Results 61 to 70 of about 11,205 (172)

Study of glomerulonephritis evolution in Castilla-La Mancha (GLOMANCHA) between 1994 and 2008

open access: yesNefrología (English Edition), 2016
Background: Renal biopsy registries allow histopathological data to be collected to improve knowledge of different pathologies and their natural history.
José Luis Conde Olasagasti   +10 more
doaj   +1 more source

DNASE1L3 Deficiency With Novel Missense Variant: Enzymatic and Plasma Fragmentomic Evidence of Pathogenicity and Partial Response to JAK Blockade

open access: yesACR Open Rheumatology, Volume 8, Issue 2, February 2026.
Objective Biallelic loss‐of‐function variants in DNASE1L3 cause inherited systemic lupus erythematosus and hypocomplementemic urticarial vasculitis. These disorders arise from defective clearance of extracellular chromatin, leading to autoantibody formation, immune complex deposition, and complement consumption.
Annel Andrea Leon Tenorio   +369 more
wiley   +1 more source

Membranoproliferative glomerulonephritis with syphilis involvement and possible Hepatitis B virus contribution: a case report

open access: yesBMC Nephrology
Background Syphilis, a sexually transmitted disease, presents with a wide range of clinical manifestations. As the global rate of syphilis infection continues to rise, so does the incidence of syphilis-associated nephritis.
Yan Pan   +5 more
doaj   +1 more source

Comparative analysis of renal decline rates in microscopic polyangiitis: unveiling the slowly progressive phenotype

open access: yesImmunological Medicine
Although rapidly progressive glomerulonephritis (RPGN) is the main renal phenotype of microscopic polyangiitis (MPA), we aim to clarify the clinical features of slowly progressive MPA. This retrospective observational study included 12 patients diagnosed
Kanako Tsutsumi   +8 more
doaj   +1 more source

Microscopic polyangiitis: An unusual neurologic complication

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2011
Microscopic polyangiitis is a systemic necrotizing vasculitis of the small vessels. Its typical clinical manifestations are rapidly progressive glomerulonephritis and alveolar hemorrhage.
Hayet Kaaroud   +8 more
doaj  

Development of anti-glomerular basement membrane glomerulonephritis during the course of IgA nephropathy: a case report

open access: yesBMC Nephrology, 2019
Background Anti-glomerular basement membrane (GBM) glomerulonephritis does not usually coexist with another glomerulonephritis such as IgA nephropathy.
Tadasu Kojima   +8 more
doaj   +1 more source

Membranous nephropathy followed by anti-glomerular basement disease: A case report and review of clinical presentation and treatment

open access: yesSAGE Open Medical Case Reports, 2018
Membranous nephropathy is a common cause of nephrotic syndrome in adults and can be primary or secondary through autoimmune disease, medication, infection, or malignancy.
Claudius Speer   +5 more
doaj   +1 more source

ANCA-Positive Pauci-Immune rapidly progressive glomerulonephritis and the nephrotic syndrome

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2010
We herewith report a case of biopsy proven crescentic glomerulonephritis (GN) due to vasculitis, whose sole presentation was the nephrotic syndrome. Our case raises the possibility of whether the disease initially was a primary GN, upon which crescentic ...
Jabur Wael, Saeed Hareth
doaj  

Rapidly Progressive Glomerulonephritis

open access: yes, 2011
Rapidly Progressive Glomerulonephritis are a group of renal diseases which are still posing serious threat to human health and survival. They are all characterised by acute and rapid deterioration of renal function. Renal biopsy reveals extracapillary glomerulonephritis, most frequently circumferential and diffuse, and immunofluorescence findings ...
openaire   +3 more sources

[Rapidly progressing glomerulonephritis].

open access: yesTidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1992
20 patients with rapidly progressive glomerulonephritis were treated at the nephrological section, Medical Department A, Haukeland Hospital from 1973 to 1988. Nine patients had an idiopathic type of nephritis, while seven patients had this type of glomerulonephritis secondary to systemic lupus erythematosus, endocapillary glomerulonephritis, Henoch ...
B M, Iversen   +3 more
openaire   +1 more source

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