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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.Movement Disorders : Official Journal of the Movement Disorder Society|August 12, 2015
Diffusion imaging of nigral alterations in early Parkinson's disease with dopaminergic deficitsNorbert Schuff, I-Wei Wu, Shannon Buckley, 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.Neurology. Genetics|June 24, 2022
Genome Sequencing in the Parkinson Disease ClinicEmily J Hill, Laurie A Robak, Rami Al-Ouran, et al.Annals of Neurology|June 11, 2015
Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trialC Warren Olanow, Raymond T Bartus, Tiffany L Baumann, et al.Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2008
Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing resultsChristopher G Goetz, Barbara C Tilley, Stephanie R Shaftman, et al.The Lancet. Neurology|October 26, 2010
Gene delivery of AAV2-neurturin for Parkinson's disease: a double-blind, randomised, controlled trialWilliam J Marks, Raymond T Bartus, Joao Siffert, et al.Molecular Genetics & Genomic Medicine|May 16, 2019
Autosomal dominant mitochondrial membrane protein-associated neurodegeneration (MPAN)Allison Gregory, Mitesh Lotia, Suh Young Jeong, et al.JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.Pageof 58