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Movement Disorders : Official Journal of the Movement Disorder Society|February 15, 2024
Digital Measures of Postural Sway Quantify Balance Deficits in Spinocerebellar AtaxiaVrutangkumar V Shah, Daniel Muzyka, Adam Jagodinsky, et al.
The Lancet. Neurology|February 11, 2014
Efficacy and safety of rifampicin for multiple system atrophy: a randomised, double-blind, placebo-controlled trialPhillip A Low, David Robertson, Sid Gilman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 15, 2012
Common data elements for clinical research in Friedreich's ataxiaDavid R Lynch, Massimo Pandolfo, Jorg B Schulz, et al.
Movement Disorders Clinical Practice|December 18, 2025
Digital Gait Measures Discriminate People with Friedreich's Ataxia from Healthy ControlsHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2024
Standing Balance Conditions and Digital Sway Measures for Clinical Trials of Friedreich's AtaxiaHannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Cerebellum (London, England)|January 14, 2023
Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific GenotypesPilar Garces, Chrystalina A Antoniades, Anna Sobanska, et al.
Cerebellum (London, England)|April 28, 2023
Quantitative Oculomotor Assessment in Hereditary Ataxia: Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital-motor BiomarkersPilar Garces, Chrystalina A Antoniades, Anna Sobanska, et al.
American Journal of Medical Genetics. Part A|November 12, 2019
Healthcare recommendations for Joubert syndromeRuxandra Bachmann-Gagescu, Jennifer C Dempsey, Sara Bulgheroni, et al.
European Journal of Human Genetics : EJHG|March 3, 2016
Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome)Alessia Micalizzi, Andrea Poretti, Marta Romani, et al.
Annals of Neurology|February 3, 2006
AHI1 gene mutations cause specific forms of Joubert syndrome-related disordersEnza Maria Valente, Francesco Brancati, Jennifer L Silhavy, et al.
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