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Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
Central to the pathogenesis of atypical haemolytic uraemic syndrome (aHUS) is over-activation of the alternative pathway of complement. Inherited defects in complement genes and autoantibodies against complement regulatory proteins have been described. The use of plasma exchange to replace non-funct...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Pergamon Press
2013
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3899040/ https://ncbi.nlm.nih.gov/pubmed/23810412 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molimm.2013.05.224 |
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