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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 Paraplegia
Julian E Alecu, Afshin Saffari, Marvin Ziegler, et al.
Neurology. Genetics
|
February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating Scale
Christian 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 Atrophy
Laurence 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 mice
Wisoo Shin, Whitney Alpaugh, Laura J Hallihan, et al.
Parkinsonism & Related Disorders
|
April 29, 2022
Genetic, structural and clinical analysis of spastic paraplegia 4
Parizad 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 Ataxia
Resham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Human Mutation
|
October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxia
Sarah 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 problems
Sébastien Chénier, Grace Yoon, Bob Argiropoulos, et al.
Nature
|
December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia
Nicolas 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 cells
Huajun Han, Laurie A Davidson, Yang-Yi Fan, et al.
Page
of 18
Search research articles
Search
Showing results (111-120 of 177) with videos related to
Sort By:
Page
of 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 Paraplegia
Julian E Alecu, Afshin Saffari, Marvin Ziegler, et al.
Neurology. Genetics
|
February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating Scale
Christian 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 Atrophy
Laurence 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 mice
Wisoo Shin, Whitney Alpaugh, Laura J Hallihan, et al.
Parkinsonism & Related Disorders
|
April 29, 2022
Genetic, structural and clinical analysis of spastic paraplegia 4
Parizad 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 Ataxia
Resham Ejaz, Shiyi Chen, Charles J Isaacs, et al.
Human Mutation
|
October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxia
Sarah 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 problems
Sébastien Chénier, Grace Yoon, Bob Argiropoulos, et al.
Nature
|
December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia
Nicolas 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 cells
Huajun Han, Laurie A Davidson, Yang-Yi Fan, et al.
Page
of 18