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Journal of Visualized Experiments : Jove|November 21, 2017
High-throughput Analysis of Locomotor Behavior in the Drosophila Island AssayIlse Eidhof, Michaela Fenckova, Dei M Elurbe, et al.Journal of Neurology|November 7, 2021
Pharmacological and non-pharmacological management of spinocerebellar ataxia: A systematic reviewKah Hui Yap, Shahrul Azmin, Jemaima Che Hamzah, et al.Journal of Parkinson'S Disease|July 12, 2020
Young Onset Parkinson's Disease: A Modern and Tailored ApproachBart Post, Lieneke van den Heuvel, Teije van Prooije, et al.Movement Disorders Clinical Practice|August 29, 2025
Botulinum Toxin Efficacy in Upper Limb Tremor: A Systematic Review and Meta-AnalysisIris M Visser, Yuvadee Pitakpatapee, Bart van de Warrenburg, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2020
Inclusion body myositis in patients with spinocerebellar ataxia types 3 and 6Anke Rietveld, Judith van Gaalen, Christiaan Saris, et al.European Journal of Medical Genetics|December 21, 2018
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxiaAakash Shetty, Ziv Gan-Or, Setareh Ashtiani, et al.Sensors (Basel, Switzerland)|July 29, 2023
Automated Gait Analysis Based on a Marker-Free Pose Estimation ModelChang Soon Tony Hii, Kok Beng Gan, Nasharuddin Zainal, et al.Annals of Neurology|October 24, 2017
A recessive ataxia diagnosis algorithm for the next generation sequencing eraMathilde Renaud, Christine Tranchant, Juan Vicente Torres Martin, et al.Journal of the Neurological Sciences|January 15, 2008
Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspotsChristian Beetz, Rebecca Schüle, Stephan Klebe, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 31, 2022
Digital Gait Biomarkers Allow to Capture 1-Year Longitudinal Change in Spinocerebellar Ataxia Type 3Winfried Ilg, Björn Müller, Jennifer Faber, et al.Pageof 6