Von Willebrand Disease: An Update
Emerging
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- DOI 10.4172/2155-9864.1000238
- OpenAlex ID W2338188334
- Type Article
- Language DE
- Published 01 Jan 2014
- Volume 05 (09)
- Source Journal of Blood Disorders & Transfusion
- Publisher OMICS Publishing Group
- FWCI 0.71
- Countries 1
- Institutions 4
- Added 24 Jun 2016
- Updated 12 Oct 2026
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Von Willebrand Disease: An Update
Article 2014 DE Hybrid
Von Willebrand disease (VWD) is a common hereditary bleeding disorder, inherited either as an autosomally dominant or recessive trait.It is caused by a quantitative and/ or qualitative defect in the Von Willebrand Factor (VWF) which plays two critical roles in hemostasis i.e., platelet adhesion and aggregation to damaged endothelium, and also as a carrier for Factor VIII (FVIII) molecule which sta…
6
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59
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1
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0.71
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1 SDGsAuthors & Affiliations
1 authors| # | Author | Institutions | ORCID |
|---|---|---|---|
| 1 | Dipika Mohanty Corresponding | Apollo Hospitals (IN) Apollo Hospitals (IN) +2 | — |
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