Results 31 to 40 of about 74,969 (210)

SARS-CoV-2 infection and recurrence of anti-glomerular basement disease: a case report

open access: yesBMC Nephrology, 2021
Background Anti-glomerular basement membrane disease (GBM) disease is a rare autoimmune disease causing rapidly progressive glomerulonephritis and pulmonary haemorrhage.
Alexander Winkler   +5 more
doaj   +1 more source

IgA mediated anti-glomerular basement membrane disease with associated circulating anti-neutrophil cytoplasm antibodies [PDF]

open access: yesJournal of Nephropathology
Anti-glomerular basement membrane (anti-GBM) disease is an aggressive small vessel vasculitis usually mediated by IgG autoantibodies. We describe the case of a 73-year-old male with rapidly progressive renal failure that was diagnosed with IgA mediated ...
Patricia Alves   +4 more
doaj   +1 more source

Long-term outcome of anti-glomerular basement membrane antibody disease treated with immunoadsorption. [PDF]

open access: yesPLoS ONE, 2014
Anti-glomerular basement membrane (GBM) antibody disease may lead to acute crescentic glomerulonephritis with poor renal prognosis. Current therapy favours plasma exchange (PE) for removal of pathogenic antibodies.
Peter Biesenbach   +8 more
doaj   +1 more source

Atypical Antiglomerular Basement Membrane Disease in a Pregnant Patient with Systemic Lupus Erythematosus

open access: yesCase Reports in Nephrology, 2023
Antiglomerular basement membrane disease (anti-GBM) is an unusual cause of glomerulonephritis. Patients usually present with rapidly progressive glomerulonephritis with or without pulmonary hemorrhage.
Areerat Ounhasuttiyanon   +2 more
doaj   +1 more source

Clinicopathological characteristics and predictors of poor outcome in anti-glomerular basement membrane disease – a fifteen year single center experience

open access: yesRenal Failure, 2021
Introduction Anti-glomerular basement membrane (anti-GBM) disease is a small vessel vasculitis affecting the renal and lung capillary beds. We aim to study the clinicopathological characteristics and predictors of poor outcome of this disease in our ...
Zafirah Zahir   +3 more
doaj   +1 more source

Tolerance and Autoimmunity in Anti-GBM Disease [PDF]

open access: yesJournal of the American Society of Nephrology, 2003
Anti-glomerular basement membrane (GBM) or Goodpasture’s disease is an uncommon cause of acute renal failure, with an incidence of only 0.5–1 cases/million per year, making it an unfamiliar clinical entity to many physicians.
Alan D. Salama, Jeremy B. Levy
openaire   +1 more source

The Immunobiological Agents for Treatment of Antiglomerular Basement Membrane Disease

open access: yesMedicina, 2023
Combination therapy with glucocorticoids, cyclophosphamide, and plasmapheresis is recommended as the standard treatment for anti-glomerular basement membrane (anti-GBM) disease, but the prognosis of this disease remains poor.
Marina Yamashita   +3 more
doaj   +1 more source

Goodpasture’s Syndrome with Negative Anti-glomerular Basement Membrane Antibodies

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2017
A young male patient with rapidly progressive and life-threatening pulmonary haemorrhage due to anti-glomerular basement membrane (anti-GBM) antibody disease without renal involvement repeatedly tested negative for serum anti-GBM antibodies.
Tjitske Berends-De Vries   +5 more
doaj   +1 more source

The clinical and immunological features of the post-extracorporeal shock wave lithotripsy anti-glomerular basement membrane disease

open access: yesRenal Failure, 2021
Introduction Extracorporeal shock wave lithotripsy (ESWL) is a noninvasive modality to treat urolithiasis, with complications including tissue damage and hematoma of kidney parenchyma.
Beining Wang   +4 more
doaj   +1 more source

A Case of Simultaneous, Biopsy-Proven, Classic, ANCA-Positive Wegener's Granulomatosis and Anti-GBM Disease, but without Detectible Circulating Anti-GBM Antibodies

open access: yesThe Scientific World Journal, 2010
Wegener's granulomatosis (WG) is a systemic, necrotizing, granulomatous vasculitis of unknown etiology. Approximately 75% of cases present as classic WG with both pulmonary and renal involvement, while the remaining 25% of patients present with a limited
Aleksandra Gmurczyk   +5 more
doaj   +1 more source

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