"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
|
| MeSH Number(s) |
C05.651.460 C10.668.491.500 C18.452.660.560
|
| Concept/Terms |
Luft Disease- Luft Disease
- Disease, Luft
- Luft's Disease
- Disease, Luft's
- Lufts Disease
|
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 this website by year, and whether "Mitochondrial Myopathies" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mitochondrial Myopathies" by people in Profiles.
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Lopez-Gomez C, Sanchez-Quintero MJ, Lee EJ, Kleiner G, Tadesse S, Xie J, Akman HO, Gao G, Hirano M. Synergistic Deoxynucleoside and Gene Therapies for Thymidine Kinase 2 Deficiency. Ann Neurol. 2021 10; 90(4):640-652.
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Miles MV, Miles L, Tang PH, Horn PS, Steele PE, DeGrauw AJ, Wong BL, Bove KE. Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies. Mitochondrion. 2008 Mar; 8(2):170-80.
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Miles L, Wong BL, Dinopoulos A, Morehart PJ, Hofmann IA, Bove KE. Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods. Hum Pathol. 2006 Feb; 37(2):173-84.
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Franklin JA, Lalikos JF, Wooden WA. A case of mitochondrial myopathy and cleft palate. Cleft Palate Craniofac J. 2005 May; 42(3):327-30.
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Andreu AL, Bruno C, Shanske S, Shtilbans A, Hirano M, Krishna S, Hayward L, Systrom DS, Brown RH, DiMauro S. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy. Neurology. 1998 Nov; 51(5):1444-7.