Results 71 to 80 of about 2,373 (163)
Respirology Case Reports, Volume 14, Issue 2, February 2026.A 67‐year‐old man with cryptogenic organising pneumonia developed recurrent relapses despite corticosteroid and mycophenolate therapy. A complete absence of mannose‐binding lectin was identified, suggesting impaired apoptotic cell clearance as a contributor to persistent inflammation.
Ilias E. Dimeas +4 more
wiley +1 more source
Alu Overexpression Leads to an Increased Double‐Stranded RNA Signature in Dermatomyositis
Arthritis &Rheumatology, Volume 78, Issue 1, Page 209-222, January 2026.Objective Dermatomyositis is an autoimmune condition characterized by a high interferon signature of unknown etiology. Because coding sequences constitute <1.2% of our genomes, there is a need to explore the role of the noncoding genome in disease pathogenesis.
Rayan Najjar +2 more
wiley +1 more source
A rare case of anti-jo1 syndrome presenting as a interstitial lung disease
Journal of Association of Pulmonologist of Tamil Nadu, 2020 Antisynthetase syndrome is a rare entity and can be missed if not specifically looked in patients whose initial presentation is with Interstitial Lung Disease. Prognosis is altered when patients presenting with Interstitial Lung Disease.
A Kirubanandam +3 more
doaj +1 more source
18F-FDG PET/CT IN ANTISYNTHETASE SYNDROME: CASE REPORT
Hematology, Transfusion and Cell TherapyIntroduction/Justification: Antisynthetase syndrome is an autoimmune pathology characterized by production of autoantibodies against aminoacyl tRNA synthetase, mainly anti-Jo-1. Report: Male patient presenting a clinical picture of polyarthritis in hands
Felipe Piccarone Gonçalves Ribeiro +7 more
doaj +1 more source
Skeletal Muscle Involvement in Antisynthetase Syndrome
JAMA Neurology, 2017 Antisynthetase syndrome, characterized by myositis, interstitial lung disease, skin rash, arthropathy, and Raynaud phenomenon, is a clinical entity based on the presence of aminoacyl transfer RNA synthetase (ARS) antibodies in patients' serum. However, antisynthetase syndrome is not included in the histological subsets of idiopathic inflammatory ...
Eri, Noguchi +10 more
openaire +3 more sources
EJ antibody antisynthetase syndrome [PDF]
BMJ Case Reports, 2022 Andrew Robert Benck, Augustine Manadan
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Pericarditis as the Initial Manifestation of Antisynthetase Syndrome: A Case Report
Case Reports in RheumatologyAntisynthetase syndrome is a subtype of idiopathic inflammatory myopathy characterized by clinical manifestations that include myositis with a distinctive muscle biopsy pattern. Cardiac involvement has traditionally been considered a rare feature of this
Gianni Lucchetti, Per Sundbom
doaj +1 more source
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2002 Traditionally, idiopathic inflammatory myopathies have been classified into three groups; polymyositis, dermatomyositis and inclusion body myositis. Recent developments in immunology have improved our knowledge and it is now possible to classify these disorders according to the presence of myositis specific autoantibodies.Four adult patients with anti ...
openaire +1 more source
ANTISYNTHETASE SYNDROME: COURSE OF A RARE DISEASE ON EXAMPLE OF CLINICAL CASE
Journal of V. N. Karazin Kharkiv National University: Series Medicine, 2018 Systemic disorders of connective tissue refer to rare and poorly studied diseases. This group of diseases associated with the variable course and makes it interesting for either medical scientists and researchers or practitioner.
Boateng H. K. +2 more
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