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von Willebrand factor and von Willebrand disease.
[Rinsho ketsueki] The Japanese journal of clinical hematology, 2017von Willebrand factor (VWF) has two major roles in hemostasis, as a form of molecular glue which functions in platelet plug formation and as a protective transporter for coagulation factor VIII (FVIII). VWF shows a multimeric chain structure composed of 270 kDa subunits containing binding domains for FVIII, platelet and collagens. Biosynthesis, storage,
Taei, Matsui, Jiharu, Hamako
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Impact, Diagnosis and Treatment of von Willebrand Disease
Thrombosis and Haemostasis, 2000J. Sadler +9 more
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The American Journal of Medicine, 1963
M, BLOMBACK, J E, JORPES, I M, NILSSON
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M, BLOMBACK, J E, JORPES, I M, NILSSON
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Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients.
Blood Cells, Molecules & Diseases, 2003L. Baronciani +6 more
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