C3 glomerulonephritis and dense deposit disease share a similar disease course in a large United States cohort of patients with C3 glomerulopathy
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Fakhouri, 2010, C3 glomerulopathy: a new classification, Nat Rev Nephrol, 6, 494, 10.1038/nrneph.2010.85
Servais, 2012, Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies, Kidney Int, 82, 454, 10.1038/ki.2012.63
Medjeral-Thomas, 2014, C3 glomerulopathy: clinicopathologic features and predictors of outcome, Clin J Am Soc Nephrol, 9, 46, 10.2215/CJN.04700513
Bomback, 2012, Pathogenesis of the C3 glomerulopathies and reclassification of MPGN, Nat Rev Nephrol, 8, 634, 10.1038/nrneph.2012.213
Hou, 2014, Toward a working definition of C3 glomerulopathy by immunofluorescence, Kidney Int, 85, 450, 10.1038/ki.2013.340
Zhang, 2012, Causes of alternative pathway dysregulation in dense deposit disease, Clin J Am Soc Nephrol, 7, 265, 10.2215/CJN.07900811
Okuda, 2015, Membranoproliferative glomerulonephritis and C3 glomerulonephritis: frequency, clinical features, and outcome in children, Nephrology (Carlton), 20, 286, 10.1111/nep.12382
Rabasco, 2015, Effectiveness of mycophenolate mofetil in C3 glomerulonephritis, Kidney Int, 88, 1153, 10.1038/ki.2015.227
Caliskan, 2017, Immunosuppressive treatment in C3 glomerulopathy: is it really effective?, Am J Nephrol, 46, 96, 10.1159/000479012
Iatropoulos, 2016, Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome, Mol Immunol, 71, 131, 10.1016/j.molimm.2016.01.010
Zand, 2013, C3 glomerulonephritis associated with monoclonal gammopathy: a case series, Am J Kidney Dis, 62, 506, 10.1053/j.ajkd.2013.02.370
Chauvet, 2017, Treatment of B-cell disorder improves renal outcome of patients with monoclonal gammopathy-associated C3 glomerulopathy, Blood, 129, 1437, 10.1182/blood-2016-08-737163
Sethi, 2012, C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up, Kidney Int, 82, 465, 10.1038/ki.2012.212
Coppo, 2014, Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments, Kidney Int, 86, 828, 10.1038/ki.2014.63
Richards, 2015, Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology, Genet Med, 17, 405, 10.1038/gim.2015.30
Goodship, 2017, Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference, Kidney Int, 91, 539, 10.1016/j.kint.2016.10.005
Levey, 2009, A new equation to estimate glomerular filtration rate, Ann Intern Med, 150, 604, 10.7326/0003-4819-150-9-200905050-00006
Weening, 2014, The classification of glomerulonephritis in systemic lupus erythematosus revisited, J Am Soc Nephrol, 15, 241, 10.1097/01.ASN.0000108969.21691.5D
Roberts, 2009, The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility, Kidney Int, 76, 546, 10.1038/ki.2009.168
Sethi, 2016, Mayo Clinic/Renal Pathology Society Consensus Report on Pathologic Classification, Diagnosis, and Reporting of GN, J Am Soc Nephrol, 27, 1278, 10.1681/ASN.2015060612