Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
Délégation Paris 5 · Université Paris Cité · +8 more institutions
Indexed incrossrefpubmed
Abstract
No abstract available for this paper.
Citation impact
564
total citations
- FWCI
- 14.75
- Percentile
- 100%
- References
- 54
Citations per year
Authors
15- ASAude ServaisCorresponding
Délégation Paris 5, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique – Hôpitaux de Paris
- LNLaure‐Hélène Noël
Hôpital Necker-Enfants Malades, Inserm, Assistance Publique – Hôpitaux de Paris
- LTLubka T. Roumenina
Centre de Recherche des Cordeliers, Inserm
- MLMoglie Le Quintrec
Inserm, Centre de Recherche des Cordeliers
- SNStéphanie Ngo
Assistance Publique – Hôpitaux de Paris, Hôpital Européen, Hôpital Européen Georges-Pompidou
Topics & keywords
Topics
Keywords
- Membranoproliferative glomerulonephritis
- Glomerulonephritis
- Alternative complement pathway
- Factor H
- Glomerular basement membrane
- Mesangial proliferative glomerulonephritis
- Complement system
- Pathogenesis
No related works found for this paper.