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

Sheng Di

Showing results (361-370 of 374) with videos related to

Pageof 38
Sort By:
BMC Research Notes|January 31, 2014
Chinese culture permeation in the treatment of Parkinson disease: a cross-sectional study in four regions of ChinaZhen-Xin Zhang, Honglei Chen, Sheng-Di Chen, et al.
Scientific Reports|March 24, 2017
Phenotype of postural instability/gait difficulty in Parkinson disease: relevance to cognitive impairment and mechanism relating pathological proteins and neurotransmittersLi-Jun Zuo, Ying-Shan Piao, Li-Xia Li, et al.
BMC Neurology|January 19, 2018
Clinical features and dysfunctions of iron metabolism in Parkinson disease patients with hyper echogenicity in substantia nigra: a cross-sectional studyShu-Yang Yu, Chen-Jie Cao, Li-Jun Zuo, et al.
BMC Medicine|November 6, 2022
Speech silence character as a diagnostic biomarker of early cognitive decline and its functional mechanism: a multicenter cross-sectional cohort studyHua-Long Wang, Ran Tang, Ru-Jing Ren, et al.
Journal of Clinical and Translational Hepatology|November 1, 2021
Metabolic Disorders Combined with Noninvasive Tests to Screen Advanced Fibrosis in Nonalcoholic Fatty Liver DiseaseYi-Wen Shi, Fang-Ping He, Jin-Jun Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2018
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patientsWo-Tu Tian, Xiao-Jun Huang, Xiao Mao, et al.
American Journal of Human Genetics|November 13, 2012
A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigreeWang-Yang Xu, Ming-Min Gu, Lian-Hua Sun, et al.
Brain Imaging and Behavior|July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathyFei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.
Scientific Reports|April 27, 2017
Serotonergic dysfunctions and abnormal iron metabolism: Relevant to mental fatigue of Parkinson diseaseLi-Jun Zuo, Shu-Yang Yu, Yang Hu, et al.
Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Pageof 38

Showing results (361-370 of 374) with videos related to

Sort By:
Pageof 38
BMC Research Notes|January 31, 2014
Chinese culture permeation in the treatment of Parkinson disease: a cross-sectional study in four regions of ChinaZhen-Xin Zhang, Honglei Chen, Sheng-Di Chen, et al.
Scientific Reports|March 24, 2017
Phenotype of postural instability/gait difficulty in Parkinson disease: relevance to cognitive impairment and mechanism relating pathological proteins and neurotransmittersLi-Jun Zuo, Ying-Shan Piao, Li-Xia Li, et al.
BMC Neurology|January 19, 2018
Clinical features and dysfunctions of iron metabolism in Parkinson disease patients with hyper echogenicity in substantia nigra: a cross-sectional studyShu-Yang Yu, Chen-Jie Cao, Li-Jun Zuo, et al.
BMC Medicine|November 6, 2022
Speech silence character as a diagnostic biomarker of early cognitive decline and its functional mechanism: a multicenter cross-sectional cohort studyHua-Long Wang, Ran Tang, Ru-Jing Ren, et al.
Journal of Clinical and Translational Hepatology|November 1, 2021
Metabolic Disorders Combined with Noninvasive Tests to Screen Advanced Fibrosis in Nonalcoholic Fatty Liver DiseaseYi-Wen Shi, Fang-Ping He, Jin-Jun Chen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2018
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patientsWo-Tu Tian, Xiao-Jun Huang, Xiao Mao, et al.
American Journal of Human Genetics|November 13, 2012
A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigreeWang-Yang Xu, Ming-Min Gu, Lian-Hua Sun, et al.
Brain Imaging and Behavior|July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathyFei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.
Scientific Reports|April 27, 2017
Serotonergic dysfunctions and abnormal iron metabolism: Relevant to mental fatigue of Parkinson diseaseLi-Jun Zuo, Shu-Yang Yu, Yang Hu, et al.
Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.
Pageof 38