Results 171 to 180 of about 8,401,904 (201)

Inhibition of Willebrand factor in von Willebrand disease

Thrombosis Research, 1979
S, Maragall, R, Castillo, A, Ordinas, F, Liendo, M, Rodríguez   +4 more
openaire   +2 more sources

Factor-VIII/Von Willebrand factor/Von Willebrand factor

Reactions Weekly, 2015
openaire   +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 about
openaire   +1 more source

Assembly Mechanism of Mucin and von Willebrand Factor Polymers

Cell, 2020
Nadav Elad, Deborah Fass, Lev Khmelnitsky   +2 more
exaly  

von Willebrand disease and von Willebrand factor

Thrombosis Research, 1993
openaire   +1 more source

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

Circulation, 2007
James Gilbert, Robert G Schaub
exaly  

Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract

Gastroenterology, 2001
Axel Balian, Bernadette Obert, Jean-Claude Chaput   +2 more
exaly  

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Journal of Thrombosis and Haemostasis, 2006
Alok Srivastava, Pier Mannuccio Mannucci
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

Recombinant von Willebrand Factor

Thrombosis and Haemostasis, 1997
H P, Schwarz, P L, Turecek, L, Pichler, A, Mitterer, W, Mundt, F, Dorner, J, Roussi, L, Drouet   +7 more
openaire   +2 more sources