Results 171 to 180 of about 626,430 (205)
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Sialadenitis in Antineutrophil Cytoplasmic Antibodies Vasculitis

Journal of The Association of Physicians of India
Granulomatosis 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
openaire   +2 more sources

Sputum Antineutrophil Cytoplasmic Antibodies in Serum Antineutrophil Cytoplasmic Antibody–Negative Eosinophilic Granulomatosis with Polyangiitis

American Journal of Respiratory and Critical Care Medicine, 2019
Abstract Rationale 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.
Manali, Mukherjee   +13 more
openaire   +2 more sources

Antineutrophil cytoplasmic antibody-associated vasculitis

Current Opinion in Nephrology & Hypertension
Purpose of review This review focuses on latest developments in managing antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV), a systemic autoimmune condition characterized by inflammation and necrosis of small blood vessels due to circulating autoantibodies that target neutrophilic granules.
Raghunandan, Konda   +2 more
openaire   +2 more sources

Update on antineutrophil cytoplasmic antibody vasculitis

Current Opinion in Nephrology & Hypertension
Purpose of review The purpose of this review is to discuss antineutrophil cytoplasmic antibody (ANCA) vasculitis (microscopic polyangiitis and granulomatosis with polyangiitis) and how we have arrived at our current guidelines and treatment methods.
Dan A, Mandel   +3 more
openaire   +2 more sources

Antineutrophil cytoplasmic antibody-associated vasculitides

Joint Bone Spine, 2007
The identification of antineutrophil cytoplasmic antibodies (ANCA) proved a major breakthrough in the classification, diagnosis, monitoring, and understanding of vasculitides. Vasculitides associated with ANCA selectively affect the small vessels; they include Wegener granulomatosis, microscopic polyangiitis, and Churg-Strauss syndrome.
openaire   +2 more sources

Antineutrophil Cytoplasmic Antibody and the Gastroenterologist

Journal of the Royal Society of Medicine, 1992
W, Dickey, S, McMillan
openaire   +2 more sources

Antineutrophil Cytoplasmic Antibodies and Organ-Specific Manifestations in Eosinophilic Granulomatosis with Polyangiitis: A Systematic Review and Meta-Analysis

Journal of Allergy and Clinical Immunology: in Practice, 2021
Hsiou-Hsin Tsai   +2 more
exaly  

Are antineutrophil cytoplasmic antibodies pathogenic? Experimental approaches to understand the antineutrophil cytoplasmic antibody phenomenon.

Rheumatic diseases clinics of North America, 2002
Antineutrophil cytoplasmic antibodies (ANCA) directed against the neutrophil enzymes PR3 and MPO are tightly associated with the development of small vessel vasculitis. This article reviews the large body of data derived from in vitro experiments documenting many different proinflammatory effects of these ANCA on neutrophils, monocytes, and endothelial
K A, Russell, U, Specks
openaire   +1 more source

ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES

The Lancet, 1989
R.A Thompson, S.S Lee
openaire   +1 more source

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