Last Updated: 09/26/2026
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Found 7 publications
Japanese Leigh syndrome case treated with EPI-743.
Journal: Brain & development
Published: June 16, 2017
Comparing EPI-743 treatment in siblings with Leber's hereditary optic neuropathy mt14484 mutation.
Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie
Published: April 06, 2013
Glutathione: a redox signature in monitoring EPI-743 therapy in children with mitochondrial encephalomyopathies.
Journal: Molecular genetics and metabolism
Published: January 31, 2013
Brain uptake of Tc99m-HMPAO correlates with clinical response to the novel redox modulating agent EPI-743 in patients with mitochondrial disease.
Journal: Molecular genetics and metabolism
Published: September 24, 2012
EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome.
Journal: Molecular genetics and metabolism
Published: September 04, 2012
Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathy.
Journal: Archives of neurology
Published: March 14, 2012
Showing 1-7 of 7
Last Updated: 09/26/2026