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(1 - 24 of 29)
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Apathy predicts rate of cognitive decline over 24 months in premanifest Huntington's disease
Association of CAG Repeats With Long-term Progression in Huntington Disease
Apathy Associated With Impaired Recognition of Happy Facial Expressions in Huntington's Disease
Apathy and atrophy of subcortical brain structures in Huntington's disease: A two-year follow-up study
Executive Impairment Is Associated With Unawareness of Neuropsychiatric Symptoms in Premanifest and Early Huntington's Disease
Development of Clinical Practice Guidelines for Management of Agitation, Anxiety, Apathy, Psychosis, and Sleep Disorders Associated with Huntington Disease
Progression of motor subtypes in Huntington's disease: a 6-year follow-up study
Development of Standard of Practice Guides for Treatment of Agitation, Anxiety, Apathy, Psychosis and Sleep Disorders in Huntington Disease
Progression of motor subtypes in Huntington's disease: a 6-year follow-up study
Reliability and Factor Structure of the Short Problem Behaviors Assessment for Huntington's Disease (PBA-s) in the TRACK-HD and REGISTRY studies
Protocol for the Development of Standard of Practice Guides for the Symptomatic Treatment of Huntington Disease
Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY)
DIFFUSION TENSOR IMAGING AND NEUROPSYCHIATRIC DISTURBANCE IN HUNTINGTON'S DISEASE
Suicidal ideation in a European Huntington's disease population
The structural correlates of functional deficits in early huntington's disease
Better global and cognitive functioning in choreatic versus hypokinetic-rigid Huntington's disease
Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data
The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients
Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy
Magnetization Transfer Imaging in Premanifest and Manifest Huntington Disease: A 2-Year Follow-Up
A Randomized, Double-blind, Placebo-Controlled Study of Latrepirdine in Patients With Mild to Moderate Huntington Disease
BETTER GLOBAL AND COGNITIVE FUNCTIONING FOR CHOREATIC COMPARED TO HYPOKINETIC-RIGID HUNTINGTON'S DISEASE
CORPUS CALLOSAL ATROPHY IN HUNTINGTON'S DISEASE
Magnetization Transfer Imaging in Premanifest and Manifest Huntington Disease: A 2-Year Follow-Up
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