Laboratory diagnosis of von Willebrand disease

Author:

Roberts J. C.1,Flood V. H.23

Affiliation:

1. Bleeding & Clotting Disorders Institute; Peoria IL USA

2. Division of Hematology/Oncology; Department of Pediatrics; Medical College of Wisconsin; Milwaukee WI USA

3. Children's Research Institute; Children's Hospital of Wisconsin; Milwaukee WI USA

Funder

National Institutes of Health

MACC Fund (Midwest Athletes Against Childhood Cancer)

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference23 articles.

1. Von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein ib;Fujimura;J Biol Chem,1986

2. Isolation and characterization of two domains of human von Willebrand factor that interact with fibrillar collagen types I and III;Pareti;J Biol Chem,1987

3. A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor;Foster;J Biol Chem,1987

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. Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the european multicenter study MCMDM-1VWD;Castaman;Thromb Res,2010

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