Smith RJH, et al. C3 glomerulopathy—understanding a rare complement-driven renal disease. Nat Rev Nephrol 2019; 15:129–143. doi: 10.1038/s41581-018-0107-2
Fakhouri F, et al. Haemolytic uraemic syndrome. Lancet 2017; 390:681–696. doi: 10.1016/S0140-6736(17)30062-4
Busutti M, et al. Efficacy of eculizumab in coexisting complement C3 glomerulopathy and atypical hemolytic uremic syndrome. Kidney Int Rep 2021; 6:534–537. doi: 10.1016/j.ekir.2020.10.037
Chabannes M, et al. C3 glomerulopathy with concurrent thrombotic microangiopathy: Clinical and immunological features. Am J Kidney Dis (published online ahead of print April 13, 2023). doi: 10.1053/j.ajkd.2022.12.020; https://doi.org/10.1053/j.ajkd.2022.12.020
Ravindran A, et al. Overlap of C3 glomerulopathy and thrombotic microangiopathy: A case series. Kidney Int Rep 2022; 8:619–627. doi: 10.1016/j.ekir.2022.12.009
Merinero HM, et al. Complete functional characterization of disease-associated genetic variants in the complement factor H gene. Kidney Int 2018; 93:470–481. doi: 10.1016/j.kint.2017.07.015
McAdoo SP, et al. Patients double-seropositive for ANCA and anti-GBM antibodies have varied renal survival, frequency of relapse, and outcomes compared to single-seropositive patients. Kidney Int 2017; 92:693–702. doi: 10.1016/j.kint.2017.03.014
Schmidt T, et al. An interdisciplinary diagnostic approach to guide therapy in C3 glomerulopathy. Front Immunol 2022; 13:826513. doi: 10.3389/fimmu.2022.826513