Complement Gene Variants and Shiga Toxin–Producing Escherichia coli–Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study

BACKGROUND AND OBJECTIVES: Inherited complement hyperactivation is critical for the pathogenesis of atypical hemolytic uremic syndrome (HUS) but undetermined in postdiarrheal HUS. Our aim was to investigate complement activation and variants of complement genes, and their association with disease se...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Clin J Am Soc Nephrol
Egile Nagusiak: Frémeaux-Bacchi, Véronique, Sellier-Leclerc, Anne-Laure, Vieira-Martins, Paula, Limou, Sophie, Kwon, Theresa, Lahoche, Annie, Novo, Robert, Llanas, Brigitte, Nobili, François, Roussey, Gwenaëlle, Cailliez, Mathilde, Ulinski, Tim, Deschênes, Georges, Alberti, Corinne, Weill, François-Xavier, Mariani, Patricia, Loirat, Chantal
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society of Nephrology 2019
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6419292/
https://ncbi.nlm.nih.gov/pubmed/30674459
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.05830518
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