Results 11 to 20 of about 17,249 (148)

WCN24-386 C3 GLOMERULONEPHRITIS AND C3-DOMINANT INFECTION RELATED GLOMERULONEPHRITIS - ARE THEY SIMILAR?

open access: yesKidney International Reports
Mythri Shankar   +4 more
doaj   +2 more sources

Primary membranoproliferative glomerulonephritis: natural history, pathogenesis, and treatment [PDF]

open access: yesFrontiers in Nephrology
Primary membranoproliferative glomerulonephritis (MPGN) is an ultrarare disease characterized by immunofluorescence microscopy as either immune-complex mediated (IC-MPGN) or C3 glomerulopathy (C3), the latter subdivided by electron microscopy to C3 ...
Edward J. Filippone, John L. Farber
doaj   +2 more sources

C3 glomerulonephritis: a new category of glomerulonephritis with etiopathogenic implications

open access: yesIatreia, 2015
Introduction: Glomerulonephritis with only deposits of C3 (GN-C3) could involve alteration on the complement alternative pathway.Objective: To describe retrospectively a series of GNC3 cases and to determine the frequency with which patients continue ...
Taborda Murillo, Alejandra   +2 more
doaj   +1 more source

C3 Glomerulonephritis Associated with Monoclonal Gammopathy of Renal Significance

open access: yesActa Médica Portuguesa, 2021
Introduction: Monoclonal gammopathy of renal significance (MGRS) is described as a hematologic condition characterized by nephrotoxic monoclonal proteins produced by a non-malignant B-cell or plasma cell clone. Nevertheless, MGRS can cause serious renal
Inês Gomes-Alves, Inês Castro-Ferreira
doaj   +1 more source

Pathology of C3 Glomerulopathy [PDF]

open access: yesChildhood Kidney Diseases, 2019
C3 glomerulopathy is a renal disorder involving dysregulation of alternative pathway complement activation. In most instances, a membranoproliferative pattern of glomerular injury with a prevalence of C3 deposition is observed by immunofluorescence ...
Su-Jin Shin, Yoonje Seong, Beom Jin Lim
doaj   +1 more source

Eculizumab and recurrent C3 glomerulonephritis [PDF]

open access: yesPediatric Nephrology, 2013
Hyperactivity of the alternative complement pathway is the principle defect in C3 glomerulopathies (C3G). Eculizumab, a monoclonal antibody that binds C5 to prevent formation of the membrane attack complex, has been shown to be beneficial in some patients with this disease.In this open-label, proof-of-concept efficacy-and-safety study, a patient with ...
Sevgi, Gurkan   +5 more
openaire   +2 more sources

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

Heterozygous laminin β2 mutation in C3 glomerulopathy

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2021
C3 glomerulopathy is usually seen with the presence of C3 nephritic factor, homozygous or heterozygous mutations in the regulatory complement proteins factor H, factor I, or C3. We describe the presence of heterozygous laminin β2 mutation in a patient of
Manish R Balwani   +3 more
doaj   +1 more source

C3 glomerulonephritis and CFHR5 nephropathy [PDF]

open access: yesNephrology Dialysis Transplantation, 2012
Complement is an important aspect of defence against infection and its activation and regulation are finely balanced. Disordered complement regulation can lead to C3 glomerulonephritis (C3GN), which is characterized by complement (but not immunoglobulin) deposition in the glomerulus of the kidney. Although only recently recognized as a clinical entity,
Daniel P, Gale, Patrick H, Maxwell
openaire   +2 more sources

A novel mutation in complement 2 accompanied by susceptibility variants in C3 glomerulonephritis: A case study

open access: yesNefrología (English Edition), 2019
Background: C3 glomerulonephritis is a rare, chronic disease characterized by C3c-dominant staining on renal biopsy and is caused by inherited or acquired alternative complement pathway dysregulation.
Sha-sha Han   +5 more
doaj   +3 more sources

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