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Journal Articles

Endogenous Thrombin Potential (ETP) in Patients with Hereditary Antithrombin (AT) Deficiency or Carriers of the Prothrombin (PT) 20210A Gene Mutation.

Jacqueline Conard, PhD, Nicolas Soustelle, Laura Plouy, Marie-Helene Horellou, MD, Meyer-Michel Samama, MD

Blood (2007) 110 (11): 1623.

https://doi.org/10.1182/blood.V110.11.1623.1623

Published: 2007

Journal Articles

JAK2 V617F in 3 Patients with Venous Thromboembolism (VTE) Followed during a Long Period of Time.

Jacqueline Conard, PhD, Christophe Marzac, MD, Fabrice Juin, PhD, Marie-Helene Horellou, MD, Ors’Antone Calendini, MD, Nicole Casadevall, MD

Blood (2006) 108 (11): 4092.

https://doi.org/10.1182/blood.V108.11.4092.4092

Published: 2006

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

Protein S Gla-domain mutations causing impaired Ca 2+ -induced phospholipid binding and severe functional protein S deficiency

Suely M. Rezende, David A. Lane, Blandine Mille-Baker, Michel M. Samama, Jacqueline Conard, Rachel E. Simmonds

Blood (2002) 100 (8): 2812–2819.

https://doi.org/10.1182/blood-2002-03-0909

Published: 2002

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

Endogenous Thrombin Potential (ETP) in Patients with Hereditary Antithrombin (AT) Deficiency or Carriers of the Prothrombin (PT) 20210A Gene Mutation.

JAK2 V617F in 3 Patients with Venous Thromboembolism (VTE) Followed during a Long Period of Time.

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.

Protein S Gla-domain mutations causing impaired Ca 2+ -induced phospholipid binding and severe functional protein S deficiency

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

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ASH Publications

American Society of Hematology

Endogenous Thrombin Potential (ETP) in Patients with Hereditary Antithrombin (AT) Deficiency or Carriers of the Prothrombin (PT) 20210A Gene Mutation.

JAK2 V617F in 3 Patients with Venous Thromboembolism (VTE) Followed during a Long Period of Time.

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.

Protein S Gla-domain mutations causing impaired Ca 2+ -induced phospholipid binding and severe functional protein S deficiency

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

Email alerts

ASH Publications

American Society of Hematology

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