Hemophilia and Von Willebrand Disease
Factor VIII and Von Willebrand Factor
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25 279 Ft (24 075 Ft + 5% VAT)
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25 279 Ft
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Product details:
- Publisher Elsevier Science
- Date of Publication 19 June 2018
- ISBN 9780128129548
- Binding Paperback
- No. of pages286 pages
- Size 228x152 mm
- Weight 430 g
- Language English 0
Categories
Long description:
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.
MoreTable of Contents:
1. Historical Background2. Factor VIII: Anatomy and Physiology3. Genetic Basis of Hemophilia4. Factor VIII Therapy for Bleeding5. Complications of Therapy6. Acquired Disorders of Factor VIII7. Factor VIII and Thrombosis8. Factor VIII: Future Directions
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