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Original Article

Mitochondrial abnormalities in extraocular muscles in myotonic dystrophy

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Pages 115-122 | Published online: 08 Jul 2009

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Read on this site (1)

>Ryuichi Osanai, Masanobu Kinoshita & Kazuhiko Hirose. (2007) Eye movement disorders in myotonic dystrophy type 1. Acta Oto-Laryngologica 127:sup559, pages 78-84.
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Articles from other publishers (8)

Andrew I. Mikhail, Sean Y. Ng, Stephanie R. Mattina & Vladimir Ljubicic. (2023) AMPK is mitochondrial medicine for neuromuscular disorders. Trends in Molecular Medicine 29:7, pages 512-529.
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Andrew I. Mikhail, Alexander Manta, Sean Y. Ng, Aislin K. Osborne, Stephanie R. Mattina, Mark R. Mackie & Vladimir Ljubicic. (2023) A single dose of exercise stimulates skeletal muscle mitochondrial plasticity in myotonic dystrophy type 1. Acta Physiologica 237:4.
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Andrew I. Mikhail, Peter L. Nagy, Katherine Manta, Nicholas Rouse, Alexander Manta, Sean Y. Ng, Michael F. Nagy, Paul Smith, Jian-Qiang Lu, Joshua P. Nederveen, Vladimir Ljubicic & Mark A. Tarnopolsky. (2022) Aerobic exercise elicits clinical adaptations in myotonic dystrophy type 1 patients independently of pathophysiological changes. Journal of Clinical Investigation 132:10.
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Flemming Wibrand, Tina D. Jeppesen, Anja L. Frederiksen, David B. Olsen, Morten Duno, Marianne Schwartz & John Vissing. (2010) Limited diagnostic value of enzyme analysis in patients with mitochondrial tRNA mutations. Muscle & Nerve 41:5, pages 607-613.
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G Siciliano, M Mancuso, D Tedeschi, M.L Manca, M.R Renna, V Lombardi, A Rocchi, F Martelli & L Murri. (2001) Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy. Brain Research Bulletin 56:3-4, pages 405-410.
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Noriyuki Nakamura, Nobutaka Hattori, Masashi Tanaka & Yoshikuni Mizuno. (1996) Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 1308:3, pages 215-221.
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G. Siciliano, P. Viacava, B. Rossi, D. Andreani, A. Muratorio & G. Bevilacqua. (1992) Ocular myopathy without ophthalmoplegia can be a form of mitochondrial myopathy. Clinical Neurology and Neurosurgery 94:2, pages 133-141.
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Jan P. ter Bruggen, Cees C. Tijssen, Han G. Brunner, Bernard A. van Oost & Louis A. K. Bastiaensen. (2004) Eye movement disorder: An early expression of the myotonic dystrophy gene?. Muscle & Nerve 15:3, pages 358-361.
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