Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Christopher M Gomez

Showing results (91-100 of 128) with videos related to

Pageof 13
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2024
Digital Measures of Postural Sway Quantify Balance Deficits in Spinocerebellar AtaxiaVrutangkumar V Shah, Daniel Muzyka, Adam Jagodinsky, et al.
Movement Disorders Clinical Practice|December 18, 2025
Digital Gait Measures Discriminate People with Friedreich's Ataxia from Healthy ControlsHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2024
Standing Balance Conditions and Digital Sway Measures for Clinical Trials of Friedreich's AtaxiaHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Human Molecular Genetics|September 25, 2012
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insultKatherine E Hekman, Guo-Yun Yu, Christopher D Brown, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Human Molecular Genetics|December 23, 2020
De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalusMaria J Nabais Sá, Alexandra N Olson, Grace Yoon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypesMiao Sun, Amy Knight Johnson, Viswateja Nelakuditi, et al.
The Lancet. Digital Health|October 17, 2025
Development and validation of a composite digital balance score for spinocerebellar ataxia: a prospective studyJames McNames, Vrutangkumar V Shah, Hannah L Casey, et al.
Journal of Neurology|June 19, 2013
Analysis of the visual system in Friedreich ataxiaLauren A Seyer, Kristin Galetta, James Wilson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 2, 2017
C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxiasKarla P Figueroa, Shi-Rui Gan, Susan Perlman, et al.
Pageof 13

Showing results (91-100 of 128) with videos related to

Sort By:
Pageof 13
Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2024
Digital Measures of Postural Sway Quantify Balance Deficits in Spinocerebellar AtaxiaVrutangkumar V Shah, Daniel Muzyka, Adam Jagodinsky, et al.
Movement Disorders Clinical Practice|December 18, 2025
Digital Gait Measures Discriminate People with Friedreich's Ataxia from Healthy ControlsHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2024
Standing Balance Conditions and Digital Sway Measures for Clinical Trials of Friedreich's AtaxiaHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Human Molecular Genetics|September 25, 2012
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insultKatherine E Hekman, Guo-Yun Yu, Christopher D Brown, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Human Molecular Genetics|December 23, 2020
De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalusMaria J Nabais Sá, Alexandra N Olson, Grace Yoon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypesMiao Sun, Amy Knight Johnson, Viswateja Nelakuditi, et al.
The Lancet. Digital Health|October 17, 2025
Development and validation of a composite digital balance score for spinocerebellar ataxia: a prospective studyJames McNames, Vrutangkumar V Shah, Hannah L Casey, et al.
Journal of Neurology|June 19, 2013
Analysis of the visual system in Friedreich ataxiaLauren A Seyer, Kristin Galetta, James Wilson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 2, 2017
C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxiasKarla P Figueroa, Shi-Rui Gan, Susan Perlman, et al.
Pageof 13