Results 251 to 260 of about 31,578 (263)

First-in-Human Evaluation of Anti–von Willebrand Factor Therapeutic Aptamer ARC1779 in Healthy Volunteers

Circulation, 2007
James Gilbert, Robert G Schaub
exaly  

Acquired von Willebrand syndrome: An update

American Journal of Hematology, 2007
Massimo Franchini
exaly  

Serum concentrations of von Willebrand factor and soluble thrombomodulin indicate alteration of endothelial function in inflammatory bowel diseases

Digestive Diseases and Sciences, 1995
A M Sawyerr, A J Wakefield, Hall A
exaly  

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 about
openaire   +1 more source

Variability of von Willebrand factor‐related parameters in endothelial colony forming cells

Journal of Thrombosis and Haemostasis, 2019
Annika De Jong, Richard Dirven, Jeroen Eikenboom   +2 more
exaly  

von Willebrand disease and von Willebrand factor

Thrombosis Research, 1993
openaire   +1 more source

Acquired von Willebrand syndrome: Features and management

American Journal of Hematology, 2006
exaly  

von Willebrand Disease and von Willebrand Factor

Clinics in Laboratory Medicine
Bailey Hutchison, Andrew Podd, Sandra L. Haberichter   +2 more
openaire   +1 more source

Mitral regurgitation is associated with similar loss of von Willebrand factor large multimers but lower frequency of anemia compared with aortic stenosis

Research and Practice in Thrombosis and Haemostasis
Genichi Sakaguchi, Michiya Hanyu
exaly  

von Willebrand disease-specific defects and proteomic signatures in endothelial colony–forming cells

Journal of Thrombosis and Haemostasis
Frank Leebeek, Sebastiaan Laan, Wala Al Arashi   +2 more
exaly