Results 191 to 200 of about 17,550 (209)
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Antineutrophil Cytoplasmic Antibodies in Diffuse Panbronchiolitis
Respiration, 1999<i>Background:</i> There are some reports of the coexistence of chronic suppurative lung diseases such as cystic fibrosis and systemic vasculitis. Diffuse panbronchiolitis has the same characteristics as chronic recurrent sinopulmonary infection and respiratory bronchiolitis.
Y, Sugiyama, S, Kitamura
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Antineutrophil Cytoplasmic Antibodies Testing and Interpretation
Clinics in Laboratory Medicine, 2019The discovery of antineutrophil cytoplasmic antibodies (ANCA) helped establish ANCA-associated vasculitis as a separate and well-defined clinical entity. Its progressive incorporation into the clinical diagnosis algorithms has made ANCA testing a cornerstone immunoassay embedded in the management of ANCA-associated vasculitis.
Hugues, Allard-Chamard, Patrick, Liang
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Clinical value of antineutrophil cytoplasmic antibodies
Current Rheumatology Reports, 2000This article presents a brief review of the clinical value of antineutrophil cytoplasmic antibodies (ANCA) in the diagnosis and management of patients with various forms of vasculitis. ANCA assay methodology and testing recommendations are reviewed. The patterns of reactivity of ANCA observed by indirect immunofluorescence, the antigens recognized by ...
V, Rus, B S, Handwerger
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Antineutrophil Cytoplasmic Antibodies (ANCAs)
Journal of the American Society of NephrologyANCA-associated vasculitis (AAV) is a rare and potentially fatal autoimmune disorder characterized by pauci-immune necrotizing vasculitis affecting small- to medium-sized blood vessels. The pathogenic role of ANCAs in AAV is supported by both clinical and experimental evidence, and when used in the proper clinical setting, ANCA testing is highly ...
Nicole E. Wyatt +3 more
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Sialadenitis in Antineutrophil Cytoplasmic Antibodies Vasculitis
Journal of The Association of Physicians of IndiaGranulomatosis with polyangiitis (GPA) is a pauci-immune vasculitis typically involving upper and lower respiratory tract involvement and crescentic glomerulonephritis. Salivary gland involvement in GPA is rare. When it occurs in GPA, it is commonly seen with sinonasal and lung involvement and rarely with renal involvement.
Aditi, Patankar +3 more
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American Journal of Respiratory and Critical Care Medicine, 2019
Eosinophilic granulomatosis with polyangiitis (eGPA) is a small-vessel vasculitis where 40% of patients present with serum antineutrophil cytoplasmic antibodies (ANCAs). We examined the presence and clinical relevance of sputum ANCAs in the serum ANCA- patients with eGPA.ANCA was investigated in matched sputum and blood samples collected from 23 ...
Manali, Mukherjee +13 more
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Eosinophilic granulomatosis with polyangiitis (eGPA) is a small-vessel vasculitis where 40% of patients present with serum antineutrophil cytoplasmic antibodies (ANCAs). We examined the presence and clinical relevance of sputum ANCAs in the serum ANCA- patients with eGPA.ANCA was investigated in matched sputum and blood samples collected from 23 ...
Manali, Mukherjee +13 more
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[Antineutrophil cytoplasmic antibodies--ANCA].
Casopis lekaru ceskych, 1993Antibodies against cytoplasm of neutrophil leucocytes (ANCA) with a high sensitivity are found in idiopathic necrotizing vasculitis and idiopathic glomerulonephritis with formation of sickles (IGS). C-ANCA are directed against the myeloid lysosomal enzyme--proteinase 3 and are found above all in Wegener's granulomatosis and microscopic polyarteritis. P-
J, Vencovský, A, Palecková, R, Becvár
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[Antineutrophil cytoplasmic antibody(ANCA)].
Rinsho byori. The Japanese journal of clinical pathology, 2003ANCA are associated with small sized vessel vasculitis; one subtype is an antibody against myeloperoxidase(MPO), which stains in a perinuclear pattern(P-ANCA) indirect immunofluorescence(IIF) using a neutrophil substrate, and the other subtype is an antibody against proteinase-3(PR-3), which stains in a diffuse granular cytoplasmic pattern ANCA by IIF.
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