Julie C. Stout

Monash University, Caulfield East, Victoria, Australia 
striatal-frontal systems, Huntington's Disease
"Julie Stout"
Mean distance: 14.6 (cluster 15)
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Reilmann R, Anderson KE, Feigin A, et al. (2024) Safety and efficacy of laquinimod for Huntington's disease (LEGATO-HD): a multicentre, randomised, double-blind, placebo-controlled, phase 2 study. The Lancet. Neurology
Atkins KJ, Andrews SC, Stout JC, et al. (2024) The effect of Huntington's disease on cognitive and physical motivation. Brain : a Journal of Neurology
Chan JCS, Stout JC, Shirbin CA, et al. (2021) Listener Detection of Objectively Validated Acoustic Features of Speech in Huntington's Disease. Journal of Huntington's Disease
Abreu D, Ware J, Georgiou-Karistianis N, et al. (2021) Utility of Huntington's Disease Assessments by Disease Stage: Floor/Ceiling Effects. Frontiers in Neurology. 12: 595679
Wasser CI, Mercieca EC, Kong G, et al. (2020) Gut dysbiosis in Huntington's disease: associations among gut microbiota, cognitive performance and clinical outcomes. Brain Communications. 2: fcaa110
McLaren B, Andrews SC, Glikmann-Johnston Y, et al. (2020) Feasibility and initial validation of 'HD-Mobile', a smartphone application for remote self-administration of performance-based cognitive measures in Huntington's disease. Journal of Neurology
Andrews SC, Langbehn DR, Craufurd D, et al. (2020) Apathy predicts rate of cognitive decline over 24 months in premanifest Huntington's disease. Psychological Medicine. 1-7
Carlozzi NE, Schilling SG, Boileau NR, et al. (2019) How different aspects of motor dysfunction influence day-to-day function in huntington's disease. Movement Disorders : Official Journal of the Movement Disorder Society
Ross CA, Reilmann R, Cardoso F, et al. (2019) Movement Disorder Society Task Force Viewpoint: Huntington's Disease Diagnostic Categories. Movement Disorders Clinical Practice. 6: 541-546
Carmichael AM, Irish M, Glikmann-Johnston Y, et al. (2019) Discrete changes in the frequency and functions of autobiographical reminiscence in Huntington's disease. Memory (Hove, England). 1-7
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