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10.1212/01.CON.0000511070.50715.ab http://scihub22266oqcxt.onion/10.1212/01.CON.0000511070.50715.ab C5898966!5898966 !27922497     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27922497 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Continuum+(Minneap+Minn) 2016 ; 22 (6, Muscle and Neuromuscular Junction Disorders ): 1852-1870 Nephropedia Template TP {{tp|p=27922497 |t=2016. Autoimmune Myopathies |pdf=|usr=}}{{27922497 }} gab.com Text Autoimmune Myopathies JO: Continuum (Minneap Minn) http://www.kidney.de/pget.php?&tw=1&pmid=27922497 #FOAvip PURPOSE OF REVIEW: This article provides guidelines for diagnosing and treating the different subtypes of autoimmune myopathies. RECENT FINDINGS: The most common subtypes of autoimmune myopathies are dermatomyositis, immune-mediated necrotizing myopathy, antisynthetase syndrome, and overlap syndromes; isolated polymyositis is an exceptionally rare disease. Specific autoantibodies are associated with unique clinical phenotypes and may be used for diagnostic and prognostic purposes, such as to assess the risk of coexisting malignancy. SUMMARY: Diagnosing the specific subtype of autoimmune myopathy can be achieved by combining relevant features of the history, neuromuscular examination, muscle biopsy, and serologic studies. Twit Text FOAVip Autoimmune Myopathies ????Continuum (Minneap Minn) http://www.kidney.de/pget.php?&tw=1&pmid=27922497 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27922497 #FOAvip English Wikipedia <ref>{{Cite pmid|27922497 }}</ref> Autoimmune Myopathies #MMPMID27922497 Mammen AL Continuum (Minneap Minn) 2016[Dec]; 22 (6, Muscle and Neuromuscular Junction Disorders ): 1852-1870 PMID27922497 show ga PURPOSE OF REVIEW: This article provides guidelines for diagnosing and treating the different subtypes of autoimmune myopathies. RECENT FINDINGS: The most common subtypes of autoimmune myopathies are dermatomyositis, immune-mediated necrotizing myopathy, antisynthetase syndrome, and overlap syndromes; isolated polymyositis is an exceptionally rare disease. Specific autoantibodies are associated with unique clinical phenotypes and may be used for diagnostic and prognostic purposes, such as to assess the risk of coexisting malignancy. SUMMARY: Diagnosing the specific subtype of autoimmune myopathy can be achieved by combining relevant features of the history, neuromuscular examination, muscle biopsy, and serologic studies. |Aged [MESH] |Autoantibodies/blood [MESH] |Autoimmune Diseases/blood/*diagnosis/therapy [MESH] |Dermatomyositis/blood/*diagnosis/therapy [MESH] |Electromyography/methods [MESH] |Female [MESH] |Humans [MESH] |Male [MESH] |Middle Aged [MESH] |Muscular Diseases/blood/diagnosis/therapy [MESH]Autoimmune Myopathies (epmc).pdf DeepDyve Pubget Overpricing