"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 |
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1997 | 2 | 0 | 2 |
1998 | 2 | 1 | 3 |
2000 | 2 | 1 | 3 |
2001 | 1 | 1 | 2 |
2003 | 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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Mitochondrial dysfunction in myofibrillar myopathy. Neuropathol Appl Neurobiol. 2003 Feb; 29(1):45-51.
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Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum. J Neuropathol Exp Neurol. 2001 Nov; 60(11):1032-40.
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Control of oxidative phosphorylation in skeletal muscle. Biochim Biophys Acta. 2001 Mar 01; 1504(1):12-9.
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Flux control of cytochrome c oxidase in human skeletal muscle. J Biol Chem. 2000 Sep 08; 275(36):27741-5.
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New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. J Neuropathol Exp Neurol. 2000 May; 59(5):353-60.
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Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle. Biochem Soc Trans. 2000 Feb; 28(2):159-64.
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mtDNA depletion and impairment of mitochondrial function in a case of a multisystem disorder including severe myopathy. J Inherit Metab Dis. 1998 Jun; 21(4):400-8.
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Oxygen dependence of flux control of cytochrome c oxidase -- implications for mitochondrial diseases. FEBS Lett. 1998 Jan 23; 422(1):33-5.
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Use of saponin-permeabilized muscle fibers for the diagnosis of mitochondrial diseases. Biofactors. 1998; 7(3):221-3.
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Detection of mitochondrial defects by laser fluorimetry. Mol Cell Biochem. 1997 Sep; 174(1-2):97-100.