Molecular mechanism and classification of von Willebrand disease.

Abstract:

:The characterization of mutations in von Willebrand disease provides useful insight into the synthesis, structure, and function of von Willebrand factor. This growing body of information has prompted a reclassification of vWD types that is intended to reflect distinct pathophysiologic mechanisms. Despite this apparent progress, many aspects of vWF biology and pathophysiology remain poorly understood. These include the mechanism by which binding of vWF to platelets is induced at sites of vascular injury, and the factors that influence the likelihood of bleeding symptoms in patients with vWD type 1.

journal_name

Thromb Haemost

authors

Sadler JE,Matsushita T,Dong Z,Tuley EA,Westfield LA

subject

Has Abstract

pub_date

1995-07-01 00:00:00

pages

161-6

issue

1

eissn

0340-6245

issn

2567-689X

journal_volume

74

pub_type

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