"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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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 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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A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy. Hum Mutat. 1994; 3(1):37-43.
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Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation"). Neurology. 1993 Jun; 43(6):1200-6.