Identification of novel clinical subtypes in patients with microscopic polyangiitis using cluster analysis: multicenter REVEAL cohort study. [PDF]
Okazaki A +12 more
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Poor prognostic factors for relapse of interstitial lung disease in microscopic polyangiitis: the Japanese multicentre REVEAL cohort study. [PDF]
Matsuda S +14 more
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Prognosis of microscopic polyangiitis is well predictable in the first 2 weeks of treatment. [PDF]
Owaki A +6 more
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Clinical features, radiological findings and prognosis of microscopic polyangiitis with interstitial lung disease: a retrospective matched control study. [PDF]
Song Q +5 more
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Serum Soluble Receptors for Advanced Glycation End-Products May Predict Mortality in Microscopic Polyangiitis and Granulomatosis with Polyangiitis. [PDF]
Yoon T +6 more
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Microscopic polyangiitis in pediatric systemic lupus erythematosus: a unique presentation of pulmonary-renal syndrome and case report of an overlap syndrome. [PDF]
Zhang CX +4 more
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Remission induction therapies and long-term outcomes in granulomatosis with polyangiitis and microscopic polyangiitis: real-world data from a European cohort. [PDF]
Krämer S +8 more
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Microscopic polyangiitis is a systemic vasculitis affecting smal-l and medium-sized vessels and is characteristically associated with a focal and segmental necrotizing glomerulonephritis. It may present as a pulmonary-renal syndrome with rapidly progressive glomerulonephritis and alveolar hemorrhage, but the pattern of disease will vary according to ...
Lucy, Smyth +2 more
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Microscopic polyangiitis was initially considered a "microscopic" form of polyarteritis nodosa and was not definitively distinguished from it until the Chapel Hill nomenclature (1994). Microscopic polyangiitis is a systemic necrotizing vasculitis of small vessels.
Christian, Pagnoux +2 more
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Microscopic polyangiitis (MPA) is a pauci-immune necrotizing small vessel vasculitis in which necrotizing crescentic glomerulonephritis (GN) is very common and pulmonary capillaritis often occurs. It belongs to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis and can be differentiated from granulomatosis with polyangiitis (
SINICO, RENATO ALBERTO +4 more
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