Results 121 to 130 of about 17,249 (148)

Disseminated Bartonellosis Masquerading as Autoimmune Glomerulonephritis: A Case Report. [PDF]

Case Rep Nephrol
Debyser T, Falter M, Vanhoutte T, Koshy P, Depypere M, De Vusser K, Henckaerts L.   +6 more
europepmc   +1 more source

A very rare cause of oliguric acute kidney disease: crescentic C3 glomerulopathy. [PDF]

Oxf Med Case Reports
Kaynar K, Güven A, Gençcelep B, Ertekin T, Mungan SA.   +4 more
europepmc   +1 more source

Full-house nephropathy associated with mantle cell lymphoma. [PDF]

CEN Case Rep
Kinoshita K, Koga K, Yahata K.
europepmc   +1 more source

Congophilic fibrillary glomerulonephritis recurrence post-renal transplant: diagnostic challenges and proteomic insights. [PDF]

CEN Case Rep
Watanabe H, Nagamine M, Shintani-Domoto Y, Kawanishi K, Ishino K, Nakamura T, Sumiyoshi S, Konishi E.   +7 more
europepmc   +1 more source

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Membranoproliferative Glomerulonephritis und C3‑Glomerulopathie

Der Internist, 2019
Based on an increasingly better pathophysiological understanding over the last 10 years, in 2010 a new classification of glomerulonephritis with dominant or codominant C3 deposits was introduced and the predominant subgoup was termed C3 glomerulopathy (C3G). In the current classification, immune complex mediated membranoproliferative glomerulonephritis
B, Hohenstein, K, Amann, J, Menne
openaire   +2 more sources

Eculizumab in post-transplant C3 glomerulonephritis caused by a C3 mutation

Clinical Nephrology, 2020
C3 glomerulonephritis (C3GN) is a disorder of excess alternative complement activation leading to glomerular injury. Following kidney transplantation, C3GN has a high recurrence rate, and the overall prognosis is poor without treatment. However, treatment efficacy is highly variable.
Joon S, Kim, Kirk W, Foster, Scott G, Westphal   +2 more
openaire   +2 more sources

Alternate C3 pathway activation in pneumococcal glomerulonephritis

The American Journal of Medicine, 1975
Glomerulonephritis following pneumococcal infection has been observed, but possible immunopathologic mechanisms have not been adequately explored. Multiple serologic studies as well as light, immunofluorescence and electron microscopic evaluation of kidney biopsy tissue from a 4 year old girl with pneumococcal glomerulonephritis were performed ...
L R, Hyman, E H, Jenis, G S, Hill, S W, Zimmerman, P M, Burkholder   +4 more
openaire   +2 more sources

C3 glomerulonephritis with a severe crescentic phenotype

Pediatric Nephrology, 2017
C3 glomerulopathy (C3G) is rare type of glomerulonephritis resulting from the glomerular deposition of C3 due to dysregulation of the alternative pathway of complement. It is further subdivided into C3 glomerulonephritis (C3GN) and dense deposit disease (DDD), depending on the ultrastructural features. C3GN usually presents with a membranoproliferative
Aishwarya Ravindran, Fernando C. Fervenza, Richard J. H. Smith, Sanjeev Sethi   +3 more
openaire   +2 more sources