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Journal of Movement Disorders|September 26, 2019
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian SyndromesMartina Bocchetta, Juan Eugenio Iglesias, Viorica Chelban, et al.
Neurology. Genetics|August 13, 2019
<i>MAPT</i> p.V363I mutation: A rare cause of corticobasal degenerationSarah Ahmed, Monica Diez Fairen, Marya S Sabir, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 13, 2019
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsyEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2022
Combining biomarkers for prognostic modelling of Parkinson's diseaseNirosen Vijiaratnam, Michael Lawton, Amanda J Heslegrave, et al.
The Lancet. Neurology|December 20, 2020
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association studyEdwin Jabbari, Shunsuke Koga, Rebecca R Valentino, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2024
Evaluation of Cerebrospinal Fluid α-Synuclein Seed Amplification Assay in Progressive Supranuclear Palsy and Corticobasal SyndromeDavid P Vaughan, Riona Fumi, Marte Theilmann Jensen, et al.
Brain : a Journal of Neurology|April 13, 2026
Data-driven modelling of tau pathology reveals distinct progressive supranuclear palsy subtypesPatrick W Cullinane, Jacy Bezerra Parmera, Hemanth Nelvagal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 18, 2025
Treatment Selection and Prioritization for the EJS ACT-PD MAMS Trial PlatformCristina Gonzalez-Robles, Dilan Athauda, Thomas R Barber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 28, 2020
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's DiseaseManuela M X Tan, Michael A Lawton, Edwin Jabbari, et al.
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