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Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Neurology and Therapy|January 15, 2025
Content Validity of the Friedreich Ataxia Rating Scale in Patients with Spinocerebellar AtaxiaMichele Potashman, Katja Rudell, Naomi Suminski, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2022
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4Livia Parodi, Mathieu Barbier, Maxime Jacoupy, et al.
Brain : a Journal of Neurology|April 23, 2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxiaAdriana P Rebelo, Ilse Eidhof, Vivian P Cintra, et al.
Cerebellum (London, England)|November 28, 2023
Using Smartphone Sensors for Ataxia Trials: Consensus Guidance by the Ataxia Global Initiative Working Group on Digital-Motor BiomarkersAndrea H Németh, Chrystalina A Antoniades, Juergen Dukart, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Genome-wide association study confirms extant PD risk loci among the DutchJavier Simón-Sánchez, Jacobus J van Hilten, Bart van de Warrenburg, et al.
Research Square|November 28, 2023
Cerebellar volumetry in ataxias: Relation to ataxia severity and durationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
Cerebellum (London, England)|February 16, 2024
Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and DurationMónica Ferreira, Tamara Schaprian, David Kügler, et al.
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