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Brain Communications|July 20, 2022
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementiaAlessandra Fanciulli, Fabian Leys, Fabienne Lehner, 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.Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 2021
The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α-Synuclein in PDGBAStefanie Lerche, Claudia Schulte, Isabel Wurster, et al.Parkinsonism & Related Disorders|January 15, 2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter studySara Ortega-Cubero, Oswaldo Lorenzo-Betancor, Elena Lorenzo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.The Lancet. Neurology|June 20, 2025
Diagnostic and prognostic value of α-synuclein seed amplification assay kinetic measures in Parkinson's disease: a longitudinal cohort studyChristina D Orrú, David P Vaughan, Nirosen Vijiaratnam, et al.Movement Disorders Clinical Practice|September 29, 2023
Development and Validation of a Prognostic Model to Predict Overall Survival in Multiple System AtrophySabine Eschlboeck, Georg Goebel, Christine Eckhardt, et al.Journal of Neurology|February 14, 2024
The comorbidity profiles and medication issues of patients with multiple system atrophy: a systematic cross-sectional analysisLan Ye, Stephan Greten, Florian Wegner, et al.Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD CohortEva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.Pageof 9