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

Chun-Hwei Tai

Showing results (31-40 of 70) with videos related to

Pageof 7
Sort By:
Neurobiology of Aging|July 8, 2015
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese populationKai-Hsiang Chen, Ruey-Meei Wu, Hang-I Lin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2010
Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptomsRwei-Ling Yu, Ruey-Meei Wu, Chun-Hwei Tai, et al.
Journal of Parkinson'S Disease|May 24, 2020
The Development of the Social Functioning Scale for Patients with Parkinson's DiseaseFang-Te Su, Chun-Hwei Tai, Chun-Hsiang Tan, et al.
Neurobiology of Aging|January 29, 2013
Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese populationChin-Hsien Lin, Meng-Ling Chen, Tzu-Ting Lai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 19, 2007
Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonismChin-Hsien Lin, Wuh-Liang Hwu, Shu-Chuan Chiang, et al.
Stem Cell Research|January 31, 2021
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 geneChih-Hsin Ou-Yang, Chun-Hwei Tai, Han-Yi Lin, et al.
Physical Therapy|October 16, 2010
Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with Parkinson diseaseSheau-Ling Huang, Ching-Lin Hsieh, Ruey-Meei Wu, et al.
European Journal of Neurology|December 28, 2021
Amantadine treatment and delayed onset of levodopa-induced dyskinesia in patients with early Parkinson's diseaseChi-Chuan Wang, Tsai-Ling Wu, Fang-Ju Lin, et al.
Neuropsychiatric Disease and Treatment|December 5, 2015
The impact of nonmotor symptoms on quality of life in patients with Parkinson's disease in TaiwanWeng-Ming Liu, Ru-Jen Lin, Rwei-Ling Yu, et al.
Annals of Neurology|October 5, 2012
Subthalamic discharges as a causal determinant of parkinsonian motor deficitsChun-Hwei Tai, Ming-Kai Pan, Janice Janing Lin, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Neurobiology of Aging|July 8, 2015
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese populationKai-Hsiang Chen, Ruey-Meei Wu, Hang-I Lin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2010
Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptomsRwei-Ling Yu, Ruey-Meei Wu, Chun-Hwei Tai, et al.
Journal of Parkinson'S Disease|May 24, 2020
The Development of the Social Functioning Scale for Patients with Parkinson's DiseaseFang-Te Su, Chun-Hwei Tai, Chun-Hsiang Tan, et al.
Neurobiology of Aging|January 29, 2013
Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese populationChin-Hsien Lin, Meng-Ling Chen, Tzu-Ting Lai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 19, 2007
Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonismChin-Hsien Lin, Wuh-Liang Hwu, Shu-Chuan Chiang, et al.
Stem Cell Research|January 31, 2021
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 geneChih-Hsin Ou-Yang, Chun-Hwei Tai, Han-Yi Lin, et al.
Physical Therapy|October 16, 2010
Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with Parkinson diseaseSheau-Ling Huang, Ching-Lin Hsieh, Ruey-Meei Wu, et al.
European Journal of Neurology|December 28, 2021
Amantadine treatment and delayed onset of levodopa-induced dyskinesia in patients with early Parkinson's diseaseChi-Chuan Wang, Tsai-Ling Wu, Fang-Ju Lin, et al.
Neuropsychiatric Disease and Treatment|December 5, 2015
The impact of nonmotor symptoms on quality of life in patients with Parkinson's disease in TaiwanWeng-Ming Liu, Ru-Jen Lin, Rwei-Ling Yu, et al.
Annals of Neurology|October 5, 2012
Subthalamic discharges as a causal determinant of parkinsonian motor deficitsChun-Hwei Tai, Ming-Kai Pan, Janice Janing Lin, et al.
Pageof 7