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Archives of Neurology|October 11, 2002
Effects of coenzyme Q10 in early Parkinson disease: evidence of slowing of the functional declineClifford W Shults, David Oakes, Karl Kieburtz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2007
G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophyLaurie J Ozelius, Tatiana Foroud, Susanne May, et al.
Brain : a Journal of Neurology|April 1, 2025
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanismHolger Hengel, Shabab B Hannan, Selina Reich, et al.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome SequencingMirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Annals of Clinical and Translational Neurology|June 19, 2025
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome SequencingMirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 28, 2021
A Multi-center Genome-wide Association Study of Cervical DystoniaYan V Sun, Chengchen Li, Qin Hui, et al.
JAMA|September 14, 2021
Effect of Urate-Elevating Inosine on Early Parkinson Disease Progression: The SURE-PD3 Randomized Clinical Trial, Michael A Schwarzschild, Alberto Ascherio, et al.
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