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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 2 |
2013 | 1 |
2014 | 2 |
2024 | 0 |
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6 results
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Page 1
Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM gene.
Muscle Nerve. 2014 Aug;50(2):292-5. doi: 10.1002/mus.24262.
Muscle Nerve. 2014.
PMID: 24711008
Free PMC article.
Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.
Weiduschat N, Kaufmann P, Mao X, Engelstad KM, Hinton V, DiMauro S, De Vivo D, Shungu D.
Weiduschat N, et al.
Neurology. 2014 Mar 4;82(9):798-805. doi: 10.1212/WNL.0000000000000169. Epub 2014 Jan 29.
Neurology. 2014.
PMID: 24477106
Free PMC article.
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Mitochondrial encephalomyopathies--fifty years on: the Robert Wartenberg Lecture.
DiMauro S.
DiMauro S.
Neurology. 2013 Jul 16;81(3):281-91. doi: 10.1212/WNL.0b013e31829bfe89.
Neurology. 2013.
PMID: 23858410
Free PMC article.
No abstract available.
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A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.
Ash DB, Papadimitriou D, Hays AP, Dimauro S, Hirano M.
Ash DB, et al.
Arch Neurol. 2012 Sep;69(9):1190-2. doi: 10.1001/archneurol.2011.2600.
Arch Neurol. 2012.
PMID: 22964912
Free PMC article.
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CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.
Hirano M, Garone C, Quinzii CM.
Hirano M, et al.
Biochim Biophys Acta. 2012 May;1820(5):625-31. doi: 10.1016/j.bbagen.2012.01.006. Epub 2012 Jan 18.
Biochim Biophys Acta. 2012.
PMID: 22274133
Free PMC article.
Review.
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Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy.
Garone C, Tadesse S, Hirano M.
Garone C, et al.
Brain. 2011 Nov;134(Pt 11):3326-32. doi: 10.1093/brain/awr245. Epub 2011 Sep 20.
Brain. 2011.
PMID: 21933806
Free PMC article.
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