Results 11 to 20 of about 6,619,911 (229)

Plasmapheresis, immunosuppressive therapy and anti-GBM disease prognosis: a cohort study of 107 patients [PDF]

open access: yesRenal Failure
Background Anti-glomerular basement membrane (anti-GBM) disease presents with rapidly progressive glomerulonephritis and alveolar hemorrhage, requiring urgent management.
Ying Liu   +11 more
doaj   +5 more sources

Anti-GBM Disease in Pregnancy [PDF]

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2015
Antiglomerular basement membrane (GBM) disease presenting during pregnancy is uncommon. We present a case of a pregnant female who presented with acute renal failure requiring dialysis due to anti-GBM disease.
Mohammed Muqeet Adnan MD   +5 more
doaj   +3 more sources

A case of aggressive atypical anti-GBM disease complicated by CMV pneumonitis [PDF]

open access: yesBMC Nephrology, 2019
Background Anti-glomerular basement membrane (anti-GBM) disease is characterized by circulating IgG glomerular basement membrane antibodies and is clinically expressed as a rapidly progressive crescentic glomerulonephritis (GN), with 30–60% of patients ...
Barbora Sporinova   +6 more
doaj   +3 more sources

Relationship Between Serum Complement C3 Levels and Outcomes Among Patients With Anti-GBM Disease [PDF]

open access: yesFrontiers in Immunology, 2022
BackgroundIgG and complement 3 (C3) are generally found to be deposited along the glomerular basement membrane (GBM) in human anti-GBM disease. The pathogenic role of complement activation in kidney damage of anti-GBM disease has been explored in recent ...
Mengyue Zhu   +6 more
doaj   +4 more sources

Clinical features and prognosis of patients with anti-GBM disease combined with mesangial IgA deposition [PDF]

open access: yesFrontiers in Immunology
IntroductionAnti-GBM diseases with IgA deposition in the mesangial region are rarely described.The factors influencing renal prognosis in patients with anti-GBM disease combined with mesangial IgA deposition are unknown.MethodsWe searched the ...
Wei Ning   +11 more
doaj   +4 more sources

Sequential development of ANCA‐associated vasculitis and anti‐GBM disease: A report of two cases [PDF]

open access: yesClinical Case Reports (discontinued), 2021
In case of AAV with kidney involvement, physicians should explore anti‐GBM antibodies and be aware of the possible sequential development of AAV, especially with MPO‐ANCA, and anti‐GBM glomerulonephritis.
Camille le Moine
exaly   +3 more sources

Veno-venous extracorporeal membrane oxygenation (VV-ECMO) for life-threatening isolated pulmonary anti-GBM disease [PDF]

open access: yesRespiratory Medicine Case Reports, 2022
Anti-glomerular basement membrane disease (anti-GBM disease) associated with renal and lung lesions has a poor prognosis. Diffuse alveolar hemorrhage (DAH) is a complication that worsens anti-GBM disease prognosis.
Shogo Goda   +2 more
doaj   +2 more sources

Immunological overlap stratification in anti-GBM disease: prognostic differences and serological correlations—a single-center retrospective cohort study [PDF]

open access: yesFrontiers in Immunology
BackgroundAnti-glomerular basement membrane (anti-GBM) disease is not a distinct, isolated entity but rather a condition that frequently overlaps with other autoimmune serological profiles.
Yujun Qian   +9 more
doaj   +2 more sources

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   +2 more sources

When Atypical Becomes Typical: A Fulminant Seronegative Anti-GBM Disease [PDF]

open access: yesKidney Medicine
Anti-glomerular basement membrane (GBM) disease is a rare autoimmune disorder characterized by circulating anti-GBM antibodies, rapidly progressive glomerulonephritis, and linear immunoglobulin G (IgG) deposition along the GBM. In contrast, atypical anti-
Faten Y. Andrawes-Barbara   +4 more
doaj   +2 more sources

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