Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome

BACKGROUND AND OBJECTIVES: Atypical hemolytic uremic syndrome is characterized by vascular endothelial damage caused by complement dysregulation. Consistently, complement inhibition therapies are highly effective in most patients with atypical hemolytic uremic syndrome. Recently, it was shown that a...

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Detalhes bibliográficos
Main Authors: Sánchez Chinchilla, Daniel, Pinto, Sheila, Hoppe, Bernd, Adragna, Marta, Lopez, Laura, Justa Roldan, Maria Luisa, Peña, Antonia, Lopez Trascasa, Margarita, Sánchez-Corral, Pilar, Rodríguez de Córdoba, Santiago
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2014
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4152807/
https://ncbi.nlm.nih.gov/pubmed/25135762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.01640214
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