Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease. - Wikidata - awgldk - TriplyDB

Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

http://www.wikidata.org/entity/Q45289317

about

Physiotherapy clinical guidelines for Huntington’s disease Force-plate quantification of progressive behavioral deficits in the R6/2 mouse model of Huntington's disease.Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data.A small molecule p75NTR ligand normalizes signalling and reduces Huntington's disease phenotypes in R6/2 and BACHD mice.Longitudinal Change in Gait and Motor Function in Pre-manifest Huntington's Disease.Deficits in stepping response time are associated with impairments in balance and mobility in people with Huntington disease.Variability in interval production is due to timing-dependent deficits in Huntington's disease.Gait in Huntington's disease and the stride length-cadence relationship Differential loss of thalamostriatal and corticostriatal input to striatal projection neuron types prior to overt motor symptoms in the Q140 knock-in mouse model of Huntington's disease.Understanding the Outcomes Measures used in Huntington Disease Pharmacological Trials: A Systematic Review.Tapping linked to function and structure in premanifest and symptomatic Huntington disease Clinimetric properties of the Tinetti Mobility Test, Four Square Step Test, Activities-specific Balance Confidence Scale, and spatiotemporal gait measures in individuals with Huntington's disease Coordination of fingertip forces during precision grip in premanifest Huntington's disease Clinical assessment of mobility and balance impairments in pre-symptomatic Huntington's disease Monitoring Huntington's disease progression through preclinical and early stages Quantitative gait analysis in essential tremor reveals impairments that are maintained into advanced age Timing control of gait: a study of essential tremor patients vs. age-matched controls A Longitudinal Motor Characterisation of the HdhQ111 Mouse Model of Huntington's Disease Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice.Learning fast accurate movements requires intact frontostriatal circuits.Early Detection of Huntington Disease.Discrete gait characteristics are associated with m.3243A>G and m.8344A>G variants of mitochondrial disease and its pathological consequences.Neurorehabilitation with neural transplantation.Moving forward on gait measurement: toward a more refined approach.Chorea associated with Huntington's disease: to treat or not to treat?Association between Various Brain Pathologies and Gait Disturbance.Development of a community-based exercise program for people diagnosed and at-risk for Huntington's disease: A clinical report.Wearable Sensors in Huntington Disease: A Pilot Study.Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy.Cholinergic interneurons in the Q140 knockin mouse model of Huntington's disease: Reductions in dendritic branching and thalamostriatal input.Fatigue leads to gait changes in spinal muscular atrophy.Quantitative Gait Analysis in Patients with Huntington's Disease Three-Dimensional Trunk and Lower Limbs Characteristics during Gait in Patients with Huntington's Disease.Video game play (Dance Dance Revolution) as a potential exercise therapy in Huntington's disease: a controlled clinical trial.Difficulty modifying a sustained motor response in prodromal Huntington's disease.Physical therapy in Huntington's disease--toward objective assessments?What effect does a structured home-based exercise programme have on people with Huntington's disease? A randomized, controlled pilot study.Selective subcortical contributions to gait impairments in males with the FMR1 premutation.Impairments in Spatiotemporal Gait Adaptation During Obstacle Navigation in Huntington's Disease.Disrupted striatal neuron inputs and outputs in Huntington's disease.

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P2860

Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

http://www.wikidata.org/entity/Q45289317

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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name

Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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type

label

Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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Movement Disorders

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Spectrum of gait impairments in presymptomatic and symptomatic Huntington's disease.

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P2093

Ashwini K Rao

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Carol B Moskowitz

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Karen S Marder

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Lisa Muratori

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P2860

Rate of functional decline in Huntington's disease. Huntington Study Group.

Predictors of nursing home placement in Huntington disease.

Huntington disease: clinical care and evaluation.

Huntington's disease: clinical correlates of disability and progression.

Motor changes in presymptomatic Huntington disease gene carriers.

Postural stability in patients with Huntington's disease.

The gait abnormality of Huntington's disease.

Evoked potentials in Huntington's disease. A comparative and longitudinal study.

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1100-1107

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10.1002/MDS.21987

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18412252

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Huntington disease