The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge
Author:
Affiliation:
1. Department of Medicine, First Chair of Internal Medicine; University of Padua Medical School; Padua Italy
Funder
MURST
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.13159/fullpdf
Reference29 articles.
1. Biochemistry and genetics of von Willebrand factor;Sadler;Annu Rev Biochem,1998
2. Effect of multimeric structure of the factor VIII/von Willebrand factor protein on binding to platelets;Gralnick;Blood,1981
3. Von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interaction with platelet glycoprotein Ib;Fujimura;J Biol Chem,1986
4. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand factor;Sadler;J Thromb Haemost,2006
5. Variant von Willebrand's disease type B - revisited;Howard;Blood,1982
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