## Abstract The pathogenic role of inflammation in inclusion body myositis (IBM) remains uncertain. A 63βyearβold man developed a severe, rapidly progressive myopathy with clinical features typical of dermatomyositis (DM), but muscle pathology was typical of IBM. Treatment with prednisone and metho
Inclusion body myositis: Clinical and pathological boundaries
β Scribed by Dr. Anthony A. Amato; Gary S. Gronseth; Carlayne E. Jackson; Gil I. Wolfe; Jon S. Katz; Wilson W. Bryan; Richard J. Barohn
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 629 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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## Abstract We summarize the molecular phenotype, diagnostic criteria, and the newest advances related to seeking the pathogenic mechanism(s) of sporadic inclusionβbody myositis (sβIBM), a muscle disease usually of persons over age 50. On the basis of our research, several processes seem to be impo
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