 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 |
|---|
| 2024 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2004 | 0 | 1 | 1 |
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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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Karaa A, Bertini E, Carelli V, Cohen B, Ennes GM, Falk MJ, Goldstein A, Gorman G, Haas R, Hirano M, Klopstock T, Koenig MK, Kornblum C, Lamperti C, Lehman A, Longo N, Molnar MJ, Parikh S, Phan H, Pitceathly RDS, Saneto R, Scaglia F, Servidei S, Tarnopolsky M, Toscano A, Van Hove JLK, Vissing J, Vockley J, Finman JS, Abbruscato A, Brown DA, Sullivan A, Shiffer JA, Mancuso M. Genotype-specific effects of elamipretide in patients with primary mitochondrial myopathy: a post hoc analysis of the MMPOWER-3 trial. Orphanet J Rare Dis. 2024 Nov 21; 19(1):431.
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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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