Results 91 to 100 of about 64,509,941 (193)

Interstitial Lung Disease in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis: A European Multicenter Study

open access: yesArthritis &Rheumatology, Volume 78, Issue 8, Page 1718-1730, August 2026.
Objective Interstitial lung disease (ILD) can occur in association with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV‐ILD) or as an isolated entity with positive ANCA (ANCA‐ILD). However, data on the epidemiology and outcomes of these conditions remain limited.
Aglaia Chalkia   +18 more
wiley   +1 more source

Relationship between serum periostin and disease activity in eosinophilic granulomatosis with polyangiitis.

open access: yes, 2018
Relationship between serum periostin and disease activity in eosinophilic granulomatosis with polyangiitis.
David Cuthbertson (188652)   +16 more
core   +1 more source

Intracerebral hemorrhage after IV tPA for stroke as early symptom of ANCA-associated vasculitis

open access: yeseNeurologicalSci, 2017
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are rare diseases characterized by a necrotizing small-vessel vasculitis and circulating ANCA that comprise granulomatosis with polyangiitis, microscopic polyangiitis, and ...
Neda Zarghami Esfahani   +3 more
doaj   +1 more source

Combination Biologic Therapy with Mepolizumab and Dupilumab for Severe Eosinophilic Granulomatosis with Polyangiitis and Chronic Rhinosinusitis with Nasal Polyp [PDF]

open access: yes
We report the case of a 55-year-old female with eosinophilic granulomatosis with polyangiitis and chronic rhinosinusitis with nasal polyp. Rhinosinusitis recurred 6 months after full-house endoscopic sinus surgery.
Nakamura,Yosuke   +19 more
core   +2 more sources

Mepolizumab For The Treatment Of Patients With Eosinophilic Granulomatosis With Polyangiitis: A Phase Iii Randomized, Placebo-Controlled Trial [PDF]

open access: yes, 2017
Mepolizumab For The Treatment Of Patients With Eosinophilic Granulomatosis With Polyangiitis: A Phase Iii Randomized, Placebo-Controlled ...
Luqmani, R   +37 more
core   +3 more sources

Vasculitis of the upper airways1

open access: yesSwiss Medical Weekly, 2012
Systemic vasculitides are rare and potentially life-threatening diseases. Granulomatosis with polyangiitis (GPA; formerly Wegener’s granulomatosis) and Churg Strauss syndrome (possibly to be renamed eosinophilic granulomatosis with polyangiitis ...
Christian Pagnoux, Nikolaus E Wolter
doaj   +1 more source

Accessory left gastric artery aneurysms in granulomatosis with polyangiitis : a case report and literature review [PDF]

open access: yes, 2017
2017-02Aneurysm formation is a potential complication of granulomatosis with polyangiitis (GPA), previously known as Wegener’s granulomatosis. It is a very rare complication, but immediate diagnosis and therapy should be performed because an aneurysm can
Hayashi, Shogo   +12 more
core   +1 more source

Research progress on the diagnostic value of ANCA in autoimmune diseases of patients with refractory rhinosinusitis

open access: yesImmunobiology
Anti-neutrophil cytoplasmic antibody (ANCA) is an important serological marker for autoimmune diseases, particularly ANCA-associated vasculitis (AAV). AAV frequently presents with refractory rhinosinusitis as an initial manifestation, yet ANCA testing in
Qian Li, Hang Li, Haiyuan Zhao
doaj   +1 more source

Clinical Images: Features of IgG4‐related disease in a patient with granulomatosis with polyangiitis

open access: yes
ACR Open Rheumatology, Volume 8, Issue 8, August 2026.
Florian Kollert   +9 more
wiley   +1 more source

Onset of eosinophilic granulomatosis with polyangiitis in a patient treated with an IL-5 pathway inhibitor for severe asthma

open access: yes, 2020
Onset of eosinophilic granulomatosis with polyangiitis in a patient treated with an IL-5 pathway inhibitor for severe ...
Nalin, Francesca   +4 more
core   +1 more source

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