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

Yo-Tsen Liu

Showing results (31-40 of 54) with videos related to

Pageof 6
Sort By:
Plos One|January 28, 2016
Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary NeuropathyCheng-Tsung Hsiao, Pei-Chien Tsai, Chou-Ching Lin, et al.
Annals of Clinical and Translational Neurology|November 16, 2016
Clinical and biophysical characterization of 19 <i>GJB1</i> mutationsPei-Chien Tsai, De-Ming Yang, Yi-Chu Liao, et al.
Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.
Biomedical Journal|June 6, 2022
The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopiaYan-Ting Lu, Chung-Yao Hsu, Yo-Tsen Liu, et al.
European Radiology|August 8, 2023
Magnetic resonance radiomics-derived sphericity correlates with seizure in brain arteriovenous malformationsJih-Yuan Lin, Chia-Feng Lu, Yong-Sin Hu, et al.
Scientific Reports|January 10, 2026
Knowledge graph representation of the mappings between seizure semiology and epileptogenic zonesShihao Yang, Zirui Wen, Wenxin Zhan, et al.
Oncotarget|May 14, 2016
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defectsYo-Tsen Liu, Fang-Shin Nian, Wan-Ju Chou, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Neurology|July 11, 2014
Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathyYo-Tsen Liu, Matilde Laurá, Joshua Hersheson, et al.
Cellular and Molecular Neurobiology|December 29, 2022
Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome SequencingLi-Hsin Chang, Nai-Fang Chi, Chun-Yu Chen, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Plos One|January 28, 2016
Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary NeuropathyCheng-Tsung Hsiao, Pei-Chien Tsai, Chou-Ching Lin, et al.
Annals of Clinical and Translational Neurology|November 16, 2016
Clinical and biophysical characterization of 19 <i>GJB1</i> mutationsPei-Chien Tsai, De-Ming Yang, Yi-Chu Liao, et al.
Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.
Biomedical Journal|June 6, 2022
The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopiaYan-Ting Lu, Chung-Yao Hsu, Yo-Tsen Liu, et al.
European Radiology|August 8, 2023
Magnetic resonance radiomics-derived sphericity correlates with seizure in brain arteriovenous malformationsJih-Yuan Lin, Chia-Feng Lu, Yong-Sin Hu, et al.
Scientific Reports|January 10, 2026
Knowledge graph representation of the mappings between seizure semiology and epileptogenic zonesShihao Yang, Zirui Wen, Wenxin Zhan, et al.
Oncotarget|May 14, 2016
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defectsYo-Tsen Liu, Fang-Shin Nian, Wan-Ju Chou, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.
Neurology|July 11, 2014
Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathyYo-Tsen Liu, Matilde Laurá, Joshua Hersheson, et al.
Cellular and Molecular Neurobiology|December 29, 2022
Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome SequencingLi-Hsin Chang, Nai-Fang Chi, Chun-Yu Chen, et al.
Pageof 6