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Neurogenetics|June 19, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseEva C Schulte, Brit Mollenhauer, Alexander Zimprich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2016
Validation of conversion between mini-mental state examination and montreal cognitive assessmentMichael Lawton, Meike Kasten, Margaret T May, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2024
Basic Science in Movement Disorders: Fueling the Engine of Translation into Clinical PracticeTiago F Outeiro, Lorraine V Kalia, Erwan Bezard, et al.
Neurology|May 11, 2016
Monitoring of 30 marker candidates in early Parkinson disease as progression markersBrit Mollenhauer, Johannes Zimmermann, Friederike Sixel-Döring, et al.
Parkinsonism & Related Disorders|February 21, 2021
Clinically relevant copy-number variants in exome sequencing data of patients with dystoniaMichael Zech, Sylvia Boesch, Matej Škorvánek, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2008
GATA transcription factors directly regulate the Parkinson's disease-linked gene alpha-synucleinClemens R Scherzer, Jeffrey A Grass, Zhixiang Liao, et al.
Cold Spring Harbor Molecular Case Studies|September 29, 2018
A unique de novo gain-of-function variant in CAMK4 associated with intellectual disability and hyperkinetic movement disorderMichael Zech, Daniel D Lam, Sandrina Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2021
Cerebrospinal α-Synuclein Oligomers Reflect Disease Motor Severity in DeNoPa Longitudinal CohortNour K Majbour, Ilham Y Abdi, Mohammed Dakna, et al.
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