Tracking motor impairments in the progression of Huntington's disease. - Wikidata - awgldk - TriplyDB

Tracking motor impairments in the progression of Huntington's disease.

Tracking motor impairments in the progression of Huntington's disease.

http://www.wikidata.org/entity/Q34449476

about

Multivariate clustering of progression profiles reveals different depression patterns in prodromal Huntington disease.Statistical Approaches to Longitudinal Data Analysis in Neurodegenerative Diseases: Huntington's Disease as a Model.Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational study Longitudinal beta-binomial modeling using GEE for overdispersed binomial data.Dynamic Prediction of Motor Diagnosis in Huntington's Disease Using a Joint Modeling Approach.Functional connectivity of primary motor cortex is dependent on genetic burden in prodromal Huntington disease.Onset of Huntington's disease: can it be purely cognitive?Monoamine reuptake inhibitors in Parkinson's disease.Intra-individual Variability in Prodromal Huntington Disease and Its Relationship to Genetic Burden Assessing Decline: Visualising Progression in Huntington's Disease using a Clinical Dashboard with Enroll-HD Data.A Machine Learning Framework for Gait Classification Using Inertial Sensors: Application to Elderly, Post-Stroke and Huntington's Disease Patients.Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HD Advances in clinical trials for movement disorders.Validation of a prognostic index for Huntington's disease.Identification of extreme motor phenotypes in Huntington's disease.Does Vitamin C Influence Neurodegenerative Diseases and Psychiatric Disorders?The impact of oculomotor functioning on neuropsychological performance in Huntington disease.Patient-reported outcomes in Huntington's disease: Quality of life in neurological disorders (Neuro-QoL) and Huntington's disease health-related quality of life (HDQLIFE) physical function measures.Reliability and Validity of the HD-PRO-TriadTM, a Health-Related Quality of Life Measure Designed to Assess the Symptom Triad of Huntington's Disease.Safety and Exploratory Efficacy at 36 Months in Open-HART, an Open-Label Extension Study of Pridopidine in Huntington's Disease.Baseline multimodal information predicts future motor impairment in premanifest Huntington's disease.Gradient Boosted Trees for Corrective Learning

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P2860

Tracking motor impairments in the progression of Huntington's disease.

http://www.wikidata.org/entity/Q34449476

description

2013 nî lūn-bûn

@nan

2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Tracking motor impairments in the progression of Huntington's disease.

@ast

Tracking motor impairments in the progression of Huntington's disease.

@en

Tracking motor impairments in the progression of Huntington's disease.

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type

label

Tracking motor impairments in the progression of Huntington's disease.

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Tracking motor impairments in the progression of Huntington's disease.

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Tracking motor impairments in the progression of Huntington's disease.

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Tracking motor impairments in the progression of Huntington's disease.

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Tracking motor impairments in the progression of Huntington's disease.

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Tracking motor impairments in the progression of Huntington's disease.

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P1433

Movement Disorders

P1476

Tracking motor impairments in the progression of Huntington's disease.

@en

P2093

James A Mills

http://www.w3.org/2001/XMLSchema#string

Jeffery D Long

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Ji-In Kim

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Karen Marder

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Researchers of the PREDICT-HD Huntington's Study Group

http://www.w3.org/2001/XMLSchema#string

Ying Zhang

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P2860

An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriers

Evidence-based guideline: pharmacologic treatment of chorea in Huntington disease: report of the guideline development subcommittee of the American Academy of Neurology

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.

A joint model for nonlinear longitudinal data with informative dropout.

Estimating sample size for tests on trends across repeated measurements with missing data based on the interaction term in a mixed model.

Sample sizes for brain atrophy outcomes in trials for secondary progressive multiple sclerosis.

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.

Tapping linked to function and structure in premanifest and symptomatic Huntington disease

CAG-repeat length and the age of onset in Huntington disease (HD): a review and validation study of statistical approaches.

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scholarly article

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10.1002/MDS.25657

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3

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29

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Jane S. Paulsen

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2013-10-21T00:00:00Z

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260909823

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24150908

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Huntington disease

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