Results 41 to 50 of about 2,533,954 (307)
Clinical Immunology, 2023 Levels of neutrophil extracellular traps (NETs) were measured in plasma of healthy controls (HC, n=30) and patients with granulomatosis with polyangiitis (GPA, n=123), microscopic polyangiitis (MPA, n=61), Takayasu’s arteritis (TAK, n=58), and giant cell
Despina Michailidou +18 more
semanticscholar +1 more source
Significance of autoantibodies in diagnostics of systemic vasculitis [PDF]
Exploration of Musculoskeletal Diseases, 2023 Systemic vasculitis is a heterogeneous group of disorders characterized by inflammation and necrosis in the vessel wall. Patients usually present a quite broad spectrum of manifestations which vary in terms of vessels’ size affected, organs involvement ...
Katarzyna Fischer, Marek Brzosko
doaj +1 more source
Inflammatory bowel disease-specific autoantibodies in HLA-B27-associated spondyloarthropathies: Increased prevalence of ASCA and pANCA [PDF]
, 2004 Aims: An association between inflammatory bowel disease (IBD) and spondyloarthropathies (SpA) has repeatedly been reported. The aim of the present study was to investigate whether serologic markers of IBD, e. g.
Folwaczny, Christian +15 more
core +1 more source
Oman Medical Journal, 2019 Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) is a rare vasculitis in children. It commonly presents with respiratory symptoms, especially asthma, allergic rhinitis, and peripheral eosinophilia.
Wahinuddin Sulaiman +4 more
doaj +1 more source
Kidney International, 1998 Anti-neutrophil cytoplasmic antibodies (ANCA) are widely used as diagnostic markers for Wegener's granulomatosis (WG), microscopic polyangiitis (MPA), Churg-Strauss syndrome (CSS) and idiopathic rapidly progressive glomerulonephritis (iRPGN).
E. Hagen +11 more
semanticscholar +1 more source
Clinical and Experimental Immunology, 2007 Summary In patients with anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, indirect immunofluorescence (IF) distinguishes between cytoplasmic (C-ANCA) and perinuclear (P-ANCA) neutrophil staining patterns.
M. Talor +5 more
semanticscholar +2 more sources
Anti-neutrophil cytoplasmic antibodies in idiopathic inflammatory disorders [PDF]
, 1994 This thesis studies the prevalence of anti-neutrophil cytoplasmic antibodies (ANCA) in idiopathic inflammatory disorders in which GS-ANA were described during the 60s: rheumatoid arthritis, autoimmune liver diseases, inflammatory bowel disease, and ...
Mulder, Alide Heleen Leontine
core +8 more sources
Case for diagnosis. Cutaneous small vessel vasculitis (anti-proteinase 3 positive), fever, hemoptysis, and lung cavitation in an adult, [PDF]
Anais Brasileiros de DermatologiaSmall vessel vasculitis with anti-proteinase antibodies 3 is an atypical clinical presentation of tuberculosis. The authors present the case of a 47-year-old male patient, with palpable purpura and palmoplantar hemorrhagic blisters, with subsequent ...
Luana Moraes Campos +3 more
doaj +2 more sources
A case of Sjögren syndrome and anti-neutrophil cytoplasmic antibody-associated vasculitis
Reumatismo, 2023 Sjögren’s syndrome (SS) is a rare disease with the highest reported prevalence of 0.01-0.09%. Anti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) is another rare auto-immune disease (prevalence of 0.0009-0.01%).
K. Kaynar +3 more
doaj +1 more source
A Challenging Twist in Pulmonary Renal Syndrome
Case Reports in Rheumatology, 2014 Case. We report a rare case of hydralazine-induced anti-neutrophil cytoplasmic antibody-associated vasculitis. A 75-year-old African American woman with history of high blood pressure on hydralazine for 3 years presented with acute onset of shortness of ...
Rajaie Namas +3 more
doaj +1 more source