Hemophilia and Von Willebrand Disease. Factor VIII Von Willebrand Factor

Hemophilia and Von Willebrand Disease. Factor VIII Von Willebrand Factor

Paperback (19 Jun 2018)

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Publisher's Synopsis

Hemophilia and Von Willebrand Disease: Factor VIII and Von Willebrand Factor serves as a must-have reference on the important role these essential blood-clotting proteins play in research and clinical medicine. Clinicians and researchers face the daily challenge of staying current on the vast amounts of research that is now generated. The reference to Janus in the title refers to the two roles of the Factor VIII/Von Willebrand Factor Complex: initiation of coagulation and propagation of clot formation. The complex prevents bleeding in hemophilia and Von Willebrand disease but also augments arterial and venous thrombosis.

Book information

ISBN: 9780128129548
Publisher: Elsevier Science
Imprint: Academic Press
Pub date:
DEWEY: 616.157
DEWEY edition: 23
Language: English
Number of pages: 286
Weight: 430g
Height: 152mm
Width: 227mm
Spine width: 15mm