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Annals of Clinical and Translational Neurology
|
July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxia
Angela 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 models
Yi Na Dong, Emily McMillan, Elisia M Clark, 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 Ataxia
Layne N Rodden, Christian Rummey, Sudha Kessler, et al.
Annals of Clinical and Translational Neurology
|
August 17, 2017
Selected missense mutations impair frataxin processing in Friedreich ataxia
Elisia 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 Ataxia
Arunjot 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 study
Thomas Meier, Susan L Perlman, Christian Rummey, et al.
Frontiers in Neuroscience
|
December 13, 2021
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable <i>FXN</i> Reactivation
Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Neurobiology of Disease
|
December 12, 2013
Cortical synaptic NMDA receptor deficits in α7 nicotinic acetylcholine receptor gene deletion models: implications for neuropsychiatric diseases
Hong Lin, Fu-Chun Hsu, Bailey H Baumann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 10, 2012
Anti-NMDA receptor encephalitis antibody binding is dependent on amino acid identity of a small region within the GluN1 amino terminal domain
Amy J Gleichman, Lynn A Spruce, Josep Dalmau, et al.
Journal of Child Neurology
|
July 4, 2012
Clinical monitoring in a patient with Friedreich ataxia and osteogenic sarcoma
Eric C Deutsch, Lauren A Seyer, Susan L Perlman, et al.
Page
of 26
Search research articles
Search
Showing results (71-80 of 251) with videos related to
Sort By:
Page
of 26
Annals of Clinical and Translational Neurology
|
July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxia
Angela 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 models
Yi Na Dong, Emily McMillan, Elisia M Clark, 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 Ataxia
Layne N Rodden, Christian Rummey, Sudha Kessler, et al.
Annals of Clinical and Translational Neurology
|
August 17, 2017
Selected missense mutations impair frataxin processing in Friedreich ataxia
Elisia 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 Ataxia
Arunjot 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 study
Thomas Meier, Susan L Perlman, Christian Rummey, et al.
Frontiers in Neuroscience
|
December 13, 2021
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable <i>FXN</i> Reactivation
Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, et al.
Neurobiology of Disease
|
December 12, 2013
Cortical synaptic NMDA receptor deficits in α7 nicotinic acetylcholine receptor gene deletion models: implications for neuropsychiatric diseases
Hong Lin, Fu-Chun Hsu, Bailey H Baumann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 10, 2012
Anti-NMDA receptor encephalitis antibody binding is dependent on amino acid identity of a small region within the GluN1 amino terminal domain
Amy J Gleichman, Lynn A Spruce, Josep Dalmau, et al.
Journal of Child Neurology
|
July 4, 2012
Clinical monitoring in a patient with Friedreich ataxia and osteogenic sarcoma
Eric C Deutsch, Lauren A Seyer, Susan L Perlman, et al.
Page
of 26