Type IIB von Willebrand's disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.00285.x-i1/fullpdf
Reference25 articles.
1. Factor VIII on the vascular intima: possible importance in haemostasis and thrombosis;Bloom;Nature; New Biology,1973
2. Familial occurrence of von Willebrand's disease, thrombocytopenia, severe gastrointestinal bleeding;Corder;American Journal of Medical Sciences,1973
3. Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein IIb induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation;DeMarco;Proceedings of the National Academy of Sciences of the United States of America,1985
4. von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor;Gralnick;Journal of Clinical Investigation,1985
5. von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma;Holmberg;Blood,1986
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