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Grace Yoon

Showing results (111-120 of 177) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4-Related Hereditary Spastic ParaplegiaJulian E Alecu, Afshin Saffari, Marvin Ziegler, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Movement Disorders Clinical Practice|November 9, 2020
Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar AtrophyLaurence Gauquelin, Taila Hartley, Mark Tarnopolsky, et al.
Life Science Alliance|July 6, 2021
PNKP is required for maintaining the integrity of progenitor cell populations in adult miceWisoo Shin, Whitney Alpaugh, Laura J Hallihan, et al.
Parkinsonism & Related Disorders|April 29, 2022
Genetic, structural and clinical analysis of spastic paraplegia 4Parizad Varghaei, Mehrdad A Estiar, Setareh Ashtiani, et al.
Journal of Child Neurology|April 3, 2018
Impact of Mobility Device Use on Quality of Life in Children With Friedreich AtaxiaResham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Human Mutation|October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxiaSarah L Sawyer, Jeremy Schwartzentruber, Chandree L Beaulieu, et al.
Journal of Neurodevelopmental Disorders|May 17, 2014
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problemsSébastien Chénier, Grace Yoon, Bob Argiropoulos, et al.
Nature|December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.
The EMBO Journal|September 11, 2020
Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self-renewal of colonic stem and progenitor cellsHuajun Han, Laurie A Davidson, Yang-Yi Fan, et al.
Pageof 18

Showing results (111-120 of 177) with videos related to

Sort By:
Pageof 18
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4-Related Hereditary Spastic ParaplegiaJulian E Alecu, Afshin Saffari, Marvin Ziegler, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Movement Disorders Clinical Practice|November 9, 2020
Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar AtrophyLaurence Gauquelin, Taila Hartley, Mark Tarnopolsky, et al.
Life Science Alliance|July 6, 2021
PNKP is required for maintaining the integrity of progenitor cell populations in adult miceWisoo Shin, Whitney Alpaugh, Laura J Hallihan, et al.
Parkinsonism & Related Disorders|April 29, 2022
Genetic, structural and clinical analysis of spastic paraplegia 4Parizad Varghaei, Mehrdad A Estiar, Setareh Ashtiani, et al.
Journal of Child Neurology|April 3, 2018
Impact of Mobility Device Use on Quality of Life in Children With Friedreich AtaxiaResham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Human Mutation|October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxiaSarah L Sawyer, Jeremy Schwartzentruber, Chandree L Beaulieu, et al.
Journal of Neurodevelopmental Disorders|May 17, 2014
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problemsSébastien Chénier, Grace Yoon, Bob Argiropoulos, et al.
Nature|December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.
The EMBO Journal|September 11, 2020
Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self-renewal of colonic stem and progenitor cellsHuajun Han, Laurie A Davidson, Yang-Yi Fan, et al.
Pageof 18