Factor V Deficiency Associated with Congenital Cardiac Disorder and Intracranial Hemorrage
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-012-0149-8.pdf
Reference13 articles.
1. Asselta R, Peyvandi F (2009) Factor V deficiency. Semin Thromb Hemost 35:382–389
2. Huang JN, Koerper MA (2008) Factor V deficiency: a concise review. Haemophilia 14:1164–1169
3. Owren PA (1947) Parahaemophilia: haemorrhagic diathesis due to absence of a previously unknown clotting factor. Lancet 249:446–448
4. Shen L, He X, Dahlback B (1997) Synergistic cofactor function of factor V and protein S to activated protein C in the inactivation of the factor VIIIa–factor IXa complex–species specific interactions of components of the protein C anticoagulant system. Thromb Haemost 78:1030–1036
5. Montefusco MC, Duga S, Asselta R et al (2000) A novel two base pair deletion in the factor V gene associated with severe factor V deficiency. Br J Haematol 111:1240–1246
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical, Laboratory, and Molecular Aspects of Factor V Deficiency;Seminars in Thrombosis and Hemostasis;2024-08-27
2. Congenital coagulation factor V deficiency with intracranial hemorrhage;Journal of Clinical Laboratory Analysis;2022-09-20
3. A Novel Phenotype of the Factor 5 Gene Mutation (Homozygote Met1736Val and Heterozygote Asp68His) Is Associated With Moderate Factor V Deficiency;Frontiers in Medicine;2022-06-09
4. Association of factor V activity with risk of venous thromboembolism and atherothrombotic cardiovascular events: A retrospective population-based cohort study;Thrombosis Research;2018-08
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