Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
about
Oromandibular dyskinesia as the initial manifestation of late-onset huntington diseaseDifferential vulnerability of neurons in Huntington's disease: the role of cell type-specific features.Tapping linked to function and structure in premanifest and symptomatic Huntington diseaseQuantitative assessment of motor abnormalities in untreated patients with major depressive disorderCoordination of fingertip forces during precision grip in premanifest Huntington's diseaseA retrospective analysis of hand tapping as a longitudinal marker of disease progression in Huntington's disease.Effect of tetrabenazine on motor function in patients with huntington disease.Quantitative motor assessment of muscular weakness in myasthenia gravis: a pilot study.Effects of focal hand dystonia on visually guided and internally guided force control.Grasping multiple sclerosis: do quantitative motor assessments provide a link between structure and function?Basal ganglia mechanisms underlying precision grip force controlThe most appropriate primary outcomes to design clinical trials on Huntington's disease: meta-analyses of cohort studies and randomized placebo-controlled trials.Wearable Sensors in Huntington Disease: A Pilot Study.Grasping premanifest Huntington's disease - shaping new endpoints for new trials.An Automated Home-Cage System to Assess Learning and Performance of a Skilled Motor Task in a Mouse Model of Huntington's DiseaseImpaired postural stability as a marker of premanifest Huntington's disease.Hand tapping: a simple, reproducible, objective marker of motor dysfunction in Huntington's disease.Use of hand-held dynamometry in the evaluation of lower limb muscle strength in people with Huntington's disease.Objective assessment of motor slowness in Huntington's disease: clinical correlates and 2-year follow-up.The pridopidine paradox in Huntington's disease.Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease.Assessment of involuntary choreatic movements in Huntington's disease--toward objective and quantitative measures.Depressed Synaptic Transmission and Reduced Vesicle Release Sites in Huntington's Disease Neuromuscular Junctions.Huntington's disease: objective assessment of posture--a link between motor and functional deficits.Quantitative motor assessment of dyskinesias in Parkinson's disease.
P2860
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P2860
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
@zh-my
2001年学术文章
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2001年學術文章
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2001年學術文章
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2001年學術文章
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name
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@en
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@nl
type
label
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@en
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@nl
prefLabel
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@en
Objective assessment of progression in Huntington's disease: a 3-year follow-up study.
@nl
P2093
P356
P1433
P1476
Objective assessment of progression in Huntington's disease: a 3-year follow-up study
@en
P2093
A M Gordon
H Henningsen
P304
P356
10.1212/WNL.57.5.920
P407
P577
2001-09-01T00:00:00Z