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Annals of Medicine Volume 45, 2013 - Issue 1
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Review Article

Diagnosis and treatment of mitochondrial myopathies

Gerald PfefferInstitute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom;Clinician Investigator Program, University of British Columbia, Vancouver, Canada
&
Patrick F. ChinneryInstitute of Genetic Medicine, Newcastle University, Newcastle, United KingdomCorrespondence[email protected]
Pages 4-16 | Received 01 Aug 2011, Accepted 15 Aug 2011, Published online: 25 Aug 2011

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Aleksandrina S Volobueva, Alexandra A Melnichenko, Andrey V Grechko & Alexander N Orekhov. (2018) Mitochondrial genome variability: the effect on cellular functional activity. Therapeutics and Clinical Risk Management 14, pages 237-245.
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Ying Zhou, Jianhua Yi, Li Liu, Xiaoping Wang, Liang Dong & Ailian Du. (2018) Acute mitochondrial myopathy with respiratory insufficiency and motor axonal polyneuropathy. International Journal of Neuroscience 128:3, pages 231-236.
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David H. Jang, Matthew Kelly, Kevin Hardy, David S. Lambert, Frances S. Shofer & David M. Eckmann. (2017) A preliminary study in the alterations of mitochondrial respiration in patients with carbon monoxide poisoning measured in blood cells. Clinical Toxicology 55:6, pages 579-584.
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K. Van Driessche, R. Ducatelle, K. Chiers, R. Van Coster & J. H. van der Kolk. (2015) Ultrastructural mitochondrial alterations in Equine myopathies of unknown origin. Veterinary Quarterly 35:1, pages 2-8.
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Emna Mkaouar-Rebai, Afif Ben Mahmoud, Imen Chamkha, Imen Chabchoub, Thouraya Kammoun, Mongia Hachicha & Faiza Fakhfakh. (2014) A novel MT-CO2 m.8249G > A pathogenic variation and the MT-TW m.5521G > A mutation in patients with mitochondrial myopathy. Mitochondrial DNA 25:5, pages 394-399.
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