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Mitochondrial encephalomyopathies, with episodes

MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) resuits from a point mutation in the mitochondriai tRNA gene. [Pg.191]

L12. Liou, C. W., Huang, C. C., Lin, T. K., Tsai, J. L., and Wei, Y. H., Correction of pancreatic /3-cell dysfunction with coenzyme Qio in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome and diabetes mellitus. Eur. Neurol. 43, 54-55 (2000). [Pg.122]

Figure 8-4. The effect of the MELAS mutation on mitochondrial function is to interfere with function of respiratory Complex I or I and IV, leading to increased levels of NADH and thus also of lactate. CoQ, coenzyme Q MELAS, mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes RC, respiratory complex. Figure 8-4. The effect of the MELAS mutation on mitochondrial function is to interfere with function of respiratory Complex I or I and IV, leading to increased levels of NADH and thus also of lactate. CoQ, coenzyme Q MELAS, mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes RC, respiratory complex.

See other pages where Mitochondrial encephalomyopathies, with episodes is mentioned: [Pg.31]    [Pg.269]    [Pg.270]    [Pg.706]    [Pg.84]    [Pg.93]    [Pg.90]    [Pg.90]    [Pg.539]    [Pg.471]    [Pg.268]   
See also in sourсe #XX -- [ Pg.100 ]




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Mitochondrial encephalomyopathies, with

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