Inclusion body myositis: a case with associated collagen vascular disease responding to treatment.
Open Access
- 1 March 1985
- journal article
- case report
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 48 (3) , 270-273
- https://doi.org/10.1136/jnnp.48.3.270
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.Keywords
This publication has 7 references indexed in Scilit:
- Inclusion body myositis (IBM)Neurology, 1983
- Inclusion Body MyositisArchives of Neurology, 1982
- Inclusion body myositisJournal of the Neurological Sciences, 1982
- Inclusion Body Myositis Associated With Sjogren's SyndromeArchives of Neurology, 1982
- Inclusion body myositisNeurology, 1978
- Ultrastructural studies in human polymyositisJournal of the Neurological Sciences, 1975
- Myxovirus-like structures and accompanying nuclear changes in chronic polymyositis.1968