Results 181 to 190 of about 21,129 (222)

Correction: Pulmonary arteritis in the course of granulomatosis with polyangiitis. [PDF]

open access: yesRheumatol Int
Sobuń A   +5 more
europepmc   +1 more source

Concordance between presenting features and relapse in granulomatosis with polyangiitis: implications for risk assessment and counselling. [PDF]

open access: yesRMD Open
Iudici M   +24 more
europepmc   +1 more source

Eosinophilic granulomatosis with polyangiitis

Medicina Clínica (English Edition), 2023
Eosinophilic 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, 2023
A 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
  +4 more sources

Granulomatosis with Polyangiitis (Wegener’s Granulomatosis)

2014
Granulomatosis 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
  +5 more sources

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