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Early treatment with eculizumab in atypical haemolytic uraemic syndrome

Atypical haemolytic uraemic syndrome (aHUS) is a rare and life-threatening disease caused by complement system dysregulation leading to uncontrolled complement activation and thrombotic microangiopathy. We report the case of an adult patient with plasmaphaeresis-resistant aHUS and hypertension treat...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Kidney J
Prif Awduron: Garjau, Maria, Azancot, María, Ramos, Rosa, Sánchez-Corral, Pilar, Montero, Maria Angeles, Serón, Daniel
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2012
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4400458/
https://ncbi.nlm.nih.gov/pubmed/26069743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndtplus/sfr157
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