Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies
The incidence of mitochondrial encephalomyopathies
in childhood: Clinical features and morphological, biochemical, and DNA anbormalities.
One randomized, double-blind clinical trial that used a combination of creatine monohydrate, coenzyme Q10, and alpha-lipoic acid lowered markers of oxidative stress in people with mitochondrial cytopathies while creatine monohydrate used alone in patients with mitochondrial encephalomyopathies
enhanced aerobic oxidative function of the mitochondria.
While childhood-onset mitochondrial encephalomyopathies
are usually severe, relentlessly progressive conditions with fatal outcome, this syndrome stands out by showing complete (or almost complete) spontaneous recovery.
and related syndromes: brief review.
Studies on mitochondrial oxidative phosphorylation in permeabilized human skin fibroblasts: application to mitochondrial encephalomyopathies
Leu(UUR)] gene associated with MELAS subgroup of mitochondrial encephalomyopathies
Audiological evaluation in Chinese patients with mitochondrial encephalomyopathies