Disease | wegener granulomatosis |
Phenotype | C0042384|vasculitis |
Sentences | 8 |
PubMedID- 22247758 | Evidence is lacking for direct pathogenicity of human anti-proteinase-3 (pr3) antibodies in development of systemic vasculitis and granulomatosis with polyangiitis (gpa, wegener's granulomatosis). |
PubMedID- 25390916 | Purpose: the purpose of this study was to report the use of plasmapheresis in the management of choroidal vasculitis associated with wegener granulomatosis. |
PubMedID- 23480833 | Expert opinion: small-vessel anti-neutrophil cytoplasmic antibody (anca)-associated vasculitis, especially granulomatosis with polyangiitis (wegener's granulomatosis) are the most frequent causes of pulmonary vasculitis and typically present as nodules, alveolar infiltrates (haemorrhagic or not), cavities or tracheobronchial stenosis. |
PubMedID- 20695860 | Granulomatous vasculitis is classically associated with wegener's granulomatosis, lymphomatoid granulomatosis or churg-strauss syndrome. |
PubMedID- 25332635 | vasculitis like granulomatosis with polyangitis (wegener's granulomatosis), churg strauss syndrome and sarcoidosis, which are the second consideration, are ruled out by serological investigations. |
PubMedID- 21147630 | According to the american college of rheumatology (acr), classification criteria of the css are: small vessel vasculitis along with wegener's granulomatosis (wg), microscopic polyangiitis (mpa), and idiopathic necrotizing crescentic glomerulonephritis ncgn [3]. |
PubMedID- 25859349 | Anti-neutrophil cytoplasmic antibody (anca)-associated vasculitis includes granulomatosis with polyangiitis (wegener's granulomatosis) and microscopic polyangiitis. |
PubMedID- 21876314 | He was diagnosed with antineutrophil cytoplasmic antibody-associated vasculitis due to wegener granulomatosis, microscopic polyangiitis, or drug induction. |
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