Immunological Markers Associated with Skin Manifestations of EGPA
Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare systemic vasculitis with eosinophilic inflammation and variable clinical presentations. Although skin manifestations are frequent, current classification criteria do not include them, which
Brunetto, Silvia +7 more
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Heart Failure with Recovered Ejection Fraction: EGPA-Associated Cardiomyopathy Treated with Benralizumab. [PDF]
Bangari LR +9 more
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Early recognition of eosinophilic granulomatosis with polyangiitis in outpatient settings: musculoskeletal and gastrointestinal clues beyond respiratory disease. [PDF]
Aitella E, De Martinis M, Ginaldi L.
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Carlo Mümmler,1 Pontus Mertsch,1 Michaela Barnikel,1 Frank Haubner,2 Ulf Schönermarck,3 Ulrich Grabmaier,4 Hendrik Schulze-Koops,5 Jürgen Behr,1 Nikolaus Kneidinger,1,6 Katrin Milger1 1Department of Medicine V, LMU University Hospital, LMU Munich ...
Mümmler C +9 more
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Mitral and tricuspid valve repair in a patient with eosinophilic granulomatosis with polyangiitis. [PDF]
Dąbrowska A +3 more
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Eosinophilic granulomatosis with polyangiitis (EGPA) is an eosinophilic vasculitis frequently involving both upper and lower airways, commonly associated with severe asthma and chronic rhinosinusitis with nasal polyps (CRSwNP).
Lazzeroni, Matteo +13 more
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An Evolving Clinical Phenotype Preceding the Diagnosis of Eosinophilic Granulomatosis With Polyangiitis: A Case Report. [PDF]
Knowles M, Leung PHT, Chandran S.
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Healthcare resource utilisation and associated costs in patients with eosinophilic granulomatosis with polyangiitis in England: A retrospective observational cohort study. [PDF]
Siddiqui SH +12 more
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Eosinophilic Granulomatosis With Polyangiitis Presenting With Rare Neurological Manifestations. [PDF]
Bruneau VG, Lavigne AM.
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Early mepolizumab initiation during remission induction is associated with lower organ damage burden in EGPA: a multicentre cohort study. [PDF]
Maruyama A +12 more
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