Results 31 to 40 of about 27,104 (199)

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

Development of crescentic membranoproliferative glomerulonephritis after COVID-19 vaccination [PDF]

open access: yes, 2022
Membranoproliferative glomerulonephritis (MPGN) comprises a histologic pattern of glomerular injury with different underlying diseases. Here we report on a 47-year-old female with rapidly progressive glomerulonephritis (RPGN) on top of a previously ...
Säemann, Marcus D   +5 more
core   +2 more sources

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

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

Retinal obliterative vasculitis associated to contralateral retinal neovascularization in membranoproliferative glomerulonephritis

open access: yes, 2021
Purpose: To report our experience with a peculiar case of asynchronous bilateral retinal vascular occlusion in a patient suffering from membranoproliferative glomerulonephritis.
Danieli L.   +6 more
core   +1 more source

Cryoglobulinemic Glomerulonephritis: A Case Report

open access: yesSiriraj Medical Journal, 2017
Cryoglobulinemic glomerulonephritis (CG) is rare in children. We report a 13-year-old Thai boy who presented with acute nephrotic nephritis syndrome, arthralgia, and purpura. Renal pathology revealed membranoproliferative glomerulonephritis and CG.
Nuntawan Piyaphanee
doaj   +3 more sources

Anaerococcus urinomassiliensis sp. nov., isolated from a urine sample of a 17-year-old boy affected by autoimmune hepatitis and membranoproliferative glomerulonephritis

open access: yesNew Microbes and New Infections, 2016
We report the main characteristics of ‘Anaerococcus urinomassiliensis’ strain FC4T (CSURP2143) that was isolated from a urine sample of a 17-year-old boy affected by autoimmune hepatitis and membranoproliferative glomerulonephritis.
A. Morand   +6 more
doaj   +1 more source

Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritis [PDF]

open access: yes, 2011
A 4-year-old boy presented with proteinuria and developed progressive renal failure over 6 years. In the patient's family, five individuals were affected with atypical haemolytic uraemic syndrome (aHUS) but not the patient.
Leh, Sabine   +20 more
core   +1 more source

Home - About - Disclaimer - Privacy