Combined hereditary factor XI (plasma thromboplastin antecedent) deficiency, von Willebrand's disease, and xeroderma pigmentosum in a Japanese family
Author:
Publisher
Wiley
Subject
Hematology
Reference21 articles.
1. The Mode of Inheritance of PTA Deficiency: Evidence for the Existence of Major PTA Deficiency and Minor PTA Deficiency
2. Heredity and Coagulation Studies in Ten Families with Factor XI (Plasma Thromboplastin Antecedent) Deficiency
3. Comparison of bleeding tendency, factor XI coagulant activity, and factor XI antigen in 25 factor XI-deficient kindreds
4. von Willebrand factor and von Willebrand disease [published erratum appears in Blood 1988 Mar;71(3):830]
5. The Effect of Combined Factor XI Deficiency with von Willebrand Factor Abnormalities on Haemorrhagic Diathesis
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1. Familial multiple coagulation factor deficiencies - chance associations and distinct clinical disorders;Haemophilia;2009-01
2. Use of Recombinant Factor VIIa in Inherited and Acquired von Willebrand Disease;Clinical and Applied Thrombosis/Hemostasis;2007-12-26
3. Multiple congenital coagulopathies co-expressed with Von Willebrand’s disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature;Haemophilia;2007-11
4. Familial multiple coagulation factor deficiencies: new biologic insight from rare genetic bleeding disorders;Journal of Thrombosis and Haemostasis;2004-08-26
5. VON WILLEBRAND DISEASE IN CHILDREN AND ADOLESCENTS;Pediatric Clinics of North America;1996-06
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