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Neurodegenerative Disease Management|June 29, 2022
Friedreich ataxia: clinical features and new developmentsMedina Keita, Kellie McIntyre, Layne N Rodden, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2023
A Novel Metric for Predicting Severity of Disease Features in Friedreich's AtaxiaLayne N Rodden, Christian Rummey, Sudha Kessler, et al.BMC Neurology|January 13, 2016
Friedreich Ataxia and nephrotic syndrome: a series of two patientsJulianna E Shinnick, Charles J Isaacs, Sharon Vivaldi, et al.Annals of Clinical and Translational Neurology|July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxiaAngela D Bhalla, Alireza Khodadadi-Jamayran, Yanjie Li, et al.Human Molecular Genetics|December 28, 2018
GRP75 overexpression rescues frataxin deficiency and mitochondrial phenotypes in Friedreich ataxia cellular modelsYi Na Dong, Emily McMillan, Elisia M Clark, et al.Annals of Clinical and Translational Neurology|July 13, 2026
Stem Cell Transplantation in Friedreich Ataxia: Cure for Leukemia but No Effect on Neurological ProgressionAlexandra Gitman, Niyati Bhandari, Maria Castellaro, et al.Annals of Clinical and Translational Neurology|August 17, 2017
Selected missense mutations impair frataxin processing in Friedreich ataxiaElisia Clark, Jill S Butler, Charles J Isaacs, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 17, 2009
Clinical measures of dysarthria in Friedreich AtaxiaArunjot Singh, Elizabeth Epstein, Lauren M Myers, et al.Journal of Neurology|July 23, 2011
Assessment of neurological efficacy of idebenone in pediatric patients with Friedreich's ataxia: data from a 6-month controlled study followed by a 12-month open-label extension studyThomas Meier, Susan L Perlman, Christian Rummey, et al.Frontiers in Neuroscience|December 13, 2021
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable FXN ReactivationLayne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.Pageof 24