Idiopathic inflammatory myopathy and non-coding RNA [PDF]
Frontiers in Immunology, 2023 Idiopathic inflammatory myopathies (IIMs) are common autoimmune diseases that affect skeletal muscle quality and function. The lack of an early diagnosis and treatment can lead to irreversible muscle damage.
Yang Yang +5 more
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Study on advances in the association between autoantibodies and clinical phenotypes in idiopathic inflammatory myopathy [PDF]
Zhenduanxue lilun yu shijian, 2022 Myositis specific autoantibodies(MSA) are important for the diagnosis and classification of idiopathic inflammatory myopathy (IIM). It reveales that there is a close relationship between various types of MSA and unique clinical manifestations as well as ...
ZHANG Hao, CHI Huihui, SU Yutong, YANG Chengde
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Functioning in adult patients with idiopathic inflammatory myopathy: Exploring the role of environmental factors using focus groups. [PDF]
PLoS ONE, 2021 ObjectiveHealth-related quality of life is impaired in idiopathic inflammatory myopathies. This study aimed to identify the main areas of the health-related quality of life environment domain that are affected in patients with myositis.MethodsA ...
I Armadans-Tremolosa +4 more
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History of diagnosis on idiopathic inflammatory myopathy
Chinese Journal of Contemporary Neurology and Neurosurgery, 2016 The idiopathic inflammatory myopathy (IIM) is a group of clinically heterogeneous, autoimmune-mediated disorders characterized by inflammation of muscle, elevated creatine kinase (CK), interstitial lung disease and other organ systems involvement ...
Wei ZHANG
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Coexistence of Axial Spondyloarthritis and Idiopathic Inflammatory Myopathy
Case Reports in Rheumatology, 2020 Both axial spondyloarthritis (axSpA) and idiopathic inflammatory myopathy (IIM) are infrequent, and their coexistence is even rarer; there are a few reported cases in the literature.
Yongpeng Ge, Linrong He
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Idiopathic Inflammatory Myopathies [PDF]
Seminars in Neurology, 2009 The idiopathic inflammatory myopathies are a group of rare disorders including polymyositis (PM), dermatomyositis (DM), and autoimmune necrotizing myopathies (NMs). The idiopathic inflammatory myopathies share many similarities. They present acutely, subacutely, or chronically with marked proximal and symmetric muscle weakness, except for associated ...
Mazen M, Dimachkie, Richard J, Barohn
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Reclassification of Korean patients with polymyositis and dermatomyositis based on the Bohan and Peter criteria by the 2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies [PDF]
The Korean Journal of Internal Medicine, 2021 Background/Aims We investigated the concordance rate of the classification of polymyositis (PM) and dermatomyositis (DM) between the Bohan and Peter criteria and the 2017 European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR ...
Juyoung Yoo +5 more
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Idiopathic inflammatory myopathies [PDF]
Vnitřní lékařství, 2018 Idiopathic inflammatory myopathies form a heterogeneous group of acquired inflammatory diseases afflicting striated muscles. The disease is frequently accompanied by systemic and organ involvement. Dermatomyositis, polymyositis, cancer associated myositis, immune mediated necrotizing myopathy, myositis in overlap syndromes, juvenile myositis and ...
Parker, Matthew +3 more
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Idiopathic inflammatory myopathies: a review [PDF]
Internal Medicine Journal, 2021 AbstractIdiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap myositis (OM), sporadic inclusion body myositis (IBM) and necrotising autoimmune myopathy (NAM), also known as immune‐mediated necrotising myopathy.
Catherine Ashton +4 more
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Reumatismo, 2023 We read with interest the article by Camargo-Coronel et al. reporting on a systematic review of patients with idiopathic, inflammatory myopathy developing after anti-SARS-CoV-2 vaccinations.
J. Finsterer +2 more
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