| http://www.w3.org/ns/prov#value | - There were no statistical associations in either the overall group or in the separate idiopathic inflammatory myopathies (DM and PM) between the CAM and no-CAM groups when other signs and symptoms were analyzed, including peak creatine kinase, dysphagia, interstitial lung disease, and treatment response, or when dermatologic features were analyzed in DM (skin necrosis, heliotrope rash, Gottron sig
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