Results 291 to 300 of about 157,236 (308)
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Insights from von Willebrand disease animal models
Cellular and Molecular Life Sciences, 1999Cecile Denis +2 more
exaly
Type 2M von Willebrand disease – more often misidentified than correctly identified
Haemophilia, 2016E. Favaloro +8 more
semanticscholar +1 more source
A molecular approach to the classification of von Willebrand disease
Best Practice and Research in Clinical Haematology, 2001Reinhard Schneppenheim +2 more
exaly
von Willebrand factor and von Willebrand disease.
[Rinsho ketsueki] The Japanese journal of clinical hematology, 2016T. Matsui, J. Hamako
semanticscholar +1 more source
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function
Best Practice and Research in Clinical Haematology, 2001Anne-Sophie Ribba +2 more
exaly
Treatment of von Willebrand Disease
Seminars in Thrombosis and Hemostasis, 2016J. Curnow, Leonardo Pasalic, E. Favaloro
semanticscholar +1 more source
Von Willebrand factor and von Willebrand disease
Von Willebrand disease (vWD) is an autosomally inherited bleeding disorder caused by a deficiency or abnormality of von Willebrand factor (vWF). vWF is a large multimeric glycoprotein that mediates platelet adhesion at the site of vessel injury. Also, it protects factor VIII from proteolytic degradation in the circulation. vWD has a prevalence of aboutopenaire +1 more source