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Cells|July 25, 2025
Discovery of N-(6-Methoxypyridin-3-yl)quinoline-2-amine Derivatives for Imaging Aggregated α-Synuclein in Parkinson's Disease with Positron Emission TomographyHaiyang Zhao, Tianyu Huang, Dhruva D Dhavale, et al.Neurology. Genetics|April 29, 2016
Clinical and genetic features of cervical dystonia in a large multicenter cohortMark S LeDoux, Satya R Vemula, Jianfeng Xiao, et al.Journal of the American College of Radiology : JACR|May 6, 2017
ACR Appropriateness Criteria® Cerebrovascular Disease, Michael B Salmela, Shabnam Mortazavi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2011
The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystoniaJianfeng Xiao, Yu Zhao, Robert W Bastian, et al.Science Translational Medicine|April 29, 2026
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological diseaseDaniel Western, Chengran Yang, Jigyasha Timsina, et al.Annals of Clinical and Translational Neurology|March 25, 2022
Hold that pose: capturing cervical dystonia's head deviation severity from videoZheng Zhang, Elizabeth Cisneros, Ha Yeon Lee, et al.Ebiomedicine|May 30, 2025
Impact of Y chromosome loss on the risk of Parkinson's disease and progressionJunhao Wang, Xinyi Chen, Wenxuan Du, et al.Journal of the Neurological Sciences|November 7, 2020
It's tricky: Rating alleviating maneuvers in cervical dystoniaElizabeth Cisneros, Glenn T Stebbins, Qiyu Chen, et al.Human Molecular Genetics|December 8, 2007
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's diseaseYonghong Li, Andrew Grupe, Charles Rowland, et al.Brain and Behavior|July 22, 2021
Non-motor phenotypic subgroups in adult-onset idiopathic, isolated, focal cervical dystoniaMegan E Wadon, Grace A Bailey, Zehra Yilmaz, et al.Pageof 56