Sporadic inclusion body myositis (S-IBM) is a progressive, acquired disease of unknown etiology. Prior studies have suggested neurogenic involvement based on electrophysiologic data, although the biopsy is compatible with a myopathic process. Quantitative electrophysiologic studies were performed in
Electrophysiological spectrum of inclusion body myositis
โ Scribed by Juan L. Joy; Dr. Shin J. Oh; Ali I. Baysal
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 282 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0148-639X
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A patient with inclusion body niyositis was treated with a course of 22 leukocytaphereses combined with prednisone and azathioprine therapy. He improved clinically during an induction phase of frequent cytapheresis, which reduced the circulating levels of T lymphocytes and monocytes and decreased th
## Abstract Sporadic inclusion body myositis is the commonest acquired disease of skeletal muscles after 50 years of age, and as such it has commanded a great deal of attention of investigators over the past 25 years. As a result, a large amount of information has accumulated concerning its clinica