Glomerular Complement Factor H–Related Protein 5 (FHR5) Is Highly Prevalent in C3 Glomerulopathy and Associated With Renal Impairment
Author:
Funder
Wellcome Trust
Kidney Research UK
Publisher
Elsevier BV
Subject
Nephrology
Reference39 articles.
1. C3 glomerulopathy: consensus report;Pickering;Kidney Int,2013
2. Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference;Goodship;Kidney Int,2017
3. The renaissance of complement therapeutics;Ricklin;Nat Rev Nephrol,2018
4. Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies;Servais;Kidney Int,2012
5. C3 glomerulonephritis and dense deposit disease share a similar disease course in a large United States cohort of patients with C3 glomerulopathy;Bomback;Kidney Int,2018
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