Coagulation factor V G allele and HR2 haplotype-Reference-Cited by-同舟云学术

Coagulation factor V G allele and HR2 haplotype

Published:2003-01 Issue:1 Volume:14 Page:49-56
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:Blood Coagulation & Fibrinolysis

Author:

Kostka Heike,Schwarz Thomas,Schellong Sebastian,Mix Cornelia,Kuhlisch Eberhard,Temelkova-Kurktschiev Theodora,Henkel Elena,Köhler Carsta,Gehrisch Siegmund,Siegert Gabriele

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference36 articles.

1. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.

2. Anticoagulant protein C pathway defective in majority of thrombophilic patients [see comments]

3. Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

4. Resistance to Activated Protein C as a Basis for Venous Thrombosis

5. The prevalence of poor anticoagulant response to activated protein C (APC resistance) among patients suffering from stroke or venous thrombosis and among healthy subjects

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1. F5‐Atlanta : A novel mutation in F5 associated with enhanced East Texas splicing and FV‐short production;Journal of Thrombosis and Haemostasis;2021-05-20

2. Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls;European Journal of Epidemiology;2013-07-31

3. The genetics of venous thromboembolism;Thrombosis and Haemostasis;2009

4. Factor V HR2 haplotype: a risk factor for venous thromboembolism in individuals with absence of Factor V Leiden;Annals of Hematology;2008-07-25

5. Combined Thrombophilic Mutations in Women with Unexplained Recurrent Miscarriage;American Journal of Reproductive Immunology;2007-02