Results 181 to 190 of about 21,129 (222)
Correction: Pulmonary arteritis in the course of granulomatosis with polyangiitis. [PDF]
Sobuń A +5 more
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Concordance between presenting features and relapse in granulomatosis with polyangiitis: implications for risk assessment and counselling. [PDF]
Iudici M +24 more
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Effectiveness of low-dose mepolizumab in refractory eosinophilic granulomatosis with polyangiitis: systemic steroid use and remission. [PDF]
Kim MA +6 more
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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 ...
Yann Nguyen, Loïc Guillevin
openaire +3 more sources
Granulomatosis with polyangiitis
Journal of Clinical Images and Medical Case Reports, 2023A 30 year old male presented to the emergency department with a 6 month history of hemoptysis and epistaxis. He was otherwise healthy with no known medical conditions, no prior surgery, and was taking no medications. His vital signs were normal and his oxygen saturation was 99% SaO2 on room air.
Dilek Karadoğan +2 more
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Granulomatosis with Polyangiitis (Wegener’s Granulomatosis)
2014Granulomatosis with polyangiitis (formerly, Wegener’s granulomatosis) is a systemic necrotizing and granulomatous vasculitis predominantly affecting small-sized vessels. It is also one of the three vasculitides associated with anti-neutrophil cytoplasm antibodies (ANCA).
Susanne Schinke +2 more
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