换一批摘要Idiopathic inflammatory myopathies (IIMs) are heterogeneous disorders characterized by chronic muscle weakness and muscle fatigue and mononuclear cell infiltration into skeletal muscle.[1] The most common subgroups in adults are dermatomyositis (DM), polymyositis (PM), amyopathic DM (ADM), inclusion body myositis (IBM), and juvenile DM (JDM). Several diagnostic or classification criteria for IIM have been developed.[2?5] Classification criteria are mostly used in research and clinical trials, not daily in practice. Great efforts have been dedicated in pursuing new criteria in the past decades.
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DOI
10.4103/0366-6999.246082
发布时间
2018-12-20（万方平台首次上网日期，不代表论文的发表时间）
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