Predictive factors for poor outcome in pediatric C3 glomerulonephritis
Author:
Affiliation:
1. Department of Pediatrics, Fukushima Medical University School of Medicine
Publisher
The Fukushima Society of Medical Science
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/fms/64/3/64_2018-05/_pdf
Reference24 articles.
1. 1. Fakhouri F, Frémeaux-Bacchi V, Noël LH, Cook HT, Pickering MC. C3 glomerulopathy: a new classification. Nat Rev Nephrol, 6(8): 494-499, 2010.
2. 2. Martínez-Barricarte R, Heurich M, Valdes-Cañedo F, et al. Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. J Clin Invest, 120(10): 3702-3712, 2010.
3. 3. Servais A, Noël LH, Roumenina LT, et al. Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney Int, 82(4): 454-464, 2012.
4. 4. Pickering MC, D’Agati VD, Nester CM, et al. C3 glomerulopathy: consensus report. Kidney Int, 84(6): 1079-1089, 2013.
5. 5. Hou J, Markowitz GS, Bomback AS, et al. Toward a working definition of C3 Glomerulopathy by immunofluorescence. Kidney Int, 85(2): 450-456, 2014.
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