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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...
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| 出版年: | Res Pract Thromb Haemost |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2018
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| 主題: | |
| オンライン･アクセス: | 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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