficiency Families

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

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

Glanzmann Thrombasthenia Caused by an 11.2-kb Deletion in the Glycoprotein IIIa (β 3 ) Is a Second Mutation in Iraqi Jews That Stemmed From a Distinct Founder

A Single Genetic Origin for a Common Caucasian Risk Factor for Venous Thrombosis

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American Society of Hematology

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American Society of Hematology

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