Abstract
Patients with inclusion body myositis demonstrate characteristic histological and electronmicroscopical abnormalities in muscle and are generally considered refractory to treatment. A patient with inclusion body myositis is described with evidence of associated autoimmune disease, who responded to steroids.
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CITATION STYLE
APA
Lane, R. J. M., Fulthorpe, J. J., & Hudgson, P. (1985). Inclusion body myositis: A case with associated collagen vascular disease responding to treatment. Journal of Neurology Neurosurgery and Psychiatry, 48(3), 270–273. https://doi.org/10.1136/jnnp.48.3.270
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