Proteomic study of sporadic inclusion body myositis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Biochemistry
Link
http://link.springer.com/content/pdf/10.1186/s12953-014-0045-2.pdf
Reference22 articles.
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2. Needham M, Mastaglia FL: Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches. Lancet Neurol 2007, 6: 620–631. 10.1016/S1474-4422(07)70171-0
3. Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C: Mitochondrial abnormalities in inclusion-body myositis. Neurology 2006, 66: S49-S55. 10.1212/01.wnl.0000192127.63013.8d
4. Askanas V, Engel WK: Inclusion-body myositis: a myodegenerative conformational disorder associated with Aβ, protein-misfolding and proteasome inhibition. Neurology 2006, 66: S39-S48. 10.1212/01.wnl.0000192128.13875.1e
5. Hutchinson DO, Jongbloed B: Two-dimensional gel electrophoresis in inclusion body myositis. J Clin Neurosci 2008, 15: 440–444. 10.1016/j.jocn.2007.03.006
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