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Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome
Background and objectives: Atypical hemolytic uremic syndrome (aHUS) is associated with a congenital or acquired dysregulation of the complement alternative pathway that leads to continuous complement activation on host cells causing inflammation and damage. Eculizumab, a humanized mAb against compl...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
American Society of Nephrology
2009
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2723971/ https://ncbi.nlm.nih.gov/pubmed/19556379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.01090209 |
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