Von Willebrand's disease: case report and review of literatu…
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- DOI 10.11604/pamj.2017.27.147.12248
- PMID https://pubmed.ncbi.nlm.nih.gov/28904675
- PMCID https://www.ncbi.nlm.nih.gov/pmc/articles/5567960
- OpenAlex ID W2724568528
- Type Article
- Language EN
- Published 01 Jan 2017
- Volume 27
- Pages 147
- Source Pan African Medical Journal
- Publisher African Field Epidemiology Network
- FWCI 2.11
- Countries 1
- Institutions 1
- Added 14 Jul 2017
- Updated 28 Oct 2026
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Von Willebrand's disease: case report and review of literature
Article 2017 EN Gold
Von Willebrand Disease (VWD) is the most common human inherited bleeding disorder due to a defect of Von Willebrand Factor (VWF), which a glycoprotein crucial for platelet adhesion to the subendothelium after vascular injury. VWD include quantitative defects of VWF, either partial (type 1 with VWF levels < 50 IU/dL) or virtually total (type 3 with undetectable VWF levels) and also qualitative defe…
31
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20
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5
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2.11
FWCI
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UN Sustainable Development Goals
1 SDGsAuthors & Affiliations
5 authors| # | Author | Institutions | ORCID |
|---|---|---|---|
| 1 | Hanae Echahdi | Mohammed V University (MA) | — |
| 2 | Brahim El Hasbaoui Corresponding | Mohammed V University (MA) | — |
| 3 | Mohamed El Khorassani | Mohammed V University (MA) | — |
| 4 | Aomar Agadr | Mohammed V University (MA) | — |
| 5 | Mohamed Khattab | Mohammed V University (MA) | — |
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