The many faces of C3 glomerulopathy

Kidney International

Volumn 82, Issue 5, 2012, Pages 611-

  Meleg Smith, Suzanne ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3; IMMUNOGLOBULIN G;

ACUTE GLOMERULONEPHRITIS; COMPLEMENT ACTIVATION; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; GLOMERULOPATHY; HUMAN; HYPOCOMPLEMENTEMIA; KIDNEY BIOPSY; LETTER; MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS; MENINGOCOCCEMIA; OUTCOME ASSESSMENT; PHENOTYPE; PRIORITY JOURNAL;

EID: 84865241316     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2012.220     Document Type: Letter

References (4)

1. Sethi S, Nexter CM, Smith RJH. Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion. Kid Int 2012; 81: 434-441.
2. Shahidi-Asl M, Ananth M, Boineau F et al. Apparent progression of acute glomerulonephritis to dense deposit disease. Ultrastr Pathol 2000; 24: 273.
3. Fakhouri F, Frémeaux-Bacchi V, Noël LH et al. C3 glomerulopathy: a new classification. Nat Rev Nephrol 2010; 6: 494-499.
4. Servais A, Frémeaux-Bacchi V, Lequintrec M et al. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. J Med Genet 2007; 44: 193-199. (Pubitemid 46580528)