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Autor:
Olivia May, Nicolas S. Merle, Anne Grunenwald, Viviane Gnemmi, Juliette Leon, Cloé Payet, Tania Robe-Rybkine, Romain Paule, Florian Delguste, Simon C. Satchell, Peter W. Mathieson, Marc Hazzan, Eric Boulanger, Jordan D. Dimitrov, Veronique Fremeaux-Bacchi, Marie Frimat, Lubka T. Roumenina
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Atypical hemolytic uremic syndrome (aHUS) is a severe disease characterized by microvascular endothelial cell (EC) lesions leading to thrombi formation, mechanical hemolysis and organ failure, predominantly renal. Complement system overactivation is
Externí odkaz:
https://doaj.org/article/ab3a68c47e3c4970883cff46cc2fc1af
