Variable bleeding manifestations characterize different types of surgery in patients with severe factor XI deficiency enabling parsimonious use of replacement therapy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2006.01304.x/fullpdf
Reference11 articles.
1. The Mode of Inheritance of PTA Deficiency: Evidence for the Existence of Major PTA Deficiency and Minor PTA Deficiency
2. Factor XI Deficiency
3. Factor XI Deficiency in Ashkenazi Jews in Israel
4. 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 [see comments]
5. Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients
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2. Factor XIa inhibition as a therapeutic strategy for atherothrombosis;Journal of Thrombosis and Thrombolysis;2024-07-29
3. Risk of Major Bleeding with Antiplatelet and/or Anticoagulation Therapy in Inherited Factor XI Deficiency: Insights from Real-World Observations;Thrombosis and Haemostasis;2024-06-18
4. Factor XI deficiency: phenotypic age-related considerations and clinical approach towards bleeding risk assessment;Blood;2024-04-11
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