duchenne muscular dystrophy and glutathione Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Mitochondria and Reactive Oxygen Species:
Mitochondria and Reactive Oxygen Species: The Therapeutic Balance of Powers for Duchenne Muscular Dystrophy Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial enhancing compound Olesoxime American Journal of Physiology Cell Physiology American Physiological Society What is Duchenne? Frontiers Lipid peroxidation and sarcopenia: molecular mechanisms and potential therapeutic approaches
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