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...

Full description

Saved in:
Bibliographic Details
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
Format: Artigo
Language:Inglês
Published: American Society of Nephrology 2014
Subjects:
Original Articles
Online Access: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
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items