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Pathophysiology of thrombotic thrombocytopenic purpura
The discovery of a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) revolutionized our approach to thrombotic thrombocytopenic purpura (TTP). Inherited or acquired ADAMTS13 deficiency allows the unrestrained growth of microthrombi that are composed of von...
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| Publicat a: | Blood |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Hematology
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5606001/ https://ncbi.nlm.nih.gov/pubmed/28768626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2017-04-636431 |
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