Risk of Major Bleeding with Antiplatelet and/or Anticoagulation Therapy in Inherited Factor XI Deficiency: Insights from Real-World Observations-Reference-Cited by-同舟云学术

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Risk of Major Bleeding with Antiplatelet and/or Anticoagulation Therapy in Inherited Factor XI Deficiency: Insights from Real-World Observations

Published:2024-06-18 Issue: Volume: Page:
ISSN:0340-6245
Container-title:Thrombosis and Haemostasis
language:en
Short-container-title:Thromb Haemost

Author:

Vaismann Shanni,Stein Nili¹,Dizengoff Liat²,Warwar Amir,Perek Shoshan²,Zoabi Ibraheem²,Saliba Walid,Preis Meir

Affiliation:

1. Department of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, Haifa, Israel

2. Institute of Hematology, Lady Davis Carmel Medical Center, Haifa, Israel

Publisher

Georg Thieme Verlag KG

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-2347-4338.pdf

Reference9 articles.

1. 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;O Shpilberg;Blood,1995

2. Factor XI deficiency in humans;U Seligsohn;J Thromb Haemost,2009

3. Factor XI activation in a revised model of blood coagulation;D Gailani;Science,1991

4. Thrombin-mediated activation of factor XI results in a thrombin-activatable fibrinolysis inhibitor-dependent inhibition of fibrinolysis;P A Von dem Borne;J Clin Invest,1997

5. Variable bleeding manifestations characterize different types of surgery in patients with severe factor XI deficiency enabling parsimonious use of replacement therapy;O Salomon;Haemophilia,2006

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