Glomerulonephritis With Isolated C3 Deposits and Monoclonal Gammopathy | Zendy

Frank Bridoux | Zendy; Éstelle Desport | Zendy; Véronique FrémeauxBacchi | Zendy; Christine Fen Chong | Zendy; JeanMarc Gombert | Zendy; Corinne Lacombe | Zendy; Nathalie Quellard | Zendy; Guy Touchard | Zendy

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Glomerulonephritis With Isolated C3 Deposits and Monoclonal Gammopathy

Author(s) -

Frank Bridoux,

Éstelle Desport,

Véronique FrémeauxBacchi,

Christine Fen Chong,

JeanMarc Gombert,

Corinne Lacombe,

Nathalie Quellard,

Guy Touchard

Publication year - 2011

Publication title -

clinical journal of the american society of nephrology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.755

H-Index - 151

eISSN - 1555-905X

pISSN - 1555-9041

DOI - 10.2215/cjn.06180710

Subject(s) - membranoproliferative glomerulonephritis , medicine , monoclonal gammopathy of undetermined significance , proteinuria , monoclonal , glomerulonephritis , properdin , plasma cell dyscrasia , pathology , nephrotic syndrome , alternative complement pathway , complement factor b , complement system , nephropathy , immunology , kidney , monoclonal antibody , endocrinology , immunoglobulin light chain , antibody , diabetes mellitus

Glomerular deposition of monoclonal Ig has been exceptionally described as the cause of membranoproliferative glomerulonephritis, through activation of the complement alternative pathway (CAP).

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