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Entzündliche, endokrine und toxische Muskelerkrankungen

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Klinische Neurologie

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Literatur

Zitierte Literatur

  • Argov Z, Tiram E, Eisenberg I et al. (1997) Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1. Ann Neurol 41: 548–551

    Article  CAS  PubMed  Google Scholar 

  • Beyenburg S, Zierz S, Jerusalem F (1994) Einschusstkörpermyositis. Akt Neurol 21: 77–83

    Google Scholar 

  • Bohan A, Peter JB, Bowman RL, Pearson CM (1977) A computer-assisted analysis of 153 patients with polymyositis and dermatomyositis. Medicine (Baltimore) 56: 255–286

    CAS  PubMed  Google Scholar 

  • Bronner IM, Linssen WHJP, van der Meulen MF et al. (2004) Polymyositis: an ongoing discussion about a disease entity. Arch Neurol 61: 132–135

    Article  PubMed  Google Scholar 

  • Brouwer R, Hengstman GJD, Vree Egberts W et al. (2001) Autoantibody profiles in the sera of European patients with myositis. Ann Rheum Dis 60: 116–123

    Article  CAS  PubMed  Google Scholar 

  • Dalakas MC (1991) Polymyositis, dermatomyositis, and inclusion-body myositis. N Engl J Med 325: 1487–1498

    CAS  PubMed  Google Scholar 

  • Dalakas MC (1992 a) Clinical, immunopathologic, and therapeutic considerations of inflammatory myopathies. Clin Neuropharmacol 15: 327–351

    CAS  PubMed  Google Scholar 

  • Dalakas MC (1992 b) Inflammatory and toxic myopathies. Curr Opin Neurol 5: 645–654

    CAS  Google Scholar 

  • Dalakas MC (1992 c) Inflammatory myopathies: pathogenesis and treatment. Neuropharmacology 5: 327–351

    Google Scholar 

  • Dalakas MC (1992 d) Inflammatory myopathies. In: Rowland LP, Di-Mauro S (eds) Myopathies. Elsevier, Amsterdam (Handbook of clinical neurology, vol 18, pp 369–390)

    Google Scholar 

  • Dalakas MC, Illa I, Dambrosia JM et al. (1993) A controlled trial of highdose intravenous immune globuline infusions as treatment for dermatomyositis. N Engl J Med 329: 1993–2000

    Article  CAS  PubMed  Google Scholar 

  • Dalakas MC, Sonies B, Dambrosia J, Sekul E, Cupler E, Sivakumar K (1997) Treatment of inclusion-body myositis with IVIG: a doubleblind, placebo-controlled study. Neurology 48: 712–716

    CAS  PubMed  Google Scholar 

  • De Vere R, Bradley WG (1975) Polymyositis: its presentation, morbidity and mortality. Brain 98: 637–666

    Google Scholar 

  • Eisenberg I, Hochner H, Shemesh M et al. (2001) Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13. Eur J Hum Genet 9: 501–509

    Article  CAS  PubMed  Google Scholar 

  • Hengstman GJD, van Engelen BGM, van Venrooij WJ (2004) Myositis specific autoantibodies: changing insights in pathophysiology and clinical associations. Curr Opin Rheumatol 16: 69–699

    Google Scholar 

  • Jerusalem F, Zierz S (1991) Muskelerkrankungen. Thieme, Stuttgart New York

    Google Scholar 

  • Kayashima T, Matsuo H, Satoh A et al. (2002) Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE). J Hum Genet 47: 77–79

    Article  CAS  PubMed  Google Scholar 

  • Kissel JT, Mendell JR, Rammohan KW (1986) Microvascular deposition of complement membrane attack complex in dermatomyositis. N Engl J Med 314: 329–334

    CAS  PubMed  Google Scholar 

  • Lotz BP, Engel AG, Nishino H, Stevens JC, Litchy WJ (1989) Inclusion body myositis. Brain 112: 727–742

    PubMed  Google Scholar 

  • Martinsson T, Darin N, Kyllermann M et al. (1999) Dominant hereditary inclusion body myopathy gene (IBM3) maps to chromosome region 17p13.1. Am J Hum Genet 64: 1420–1426

    Article  CAS  PubMed  Google Scholar 

  • Martinsson T, Oldfords A, Darin N et al. (2000) Autosomal dominant myopathy: missense mutation (Glu-706 → Lys) in the myosin heavy chain Iia gene. Proc Natl Acad Sci USA 97: 14614–14619

    Article  CAS  PubMed  Google Scholar 

  • Moosmann B, Behl C (2004) Selenoprotein synthesis and side-effects of statins. Lancet 363: 892–894

    Article  CAS  PubMed  Google Scholar 

  • Pearson CM, Currie S (1974) Polymyositis and related disorders. In: Walton JN (ed) Disorders of voluntary muscle, 3rd edn. Churchill Livingstone, Edinburgh

    Google Scholar 

  • van der Meulen MF, Bronner IM Hoogendijk JE et al. (2003) Polymyositis: an overdiagnosed entity. Neurology 61: 316–321

    PubMed  Google Scholar 

  • Vasconcelos OM, Raju R, Dalakas MC (2002) GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBM. Neurology 59: 1776–1779

    CAS  PubMed  Google Scholar 

Weiterführende Literatur

  • Engel AG, Franzini-Armstrong C (1994) Myology. McGraw-Hill, New York

    Google Scholar 

  • Kissel JT, Mendell JR (1992) The endocrine myopathies. In: Rowland LP, DiMauro S (eds) Myopathies. Elsevier, Amsterdam (Handbook of clinical neurology, vol 18)

    Google Scholar 

  • Mastaglia FL (1992) Toxic myopathies. In: Rowland LP, DiMauro S (eds) Myopathies. Elsevier, Amsterdam (Handbook of clinical neurology, vol 18)

    Google Scholar 

  • Pongratz DE, Reimers CD, Hahn D, Nägele M, Müller-Felber W (1990) Atlas der Muskelkrankheiten. Urban & Schwarzenberg, München

    Google Scholar 

  • Walton J, Karpati G, Hilton-Jones D (1994) Disorders of voluntary muscle. Churchill Livingstone, Edinburgh

    Google Scholar 

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Traufeller, K., Zierz, S. (2006). Entzündliche, endokrine und toxische Muskelerkrankungen. In: Berlit, P. (eds) Klinische Neurologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-31176-9_11

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  • DOI: https://doi.org/10.1007/3-540-31176-9_11

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-01982-4

  • Online ISBN: 978-3-540-31176-8

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