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2) Serdaroglu P, Deymeer F, Parman Y. Prevalence of sporadic inclusion body myositis(s-IBM) in Turkey: A muscle biopsy based survey. Neuromuscul Disord. 2007; 17: 849
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3) Needham M, Corbett A, Day T, et al. Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis. J Clin Neurosci. 2008; 15: 1350-3
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7) Needham M, James I, Corbett A, et al. Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases. J Neurol Neurosurg Psychiatry. 2008; 79: 1056-60
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9) Dalakas MC, Rakocevic G, Shatunov A, et al. Inclusion body myositis with human immunodeficiency virus infection: four cases with clonal expansion of viral-specific T cells. Ann Neurol. 2007; 61: 466-75
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10) Matsuura E, Umehara F, Nose H, et al. Inclusion body myositis associated with human T-lymphotropic virus-type I infection: eleven patients from an endemic area in Japan. J Neuropathol Exp Neurol. 2008; 67: 41-9
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11) Salajegheh M, Rakocevic G, Raju R, et al. T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositis. Neurology. 2007; 69: 1672-9
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13) Tateyama M, Fujihara K, Misu T, et al. CCR7+ myeloid dendritic cells together with CCR7+ T cells and CCR7+ macrophages invade CCL19+ nonnecrotic muscle fibers in inclusion body myositis. J Neurol Sci. 2009; 279: 47-52
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14) Greenberg SA, Sanoudou D, Haslett JN, et al. Molecular profiles of inflammatory myopathies. Neurology. 2002; 59: 1170-82
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15) Schmidt J, Barthel K, Wrede A, et al. Interrelation of inflammation and APP in sIBM: IL-1β induces accumulation of β-amyloid in skeletal muscle. Brain. 2008; 131(Pt 5): 1228-40
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16) Kitazawa M, Trinh DN, LaFerla FM. Inflammation induces tau pathology in inclusion body myositis model via glycogen synthase kinase-3β. Ann Neurol. 2008; 64: 15-24
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17) Olivé M, Janué A, Moreno D, et al. TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies. J Neuropathol Exp Neurol. 2009; 68: 262-73
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18) Terracciano C, Nogalska A, Engel WK, et al. In inclusion-body myositis muscle fibers Parkinson-associated DJ-1 is increased and oxidized. Free Radic Biol Med. 2008; 45: 773-9
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19) Vattemi G, Nogalska A, King Engel W, et al. Amyloid-β42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis. Acta Neuropathol. 2009; 117: 569-74
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20) Jayaraman M, Kannayiram G, Rajadas J. Amyloid toxicity in skeletal myoblasts: Implications for inclusion-body myositis. Arch Biochem Biophys. 2008; 474: 15-21
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21) Shtifman A, Ward CW, Laver DR, et al. Amyloid-β protein impairs Ca(2+) release and contractility in skeletal muscle. Neurobiol Aging. 2008 Dec 22. [Epub ahead of print]
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22) Askanas V, McFerrin J, Alvarez RB, et al. β APP gene transfer into cultured human muscle induces inclusion-body myositis aspects. Neuroreport. 1997; 8: 2155-8
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23) Li J, Yin C, Okamoto H, et al. Proteomic analysis of inclusion body myositis. J Neuropathol Exp Neurol. 2006; 65: 826-33
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24) Hutchinson DO, Jongbloed B. Two-dimensional gel electrophoresis in inclusion body myositis. J Clin Neurosci. 2008; 15: 440-4
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25) Banwell BL, Engel AG. αB-crystallin immunolocalization yields new insights into inclusion body myositis. Neurology. 2000; 54: 1033-41
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26) Wojcik S, Engel WK, McFerrin J, et al. AβPP-overexpression and proteasome inhibition increase αB-crystallin in cultured human muscle: relevance to inclusion-body myositis. Neuromuscul Disord. 2006; 16: 839-44
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27) Lünemann JD, Schmidt J, Schmid D, et al. β-amyloid is a substrate of autophagy in sporadic inclusion body myositis. Ann Neurol. 2007; 61: 476-83
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28) Lünemann JD, Schmidt J, Dalakas MC, et al. Macroautophagy as a pathomechanism in sporadic inclusion body myositis. Autophagy. 2007; 3: 384-6
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31) McFerrin J, Engel WK, Askanas V. Cultured inclusion-body myositis muscle fibers do not accumulate β-amyloid precursor protein and can be innervated. Neurology. 1999; 53: 2184-7
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33) Wojcik S, Nogalska A, McFerrin J, et al. Myostatin precursor protein is increased and associates with amyloid-β precursor protein in inclusion-body myositis culture model. Neuropathol Appl Neurobiol. 2007; 33: 238-42
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34) Nogalska A, Wojcik S, Engel WK, et al. Endoplasmic reticulum stress induces myostatin precursor protein and NF-κB in cultured human muscle fibers: relevance to inclusion body myositis. Exp Neurol. 2007; 204: 610-8
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35) McFarlane C, Hennebry A, Thomas M, et al. Myostatin signals through Pax7 to regulate satellite cell self-renewal. Exp Cell Res. 2008; 314: 317-29
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36) Chen X, Ghribi O, Geiger JD. Rabbits fed cholesterol-enriched diets exhibit pathological features of inclusion body myositis. Am J Physiol Regul Integr Comp Physiol. 2008; 294: 829-35
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37) Barohn RJ, Amato AA, Sahenk Z, et al. Inclusion body myositis: explanation for poor response to immunosuppressive therapy. Neurology. 1995; 45: 1302-4
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38) Griggs RC. The current status of treatment for inclusion-body myositis. Neurology. 2006; 66(2 Suppl 1): S30-2
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39) Dastmalchi M, Grundtman C, Alexanderson H, et al. A high incidence of disease flares in an open pilot study of infliximab in patients with refractory inflammatory myopathies. Ann Rheum Dis. 2008; 67: 1670-7
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40) Lindberg C, Trysberg E, Tarkowski A, et al. Anti-T-lymphocyte globulin treatment in inclusion body myositis: a randomized pilot study. Neurology. 2003; 61: 260-2
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41) Dalakas MC, Rakocevic G, Schmidt J, et al. Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis. Brain. 2009; 132(Pt 6): 1536-44
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42) Kitazawa M, Vasilevko V, Cribbs DH, et al. Immunization with amyloid-β attenuates inclusion body myositis-like myopathology and motor impairment in a transgenic mouse model. J Neurosci. 2009; 29: 6132-41
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43) Bogdanovich S, Krag TO, Barton ER, et al. Functional improvement of dystrophic muscle by myostatin blockade. Nature. 2002; 420: 418-21
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44) Wagner KR, Fleckenstein JL, Amato AA, et al. A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy. Ann Neurol. 2008; 63: 561-71
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45) Rodino-Klapac LR, Haidet AM, Kota J, et al. Inhibition of myostatin with emphasis on follistatin as a therapy for muscle disease. Muscle Nerve. 2009; 39: 283-96
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