Associated Papers
Diseases of complement dysregulation-an overview.
Wong EKS et al.
Seminars in Immunopathology, 2018
Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case.
Gnappi E et al.
Pediatric Nephrology (berlin, Germany), 2012
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.
Servais A et al.
Kidney International, 2012
Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation.
Leroy V et al.
Pediatric Nephrology (berlin, Germany), 2011
A novel mutation in complement 2 accompanied by susceptibility variants in C3 glomerulonephritis: A case study.
Han SS et al.
Nefrologia, 0
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