Results 11 to 20 of about 75,613 (208)
Standardisation of PR3-ANCA and MPO-ANCA: evaluation of certified reference materials [PDF]
Annals of the Rheumatic Diseases, 2020 Antineutrophil cytoplasmic antibodies (ANCAs) are important laboratory markers to support the diagnosis of ANCA-associated vasculitis. A 2017 international consensus states that high-quality immunoassays for proteinase-3 (PR3)-ANCA and myeloperoxidase (MPO)-ANCA can be used as the primary screening method for patients suspected of having granulomatosis
Xavier Bossuyt +8 more
openaire +3 more sources
Microscopic polyangiitis: Modern concepts and treatment options
Научно-практическая ревматология, 2021 The article summarizes the modern concepts of microscopic polyangiitis (MPA), a primary ANCA-associated systemic necrotizing vasculitis without immune globulin deposition (pauci-immune) that affects mainly small vessels, while granulomatous inflammation ...
I. T. Murkamilov +6 more
doaj +1 more source
Supplementary Material for: Multi-organ Relapse Following COVID-19 in MPO-ANCA-Associated Vasculitis: A Case Report [PDF]
, 2023 Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a complex systemic autoimmune disease characterized by small vessel vasculitis. Typically, the relapse rate is lower in patients with end-stage kidney disease (ESKD) than in those
Choi S.R. (17232316) +6 more
core +1 more source
Медицинская иммунология, 2020 Eosinophilic granulomatosis with polyangiitis (EGPA), previously called Churg—Strauss syndrome, represents a rare form of ANCA-associated necrotising vasculitis which affects small vessels.
V. N. Marchenko +7 more
doaj +1 more source
Pauci-immune ANCA associated glomerulonephritis. Clinical case [PDF]
, 2023 The female patient with extracapillary pauci-immune AncA associated glomerulonephritis having antibodies against myeloperoxidase and dialysis-requiring renal failure is described.
Rosa M. Vakolyuk +6 more
core +1 more source
Journal of Family Medicine and Primary Care, 2020 Granulomatous polyangiitis (GPA) is a small vessel vasculitis commonly affecting the upper and lower respiratory tracts and kidneys. About 90% of the cases are associated with ANCA, namely, PR3-ANCA and MPO-ANCA.
Iadarilang Tiewsoh +5 more
doaj +1 more source
ANCA associated vasculitis subtypes: Response (response to letter) [PDF]
, 2022 Many thanks for the opportunity to respond to the interesting letter to the Editor from Merkel, Jayne, and Bekker, with regard to our publication “ANCA Associated Vasculitis Subtypes: Recent Insights and Future Perspectives”.1In the management section of
Robson, Joanna C +6 more
core +2 more sources
A Case of Granulomatosis With Polyangiitis Mimicking Chronic Sinusitis With Polyp [PDF]
Journal of RhinologyA diagnosis of granulomatosis with polyangiitis (GPA) can be challenging due to its diverse and nonspecific clinical manifestations, and it is often misdiagnosed as a simple inflammatory disease.
Minji Oh, Sung Jae Heo
doaj +1 more source
Cumulative MPA incidence in MPO-ANCA-positive and -negative IIP patients. [PDF]
, 2018 The 5-year MPA incidence was 24.3% in the MPO-ANCA-positive IIP patients and 0% in the MPO-ANCA-negative IIP patients. P
Noriyuki Enomoto (322372) +11 more
core +1 more source
Medicina, 2020 Background and objectives: Goodpasture’s syndrome (GS) is a rare, life-threatening autoimmune disease. Although the coexistence of anti-neutrophil cytoplasmic antibody (ANCA) with Goodpasture’s syndrome has been recognized, the impacts of ...
Charat Thongprayoon +11 more
doaj +1 more source