C3 glomerulopathy: consensus report

@inproceedings{Pickering2013C3GC,
  title={C3 glomerulopathy: consensus report},
  author={Matthew C Pickering and Vivette D D'agati and Carla M Nester and Richard J. H. Smith and Mark L. Haas and Gerald B. Appel and Charles Edward Alpers and Ingeborg M. Bajema and Camille L. Bedrosian and Michael C Braun and Mittie Doyle and Fadi Fakhouri and Fernando C Fervenza and Agnes B. Fogo and V{\'e}ronique Fr{\'e}meaux-Bacchi and Daniel P Gale and Elena Jorge and Glenn Griffin and Claire Louise Harris and Vernon Michael Holers and Sally M. Johnson and Peter Lavin and Nicholas Medjeral-Thomas and B. Paul Morgan and Cynthia C. Nast and Laure-H{\'e}l{\'e}ne Noel and Dr T. K. Peters and Santiago Rodr{\'i}guez de C{\'o}rdoba and Aude Servais and Sanjeev Sethi and Won Chol Song and Paul Tamburini and Joshua M Thurman and Michael Zavros and H Terence Cook},
  booktitle={Kidney international},
  year={2013}
}
C3 glomerulopathy is a recently introduced pathological entity whose original definition was glomerular pathology characterized by C3 accumulation with absent or scanty immunoglobulin deposition. In August 2012, an invited group of experts (comprising the authors of this document) in renal pathology, nephrology, complement biology, and complement therapeutics met to discuss C3 glomerulopathy in the first C3 Glomerulopathy Meeting. The objectives were to reach a consensus on: the definition of… CONTINUE READING
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