Results 121 to 130 of about 7,623,830 (208)

Anti-glomerular basement membrane glomerulonephritis and thrombotic microangiopathy in first degree relatives; a case report

open access: yesBMC Nephrology, 2012
Background Anti-glomerular basement membrane glomerulonephritis and thrombotic microangiopathy are rare diseases with no known coherence. Case Presentation A daughter and her biological mother were diagnosed with pregnancy-induced thrombotic ...
Idorn Thomas   +7 more
doaj   +1 more source

Distinct Complement Activation Profiles Between NELL1‐ and PLA2R‐Associated Membranous Nephropathy: A Clinicopathological and Proteomic Study

open access: yesNephrology, Volume 31, Issue 10, October 2026.
We compared the clinicopathological features and complement activation profiles of PLA2R‐associated and NELL1‐associated membranous nephropathy. NELL1‐associated membranous nephropathy was associated with older age, more chronic histologic changes and less glomerular C3 and C4d deposition.
Taihei Suzuki   +12 more
wiley   +1 more source

Angiopoietin correlates with glomerular capillary loss in anti-glomerular basement membrane glomerulonephritis [PDF]

open access: yes, 2002
Angiopoietin correlates with glomerular capillary loss in anti-glomerular basement membrane glomerulonephritis.BackgroundEmerging evidence suggests that endothelial turnover occurs in several glomerular diseases and correlates with resolution or ...
Li, Xiao Zhong   +4 more
core   +1 more source

Increase in podocyte number induced by SV40T antigen during the fetal stage does not expand glomerular size in mice

open access: yesPhysiological Reports, Volume 14, Issue 19, October 2026.
Introduction of SV40 large T antigen (SV40T) in embryonic mouse podocytes via a Tet‐On system markedly increased podocyte number at birth (P0). However, the supernumerary podocytes formed multilayers and detached into the urinary space, failing to enlarge the glomerular tuft area.
Taiji Matsusaka   +3 more
wiley   +1 more source

Diagnostic and management challenges in Goodpasture's (anti-glomerular basement membrane) disease [PDF]

open access: yes, 2018
Goodpasture’s or anti-glomerular basement membrane (GBM) disease is classically characterized by the presence of circulating autoantibodies directed against the non-collagenous domain of the α3 chain of type IV collagen, targeting glomerular and alveolar
Salama, A, Henderson, S
core  

Rapidly progressive glomerulonephritis due to anti-glomerular basement membrane disease accompanied by IgA nephropathy: a case report

open access: yes, 2014
Anti-glomerular basement membrane (anti-GBM) disease is characterized by autoantibodies against antigenic site on type IV collagen of the GBM. The coexistence of anti-GBM disease and other immune complex mediated glomerulonephritis is common.
Xia, Wenli   +4 more
core   +1 more source

Sarsasapogenin Preserves Podocyte Integrity and Attenuates Renal Injury in Experimental IgA Nephropathy

open access: yesThe FASEB Journal, Volume 40, Issue 17, 15 September 2026.
Experimental IgA nephropathy leads to renal inflammation, fibrosis, podocyte injury, and impaired renal function. Sarsasapogenin treatment attenuated inflammatory and profibrotic signaling, reduced extracellular matrix accumulation, preserved nephrin and podocin expression, improved podocyte ultrastructure, and ameliorated renal histopathological ...
Meltem Kumaş   +7 more
wiley   +1 more source

Anti-glomerular Basement Membrane Disease with Antiphospholipid Syndrome [PDF]

open access: yes
A 48-year-old woman presented with a fever, microscopic hematuria, proteinuria, and rapid deterioration of the renal function. Pulmonary alveolar hemorrhaging and a high level of anti-glomerular basement membrane (GBM) antibodies (700 IU/mL) were ...
Torigoe, Miki   +5 more
core  

Efficacy and Safety of Rituximab in Antiglomerular Basement Membrane Disease

open access: yesKidney International Reports
Introduction: Anti–glomerular basement membrane (GBM) disease is caused by pathogenic antibodies usually targeting the noncollagenous domain of the α3 chain of type IV collagen and frequently presents as rapidly progressive glomerulonephritis and diffuse
Vanja Ivković   +15 more
doaj   +1 more source

Home - About - Disclaimer - Privacy