Results 11 to 20 of about 52,218 (248)
Síndrome antissintetase anti-Jo-1 Anti-Jo-1 antisynthetase syndrome [PDF]
Revista Brasileira de Reumatologia, 2010 OBJETIVO: Devido à escassez de estudos populacionais, apresentamos um estudo epidemiológico em síndrome antissintetase anti-Jo-1 (SAS). PACIENTES E MÉTODOS: Estudo coorte retrospectivo realizado em um centro de 1980 a 2010.
Samuel Katsuyuki Shinjo +1 more
doaj +5 more sources
The relevance of anti-Jo-1 autoantibodies in patients with definite dermatomyositis [PDF]
Advances in Rheumatology, 2021 Background To assess the prevalence and clinical relevance of anti-Jo-1 autoantibodies in a representative sample of patients with definite dermatomyositis (DM).
Vanessa Posener de Andrade +3 more
doaj +4 more sources
Anti- Jo-1 myositis with subluxating arthropathy
Indian Journal of Rheumatology, 2022 Asna shaikh +2 more
doaj +2 more sources
Enhanced toxicity to chemoradiation in a patient with Anti-Jo-1-antisynthetase syndrome. [PDF]
BJR Case Rep, 2022 Appropriate counseling of patients with autoimmune connective tissue disorders (ACTDs) is often challenging for radiation oncologists, especially regarding anticipated side-effects of radiation treatment. These patients can have highly variable and unpredictable sequelae from radiation therapy, and the uncertainty builds when radiation is convoluted ...
Valle L +8 more
europepmc +5 more sources
Not every elevating enzyme tells the same story: unpacking creatine kinase and anti-Jo-1 positivity beyond inflammatory myositis [PDF]
Romanian Journal of Rheumatology, 2023 Gitelman syndrome (GS) is an autosomal recessive familial disorder characterized by hypokalemia and metabolic alkalosis. Rhabdomyolysis due to hypokalemia is extremely rare. The presentation of GS leading to rhabdomyolysis is extremely rare as well. This
Dilara Bulut Gökten, Rıdvan Mercan
doaj +1 more source
Antisynthetase Syndrome: A Rare Cause for ILD [PDF]
Journal of Clinical and Diagnostic Research, 2016 Anti-Synthetase Syndrome (ASS) is a rare autoimmune disorder characterized by Interstitial Lung Disease (ILD), inflammatory myositis, fever, Raynaud’s phenomenon, mechanic's hand, and inflammatory polyarthritis in the setting of antibodies against amino
HJ Gayathri Devi +3 more
doaj +1 more source
Autoimmunity, 2005 Anti-Jo-1 antibody is a myositis specific autoantibody most commonly found in patients with idiopathic inflammatory myopathies (IIM). This antibody is directed against the histidyl-tRNA synthetase which catalyses the binding of the histidine to its cognate tRNA during protein synthesis. It can be considered a specific marker of IIM, predominantly found
Sandra, Zampieri +5 more
openaire +4 more sources
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
Common and distinct clinical features in adult patients with anti-aminoacyl-tRNA synthetase antibodies: heterogeneity within the syndrome. [PDF]
PLoS ONE, 2013 OBJECTIVE: To identify similarities and differences in the clinical features of adult Japanese patients with individual anti-aminoacyl-tRNA synthetase antibodies (anti-ARS Abs).
Yasuhito Hamaguchi +14 more
doaj +1 more source
Revista Brasileira de Reumatologia, 2006 Nem sempre é possível estabelecer uma clara distinção entre as doenças musculares de causa infecciosa e as miosites idiopáticas. Há situações, inclusive, em que se considera existir uma relação causal entre ambas as doenças.
Carolina de Souza Müller +3 more
doaj +1 more source