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Hereditary angioedema: Linking complement regulation to the coagulation system
Congenital deficiency of C1 inhibitor, the main inhibitor of the classic complement system pathway, leads to paroxysmal angioedema (hereditary angioedema) that can be debilitating or life‐threatening for affected patients. In the past few years many new insights on the pathogenesis of angioedema for...
Uloženo v:
| Vydáno v: | Res Pract Thromb Haemost |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6332742/ https://ncbi.nlm.nih.gov/pubmed/30656274 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rth2.12175 |
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