TY - BOOK
T1 - Hemophilia and Von Willebrand disease
T2 - Factor VIII and Von Willebrand factor
AU - Green, David
N1 - Publisher Copyright:
© 2018 Elsevier Inc. All rights reserved.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85080821498&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85080821498&partnerID=8YFLogxK
U2 - 10.1016/C2016-0-04171-2
DO - 10.1016/C2016-0-04171-2
M3 - Book
AN - SCOPUS:85080821498
SN - 9780128129555
BT - Hemophilia and Von Willebrand disease
PB - Elsevier
ER -