Results 281 to 290 of about 102,475 (311)

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

Assembly Mechanism of Mucin and von Willebrand Factor Polymers

Cell, 2020
Gabriel Javitt, Lev Khmelnitsky, Lavi S Bigman   +2 more
exaly  

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

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

Factor-VIII/Von Willebrand factor/Von Willebrand factor

Reactions Weekly, 2015
openaire   +1 more source

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

Circulation, 2007
James C Gilbert, Robert G Schaub
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
J E Sadler, Jeroen Eikenboom
exaly  

von Willebrand disease and von Willebrand factor

Thrombosis Research, 1993
openaire   +1 more source

Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract

Gastroenterology, 2001
A Veyradier, Martine Wolf, Bernadette Obert   +2 more
exaly  

von Willebrand disease

Genetics in Medicine, 2011
Paula D James, A C Goodeve
exaly