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Von Willebrand's disease: case report and review of literature
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 l...
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| Publicat a: | Pan Afr Med J |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The African Field Epidemiology Network
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5567960/ https://ncbi.nlm.nih.gov/pubmed/28904675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.27.147.12248 |
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