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Reader Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington 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
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
Identification of symbol digit modality test score extremes in Huntington's disease
Cross-sectional and longitudinal voxel-based grey matter asymmetries in Huntington's disease
Interrater Reliability of the Unified Huntington's Disease Rating Scale-Total Motor Score Certification
Does arterial hypertension influence the onset of Huntington's disease?
Design Optimization for Clinical Trials in Early-Stage Manifest Huntington's Disease
Survival End Points for Huntington Disease Trials Prior to a Motor Diagnosis
Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease
Progression of motor subtypes in Huntington's disease: a 6-year follow-up study
A randomized, controlled trial of a multi-modal exercise intervention in Huntington's disease
Progression of motor subtypes in Huntington's disease: a 6-year follow-up study
The impact of occipital lobe cortical thickness on cognitive task performance: An investigation in Huntington's Disease
Force modulation deficits in complex regional pain syndrome: A potential role for impaired sense of force production
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
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
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