Results 91 to 100 of about 16,326 (177)
Asymptomatic polymyositis with pulmonary disease
We present the case of a medium-aged patient with a alveolo-interstitial pulmonary affection after 5 months of evolution, characterized by cough and progressive dyspnea accompanied by sustained febricula, slight constitutional syndrome and dermatological
Alfonso Déniz, J. +4 more
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IntroductionObservational studies suggest associations between gut microbiota and polymyositis (PM) and dermatomyositis (DM), but causal relationships are unclear.
Yanna Niu +27 more
doaj +1 more source
Ophthalmoplegia associated with polymyositis/dermatomyositis
Polymyositis is an idiopathic inflammatory myopathy that with cutaneous findings is called dermatomyositis.
Mitchell Strominger; Joseph Newman; Kyle Smith
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Pathogenic mechanisms of disease in idiopathic inflammatory myopathies: autoantibodies as clues
Idiopathic inflammatory myopathies (IIMs) encompass a spectrum of autoimmune diseases characterized by muscle inflammation and systemic involvement. This review aimed to synthesize current evidence on the clinical significance and pathogenic mechanisms ...
Yuanhui Wu +8 more
doaj +1 more source
Association between C8orf13–BLK rs13277113 and polymyositis/dermatomyositis.
OR: Odds ratio, CI: confidence interval, PM: polymyositis, DM: dermatomyositis, N.S.: not significant.
Yukiko Hayashi (84287) +7 more
core +1 more source
Elevated risk of venous thromboembolic events in patients with inflammatory myopathies
Michał Nowak, Katarzyna Królak-Nowak, Aleksandra Sobolewska-Włodarczyk, Jakub Fichna, Marcin Włodarczyk Department of Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland Abstract: Venous thromboembolism (
Nowak M +4 more
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Polymyositis and dermatomyositis
The inflammatory myopathies, commonly described as idiopathic, are the largest group of acquired and potentially treatable myopathies. On the basis of unique clinical, histopathological, immunological, and demographic features, they can be differentiated
Hohlfeld, R. +2 more
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Back pain as the presenting symptom in juvenile dermato/polymyositis
Juvenile dermato/polymyositis is an inflammatory myopathy that usually presents with symmetrical hip and shoulder girdle muscle weakness, with or without a skin rash.
Cimaz R., Fink CW
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Platelet distribution width and disease activity in patients with polymyositis and dermatomyositis
Background: Polymyositis and dermatomyositis are inflammatory condition presents with distinct skin findings and varying degrees of systemic involvement with marked elevation of hepatic enzymes which serve as biomarkers. However hepatic markers and acute
Doaa Hussein Ahmed Hussein +3 more
doaj
Successful salvage therapy of intravenous cyclophosphamide for refractory polymyositis in an elderly patient: a case report. [PDF]
Dermatomyositis and polymyositis may affect children and adults and are now widely recognized as major causes of disability which, thanks to the introduction of immunosuppressive drugs, is often treatable, at least to some extent.
PINTO, Antonio +7 more
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