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

Linlin Wan

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Neurology|August 21, 2020
Association of serum neurofilament light and disease severity in patients with spinocerebellar ataxia type 3Yun Peng, Youming Zhang, Zhao Chen, et al.
Translational Psychiatry|September 18, 2021
CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cellsLang He, Shang Wang, Linliu Peng, et al.
Journal of Neurology|May 15, 2023
Diagnostic and prognostic performance of plasma neurofilament light chain in multiple system atrophy: a cross-sectional and longitudinal studyLinliu Peng, Linlin Wan, Mingjie Liu, et al.
Annals of Neurology|September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System AtrophyLinlin Wan, Zhao Chen, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2026
Nongenetic Factors Associated with Age at Onset and Disease Severity in Spinocerebellar Ataxia Type 3: A Cross-Sectional Cohort StudyJiawei He, Zhao Chen, Linyi Zeng, et al.
Orphanet Journal of Rare Diseases|November 27, 2024
Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of AmericaEmma Rybalka, Hyung Jun Park, Atchayaram Nalini, et al.
Frontiers in Aging Neuroscience|July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort StudyYun Peng, Linliu Peng, Zhao Chen, et al.
Neurobiology of Disease|June 7, 2026
The fT3/fT4 ratio as a candidate marker of motor progression in SCA3Mengyuan Dong, Ziyan Ding, Zhao Chen, et al.
Neurology|April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3Linliu 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 TomographyZhao Chen, Guang Liao, Na Wan, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Neurology|August 21, 2020
Association of serum neurofilament light and disease severity in patients with spinocerebellar ataxia type 3Yun Peng, Youming Zhang, Zhao Chen, et al.
Translational Psychiatry|September 18, 2021
CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cellsLang He, Shang Wang, Linliu Peng, et al.
Journal of Neurology|May 15, 2023
Diagnostic and prognostic performance of plasma neurofilament light chain in multiple system atrophy: a cross-sectional and longitudinal studyLinliu Peng, Linlin Wan, Mingjie Liu, et al.
Annals of Neurology|September 17, 2020
Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System AtrophyLinlin Wan, Zhao Chen, Na Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2026
Nongenetic Factors Associated with Age at Onset and Disease Severity in Spinocerebellar Ataxia Type 3: A Cross-Sectional Cohort StudyJiawei He, Zhao Chen, Linyi Zeng, et al.
Orphanet Journal of Rare Diseases|November 27, 2024
Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of AmericaEmma Rybalka, Hyung Jun Park, Atchayaram Nalini, et al.
Frontiers in Aging Neuroscience|July 22, 2022
The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort StudyYun Peng, Linliu Peng, Zhao Chen, et al.
Neurobiology of Disease|June 7, 2026
The fT3/fT4 ratio as a candidate marker of motor progression in SCA3Mengyuan Dong, Ziyan Ding, Zhao Chen, et al.
Neurology|April 24, 2021
New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3Linliu 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 TomographyZhao Chen, Guang Liao, Na Wan, et al.
Pageof 7