Art
J-GLOBAL ID:202002220451564153   Reference number:20A1745262

A rare case of inclusion body myositis associated with anti-PM/Scl-75 antibodies

抗PM/Scl-75抗体が陽性であった封入体筋炎の1例
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Material:
Volume: 60  Issue:Page: 264-267(J-STAGE)  Publication year: 2020 
JST Material Number: U0602A  ISSN: 1882-0654  Document type: Article
Article type: 短報  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Drug therapy(=pharmacotherapy)for musculoskeletal diseases  ,  Treatment for immunologic diseases,allergic diseases. 
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Reference (12):
  • 1) Dalakas MC. High-dose intravenous immunoglobulin in inflammatory myopathies: experience based on controlled clinical trials. Neurol Sci 2003;24:S256-S259.
  • 2) Rose MR, ENMC IBM Working Group. 188th ENMC international workshop: inclusion body myositis, 2-4 December 2011, Naarden, The Netherlands. Neuromuscul Disord 2013;23:1044-1055.
  • 3) Hanke K, Bruckner CS, Dahnrich C, et al. Antibodies against PM/Scl-75 and PM/Scl-100 are independent markers for different subsets of systemic sclerosis patients. Arthritis Res Ther 2009;11:R22.
  • 4) Mahler M, Rajimakers R. Novel aspects of autoantibodies to the PM/Scl complex: clinical, genetic and diagnostic insights. Autoimmun Rev 2007;6:432-437.
  • 5) Greenberg SA. Cytoplasmic 5’-nucleotide autoantibodies in inclusion body myositis: isotypes and diagnostic utility. Muscle Nerve 2014;50:488-492.
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