Mitochondrial Myopathies
"Mitochondrial Myopathies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of muscle diseases associated with abnormal mitochondria function.
Descriptor ID |
D017240
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MeSH Number(s) |
C05.651.460 C10.668.491.500 C18.452.660.560
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Concept/Terms |
Luft Disease- Luft Disease
- Disease, Luft
- Luft's Disease
- Disease, Luft's
- Lufts Disease
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Below are MeSH descriptors whose meaning is more general than "Mitochondrial Myopathies".
Below are MeSH descriptors whose meaning is more specific than "Mitochondrial Myopathies".
This graph shows the total number of publications written about "Mitochondrial Myopathies" by people in UAMS Profiles by year, and whether "Mitochondrial Myopathies" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2020 | 1 | 0 | 1 | 2017 | 1 | 0 | 1 | 2015 | 2 | 0 | 2 | 2012 | 1 | 0 | 1 | 2008 | 1 | 0 | 1 | 2007 | 1 | 0 | 1 | 2004 | 2 | 1 | 3 |
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Below are the most recent publications written about "Mitochondrial Myopathies" by people in Profiles over the past ten years.
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Riley LG, Rudinger-Thirion J, Frugier M, Wilson M, Luig M, Alahakoon TI, Nixon CY, Kirk EP, Roscioli T, Lunke S, Stark Z, Wierenga KJ, Palle S, Walsh M, Higgs E, Arbuckle S, Thirukeswaran S, Compton AG, Thorburn DR, Christodoulou J. The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Hum Mutat. 2020 08; 41(8):1425-1434.
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Sommerville EW, Ng YS, Alston CL, Dallabona C, Gilberti M, He L, Knowles C, Chin SL, Schaefer AM, Falkous G, Murdoch D, Longman C, de Visser M, Bindoff LA, Rawles JM, Dean JCS, Petty RK, Farrugia ME, Haack TB, Prokisch H, McFarland R, Turnbull DM, Donnini C, Taylor RW, Gorman GS. Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy. JAMA Neurol. 2017 06 01; 74(6):686-694.
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Rocha MC, Grady JP, Gr?newald A, Vincent A, Dobson PF, Taylor RW, Turnbull DM, Rygiel KA. A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis. Sci Rep. 2015 Oct 15; 5:15037.
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Payne BA, Gardner K, Blakely EL, Maddison P, Horvath R, Taylor RW, Chinnery PF. Clinical and pathological features of mitochondrial DNA deletion disease following antiretroviral treatment. JAMA Neurol. 2015 May; 72(5):603-5.
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