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Epilepsy & Behavior : E&B|March 4, 2017
The current status of artisanal cannabis for the treatment of epilepsy in the United StatesDustin Sulak, Russell Saneto, Bonni GoldsteinACS Chemical Biology|May 6, 2025
Selective Small-Molecule Activator of Patient-Derived GPX4 VariantHengrui Liu, Farhad Forouhar, Russell Saneto, et al.Mitochondrion|September 26, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and managementSumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.Pediatric Neurology|September 22, 2022
Sleep and Breathing Disturbances in Children With Leigh Syndrome: A Comparative StudyJia-Der Ju Wang, Maida Chen, Cristian Zhang, et al.American Journal of Medical Genetics. Part A|October 20, 2017
Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical developmentSavannah Michels, Kimberly Foss, Kaylee Park, et al.Molecular Genetics & Genomic Medicine|January 7, 2020
Functional analysis of a novel mutation in the TIMM8A gene that causes deafness-dystonia-optic neuronopathy syndromeAddison Neighbors, Tonya Moss, Lynda Holloway, et al.Current Treatment Options in Neurology|November 7, 2009
A modern approach to the treatment of mitochondrial diseaseSumit Parikh, Russell Saneto, Marni J Falk, et al.Nature Chemical Biology|December 21, 2021
Characterization of a patient-derived variant of GPX4 for precision therapyHengrui Liu, Farhad Forouhar, Tobias Seibt, et al.Epilepsia|July 19, 2025
Phase 1 study of ABI-009 (nab-rapamycin) for surgically refractory epilepsy (RaSuRE)Koko Hall, Russell Saneto, Stephanie Randle, et al.Neurology|February 20, 2025
Adult-onset Leigh Syndrome: An analysis of the North American Mitochondrial Disease Consortium Database (P3-11.017)Emanuele Barca, Adam Kroopnick, Alexander Houck, et al.Pageof 2