Search research articles
Contact Us
Filters
Showing results (131-140 of 137) with videos related to
Page
of 14
Sort By:
You have reached the last page of results.
This site can display upto 137 results.
Annals of Neurology
|
September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy
Linlin Wan, Zhao Chen, Na Wan, et al.
Frontiers in Aging Neuroscience
|
July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study
Yun Peng, Linliu Peng, Zhao Chen, et al.
Plos One
|
December 7, 2013
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia
Yuting Shi, Junling Wang, Jia-Da Li, et al.
Neurobiology of Disease
|
June 7, 2026
The fT3/fT4 ratio as a candidate marker of motor progression in SCA3
Mengyuan Dong, Ziyan Ding, Zhao Chen, et al.
Neurology
|
April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3
Linliu Peng, Zhao Chen, Zhe Long, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 6, 2023
Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography
Zhao Chen, Guang Liao, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 29, 2020
Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine Learning
Linliu Peng, Zhao Chen, Tiankai Chen, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 137) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 137 results.
Annals of Neurology
|
September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy
Linlin Wan, Zhao Chen, Na Wan, et al.
Frontiers in Aging Neuroscience
|
July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study
Yun Peng, Linliu Peng, Zhao Chen, et al.
Plos One
|
December 7, 2013
Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia
Yuting Shi, Junling Wang, Jia-Da Li, et al.
Neurobiology of Disease
|
June 7, 2026
The fT3/fT4 ratio as a candidate marker of motor progression in SCA3
Mengyuan Dong, Ziyan Ding, Zhao Chen, et al.
Neurology
|
April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3
Linliu Peng, Zhao Chen, Zhe Long, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 6, 2023
Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography
Zhao Chen, Guang Liao, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 29, 2020
Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine Learning
Linliu Peng, Zhao Chen, Tiankai Chen, et al.
Page
of 14