Results 31 to 40 of about 17,551 (206)
Anti-neutrophil cytoplasmic antibodies in new-onset systemic lupus erythematosus [PDF]
: Background: The clinical significance of anti-neutrophil cytoplasmic antibodies in patients with new-onset systemic lupus erythematosus, especially in systemic disease accompanied by interstitial lung disease remains to be elucidated.
Fang Su +5 more
doaj +1 more source
Proteinase 3 (PR3)-Antineutrophil Cytoplasmic Antibody in a Patient with Minimal Change Disease: An Unusual Finding [PDF]
Antineutrophil cytoplasmic antibodies (ANCA) are useful as markers for systemic vasculitis. PR3-ANCA antibodies have been also identified in association with chronic inflammatory and infectious conditions, other autoimmune diseases, malignancy, and ...
Joana Freitas +6 more
doaj +1 more source
Do we need broad immunological work-up in all patients with CIS? [PDF]
BACKGROUND: The aim of this study was to determine the prevalence of altered immunological tests and their clinical significance in patients with clinically isolated syndrome (CIS) suggestive of multiple sclerosis (MS). ----- PATIENTS AND METHODS:
Adamec, Ivan +6 more
core +1 more source
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disorder (MOGAD) is a newly identified autoimmune demyelinating disorder that is often associated with acute disseminated encephalomyelitis and usually occurs postinfection or postvaccination.
Yuki Matsumoto +10 more
doaj +1 more source
Propylthiouracil-induced cutaneous vasculitis [PDF]
The use of propylthiouracil (PTU) is associated with the development of different auto-antibodies, amongst them are antineutrophil cytoplasmic antibodies (ANCA) that are involved in the pathogenesis of ANCA associated systemic vasculitis.
Costa, Leonardo Atem Gonçalves A. +4 more
core +2 more sources
Pachymeningitis is a progressive disease resulting in a diffuse thickening of dura mater due to inflammation, tumor or autoimmune diseases, but most cases are idiopathic.
S. El Aoud +5 more
doaj +1 more source
Is serum HMGB1 a biomarker in ANCA-associated vasculitis? [PDF]
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are systemic inflammatory disorders that include granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), Churg-Strauss syndrome and renal limited ...
Bijl, Marc +6 more
core +3 more sources
Asbestos and Probable Microscopic Polyangiitis
Several inorganic dust lung diseases (pneumoconioses) are associated with autoimmune diseases. Although autoimmune serological abnormalities are common in asbestosis, clinical autoimmune/collagen vascular diseases are not commonly reported.
George S Rashed Philteos +4 more
doaj +1 more source
Associação de doença do anticorpo anti-membrana basal glomerular com dermatomiosite e psoríase: relato de caso [PDF]
CONTEXT: Anti-glomerular basement membrane (anti-GBM) antibody syndrome is characterized by deposition of anti-GBM antibodies on affected tissues, associated with glomerulonephritis and/or pulmonary involvement.
Buosi, Ana Letícia Pirozzi +5 more
core +2 more sources
Antineutrophil cytoplasmic antibodies in Wegener's granulomatosis [PDF]
The prevalence of antineutrophil cytoplasmic antibodies (ANCA) was studied in 12 children with Wegener's granulomatosis. The serum samples were taken in the active phase of disease and were screened for ANCA by indirect immunofluorescence with normal neutrophils and enzyme linked immunosorbent assay (ELISA) using crude neutrophil extract, proteinase 3,
S N, Wong, V, Shah, M J, Dillon
openaire +2 more sources

