Results 101 to 110 of about 217,483 (203)

C3 Glomerulonephritis Presenting With Nephritic and Nephrotic Syndromes: Spontaneous Remission After Six Months on Dialysis. [PDF]

Cureus, 2023
Gonçalves F, Marques N, Silva R, Mendonça L, Faria B.   +4 more
europepmc   +1 more source

Successful simultaneous liver-kidney transplantation for renal failure associated with hereditary complement C3 deficiency.

, 2020
Hereditary complement C3 deficiency is associated with recurrent bacterial infections and proliferative glomerulonephritis. We describe a case of an adult with complete deficiency of complement C3 due to homozygous mutations in C3 gene: c.1811delT ...
Delaney, Michael, Marchbank, Kevin J, Heaton, Nigel, Nayagam, Jeremy S, Nayagam, Jeremy S., Pickering, Matthew C., Sacks, Steven H, Cairns, Tom D., Cook, H. Terry, Pickering, Matthew C, Denton, Harriet, Cook, H Terry, Montasser, Mahmoud, Shah, Sapna, Marchbank, Kevin J., Cairns, Tom D, Suddle, Abid, McGrath, Samuel, Yang, Yi, Sacks, Steven H.; id_orcid   +19 more
core   +1 more source

IgA-codominant Post-streptococcal Glomerulonephritis in a Patient with Type 1b Abernethy Malformation: A New Insight into the Pathogenesis

Medical Journal of Dr. D.Y. Patil Vidyapeeth
Post-streptococcal glomerulonephritis is an immune complex-mediated glomerulonephritis as a result of transient dysregulation of alternate complement pathway along with in situ immune complex formation.
Shashank M. Shivanna, Umesha Lingaraj, Kishan Aralapuram, Bhushan C. Shetty, C. G. Sreedhara   +4 more
doaj   +1 more source

Glomerulonephritis with isolated C3 deposits and monoclonal gammopathy: a fortuitous association?

, 2011
International audienceBACKGROUND AND OBJECTIVES: Glomerular deposition of monoclonal Ig has been exceptionally described as the cause of membranoproliferative glomerulonephritis, through activation of the complement alternative pathway (CAP).
Christine Fen Chong, Lacombe, Corinne, Frémeaux-Bacchi, Véronique, Nathalie Quellard, Jean-Marc Gombert, Véronique Frémeaux-Bacchi, Desport, Estelle, Bridoux, Franck, Touchard, Guy, Gombert, Jean-Marc, Estelle Desport, Frank Bridoux, Guy Touchard, Quellard, Nathalie, Chong, Christine Fen, Corinne Lacombe   +15 more
core   +1 more source

Eculizumab in C3 Glomerulopathy: A Systematic Review of Therapeutic Efficacy and Clinical Outcomes

Pharmaceutics
Background: C3 glomerulopathies (C3G), including dense deposit disease (DDD) and C3 glomerulonephritis (C3GN), are rare kidney disorders driven by dysregulation of the alternative complement pathway.
Dominik Lewandowski, Mateusz Konieczny, Krzysztof Chrzanowski, Marta Jakubowska, Zuzanna Paryzek, Miłosz Miedziaszczyk, Ilona Idasiak-Piechocka   +6 more
doaj   +1 more source

Renal injury in scleromyxoedema due to monoclonal gammopathy associated C3 glomerulonephritis. [PDF]

BMJ Case Rep, 2022
Kao S, Silinsky Krupnikova SD, AlMackenzie M, Atefi G.   +3 more
europepmc   +1 more source

Primary immune complex membranoproliferative glomerulonephritis and C3 glomerulonephritis: experience of two rare diseases from a single centre

Background: This study has been conducted to evaluate and compare the clinicopathological profile and treatment outcome of primary immune complex membranoproliferative glomerulonephritis (IC-MPGN) and C3 glomerulonephritis (C3 GN), two rare glomerular ...
Barai, Tonmay, Bhatttacharjee, Koushik, Dasgupta, Sanjay, Basu, Keya   +3 more
core   +1 more source

Pathogenesis and approaches to therapy of membranoproliferative glomerulonephritis

, 1976
In 1965, it was observed that patients with glomerulonephritis with persistently low serum concentrations of C3 evolved to have similar glomerular morphologic characteristics, particularly recognizable in biopsy specimens stained by the Jones methenamine
West, Clark D., Clark D. West
core   +1 more source

Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation

, 2011
Complement factor H (CFH) is a regulator of the alternative complement activation pathway. Mutations in the CFH gene are associated with atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis type II and C3 glomerulonephritis. Here,
Marquart, H V, Zipfel, P, Schmidt, I M, C B Andersen, Kirchhoff, Eva Maria, P Zipfel, Schejbel, L, M Kirchhoff, P Garred, Andersen, C B, H V Marquart, Garred, P, I M Schmidt, L Schejbel   +13 more
core   +1 more source

C3 glomerulonephritis associated with ANCA positivity: a case report. [PDF]

BMC Nephrol, 2021
Li L, Liu LQ, Yang YY, Hu ZX.
europepmc   +1 more source