Inclusion body myositis: an underdiagnosed myopathy of older people-Reference-Cited by-同舟云学术

Inclusion body myositis: an underdiagnosed myopathy of older people

Published:2006-01-01 Issue:1 Volume:35 Page:91-94
ISSN:1468-2834
Container-title:Age and Ageing
language:en
Short-container-title:

Author:

Munshi Sunil K.,Thanvi Bhomraj,Jonnalagadda S. J.,Da Forno Philip,Patel Ashish,Sharma Saroo

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing,General Medicine

Link

http://academic.oup.com/ageing/article-pdf/35/1/91/73807/afj014.pdf

Reference11 articles.

1. The very long list of references supporting this article has meant that only the ten most important are listed here and are represented by bold type throughout the text. The full list of references is available in the supplementary data on the journal’s website (http://www.ageing.oxfordjournals.org) along with a description of the diagnostic criteria and mechanisms and the theories of pathogenesis of IBM (Appendices II and III).

2. Askanas V , Engel WK. Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: diseases of oxidative stress and aging? Arch Neurol 1998; 55: 915–20.

3. Amato AA , Gronseth GS, Jackson CE et al. Inclusion body myositis: clinical and pathological boundaries. Ann Neurol 1996; 40: 581–6.

4. Dalakas MC. Polymyositis, dermatomyositis and inclusion-body myositis. N Engl J Med 1991; 325: 1487–98.

5. Griggs RC , Askanas V, DiMauro S et al. Inclusion body myositis and myopathies. Ann Neurol 1995; 38: 705–13.

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