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Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy
Christoffer Rasmus Vissing
,
Morten Dunø
,
Flemming Wibrand
,
Mette Christensen
,
John Vissing
Afdeling for Hjerne- og Nervesygdomme
Afdeling for Genetik
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Alfabetisk
Medicin og biovidenskab
Mitochondrial Myopathies
100%
acylcarnitine
95%
Biomarkers
44%
Acyl-CoA Dehydrogenase
19%
Electron Transport
13%
Mitochondrial RNA
9%
Genotype
8%
Inborn Errors Metabolism
7%
Muscles
7%
Phenotype
7%
Mutation
6%
Transfer RNA
6%
Tandem Mass Spectrometry
6%
Denmark
6%
Mitochondrial DNA
6%
High Pressure Liquid Chromatography
5%
Cohort Studies
4%
Prospective Studies
3%
Proteins
2%
Kemi
Biological Marker
61%
Mutation
57%
Neuromuscular
47%
Transfer RNA
45%
Tandem Mass Spectrometry
28%
Pharmacological Metabolism
26%
Error
25%
Plasma
20%
Protein
14%