Inclusion body myositis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
http://link.springer.com/content/pdf/10.1007/s11940-000-0019-9.pdf
Reference28 articles.
1. Amato AA, Barohn RJ: Idiopathic inflammatory myopathies. Neurol Clin 1997, 15:615–648. A good review of the three most frequent forms of idiopathic inflammatory myopathy: dermatomyositis, polymyositis, and inclusion body myositis.
2. Carpenter S: Inclusion body myositis, a review. J Neuropathol Exp Neurol 1996, 55:1105–1114.
3. Askanas V, Serratrice G, Engel WK, ed: Inclusion-Body Myositis and Myopathies. Cambridge, UK: Cambridge University Press; 1998.
4. Griggs RC, Askanas V, DiMauro S, et al.: Inclusion body myositis and myopathies. Ann Neurol 1995, 38:705–713. Summary of the international workshop on inclusion body myositis held in Jupiter Beach, Florida, in 1995. Diagnostic criteria for sporadic inclusion body myositis were proposed.
5. Amato AA, Gronseth GS, Jackson CE, et al.: Inclusion body myositis: clinical and pathological boundaries. Ann Neurol 1995, 40:581–586. The authors point out that patients with “steroid-resistant polymyositis” frequently have the typical pattern of weakness seen in inclusion body myositis (IBM), even if the classic morphologic findings are not seen in the initial muscle biopsy specimen. The authors labeled the disorder in this group as “possible” or “probable” IBM. Often, a second or third muscle biopsy is needed to confirm the diagnosis.
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