Results 21 to 30 of about 9,727 (212)

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

open access: yesScientific Reports, 2020
Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N)
Shinya Ishiko   +20 more
doaj   +1 more source

Two Cases of Membranoproliferative Glomerulonephritis With Severe Proteinuria

open access: yesJournal of Behçet Uz Children's Hospital, 2019
Membranoproliferative glomerulonephritis is a common cause of chronic glomerulonephritis in older children and adolescents. Patients may present with microscopic hematuria with or without mild proteinuria with nephrotic syndrome or hypertension with ...
rahime Renda   +3 more
doaj   +1 more source

Comprehensive review of membranoproliferative glomerulonephritis: spotlighting the latest advances in revised classification and treatment [PDF]

open access: yesChildhood Kidney Diseases, 2023
Membranoproliferative glomerulonephritis (MPGN) is a complex group of renal diseases characterized by a specific pattern of glomerular injury that includes thickening of the capillary wall and mesangial expansion, leading to a heterogeneous group of ...
Jeong Yeon Kim
doaj   +1 more source

Essential mixed cryoglobulinemia type II: case report

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba, 2018
The cryoglobulinemic syndrome is produced by precipitating immunoglobulins at low temperatures. Its production is associated with several causes, such as lymphoproliferative disorders, chronic infections and autoimmune disorders. However, the etiology is
Marcos Mazzota   +6 more
doaj   +1 more source

C3 Glomerulopathy: recent advances and an update on management [PDF]

open access: yesBrazilian Journal of Nephrology
C3 glomerulopathy (C3G) is a clinicopathologic entity characterized by glomerular inflammation with dominant staining for C3 on immunofluorescence microscopy.
Lilian Monteiro Pereira Palma   +2 more
doaj   +4 more sources

Retinal findings in membranoproliferative glomerulonephritis

open access: yesAmerican Journal of Ophthalmology Case Reports, 2017
Purpose: To assess the evolution of retinal findings in patients with membranoproliferative glomerulonephritis (MPGN) by funduscopy, intravenous fluorescein angiography and optical coherence tomography. Observations: Three women and one man were followed
Ahmad M. Mansour   +6 more
doaj   +1 more source

Crescentic membranoproliferative glomerulonephritis in HIV infection; a mini-review with case study [PDF]

open access: yesJournal of Nephropathology, 2022
HIV-related renal diseases have become more evident and easier to treat due to the prolonged survival of patients with HIV infection on antiretroviral therapy (ART). There are multiple factors involved in the pathogenesis of this entity.
Priti Meena   +6 more
doaj   +1 more source

Membranoproliferative glomerulonephritis complicating Waldenström’s macroglobulinemia

open access: yesBMC Nephrology, 2012
Background Lymphoproliferative disorders causing paraproteinemia can be associated with various kidney injuries including the deposition of monoclonal immunoglobulins (Ig).
Kratochvil David   +3 more
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

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