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Granulomatosis with Polyangiitis
2019Granulomatosis with polyangiitis (GPA) is a small-vessel necrotizing vasculitis that most characteristically affects the ear, nose, and throat (ENT), lungs, and/or kidneys. The median age at diagnosis is in the fifth decade, but children and older people can be affected.
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[Granulomatosis with polyangiitis (Wegener's granulomatosis)].
Presse medicale (Paris, France : 1983), 2012Granulomatosis with polyangiitis (GPA), is the recently proposed, new alternative name for Wegener's granulomatosis. It defines a systemic small-vessels vasculitis, characterized by frequent involvement of upper and lower respiratory tract. The presence of cytoplasmic-type ANCA with anti-proteinase 3 specificity is observed in more than 90% of patients
Alexandre, Karras +3 more
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American Journal of Respiratory and Critical Care Medicine, 2020
Mark A. Little, Benjamin Terrier
exaly
Mark A. Little, Benjamin Terrier
exaly
Epidemiology of Granulomatosis With Polyangiitis and Microscopic Polyangiitis in Adults in France
Journal of Autoimmunity, 2022Benjamin Terrier +2 more
exaly
Atypical granulomatosis with polyangiitis
Italian Journal of Dermatology and VenereologyBorriello, Silvia +12 more
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Diagnosis and Classification of Granulomatosis With Polyangiitis (Aka Wegener's Granulomatosis)
Journal of Autoimmunity, 2014David D'Cruz
exaly
Clinic Manifestations in Granulomatosis With Polyangiitis
International Journal of Immunopathology and Pharmacology, 2016Armando De Virgilio +2 more
exaly
Treatment of Granulomatosis With Polyangiitis (Wegener’s)
Expert Review of Clinical Immunology, 2015Loïc Guillevin
exaly