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Correction to "A Randomized, Double-Blind, Placebo-Controlled Trial of Abatacept for the Treatment of Relapsing, Nonsevere Granulomatosis With Polyangiitis". [PDF]
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Diagnosis and classification of granulomatosis with polyangiitis (aka Wegener's granulomatosis)
Granulomatosis with polyangiitis (GPA, formerly known as Wegener's Granulomatosis) is an autoimmune small vessel vasculitis which is highly associated with anti-neutrophil cytoplasmic antibodies (ANCA).
David D'Cruz
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Eosinophilic granulomatosis with polyangiitis
Medicina Clínica (English Edition), 2023Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterized by the presence of asthma associated with eosinophilia, eosinophilic infiltration of different organs, and vasculitis of small and medium-sized vessels. Although classified as anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, it occurs in less ...
Carlos, Romero Gómez +2 more
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Granulomatosis with Polyangiitis in Childhood
Current Rheumatology Reports, 2012Granulomatosis with polyangiitis (GPA) is a rare yet frequently organ- or life-threatening systemic vasculitis affecting small- to medium-sized arteries in multiple organs. It characteristically leads to alveolar hemorrhage and destructive, pauci-immune glomerulonephritis. GPA is also characterized by granulomas in the upper and lower respiratory tract
Marinka, Twilt +2 more
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Granulomatosis with polyangiitis (Wegener's)
Joint Bone Spine, 2020Granulomatosis with polyangiitis (GPA) (Wegener) is a necrotizing vasculitis combining inflammation of the vascular wall and peri- and extravascular granulomatosis. Clinically, GPA is characterized in its full form by ENT signs, lung, and kidney involvement.
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Granulomatosis with polyangiitis
Oral Surgery, 2014AbstractGranulomatosis with polyangiitis (GPA), which was formerly known as Wegener's granulomatosis, is a rare systemic condition with oral manifestations. This case report describes and discusses the oral presentation, investigations, diagnosis and management options in a patient who was diagnosed with GPA.
P. Hoyle, J.C. Steele
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Eosinophilic Granulomatosis With Polyangiitis
JAMA Dermatology, 2021Abraham M, Korman, Catherine G, Chung
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