Indexing disease progression at study entry with individuals at-risk for Huntington disease - Wikidata - awgldk - TriplyDB

Indexing disease progression at study entry with individuals at-risk for Huntington disease

Indexing disease progression at study entry with individuals at-risk for Huntington disease

http://www.wikidata.org/entity/Q35216637

about

Magnetic resonance imaging striatal volumes: a biomarker for clinical trials in Huntington's disease Huntington's disease cerebrospinal fluid seeds aggregation of mutant huntingtin.Multivariate clustering of progression profiles reveals different depression patterns in prodromal Huntington disease.Prefrontal cortex white matter tracts in prodromal Huntington disease Statistical Approaches to Longitudinal Data Analysis in Neurodegenerative Diseases: Huntington's Disease as a Model.Disruption of response inhibition circuits in prodromal Huntington disease.Cognitive reserve and brain reserve in prodromal Huntington's disease.Clinical and Biomarker Changes in Premanifest Huntington Disease Show Trial Feasibility: A Decade of the PREDICT-HD Study Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational study Regional atrophy associated with cognitive and motor function in prodromal Huntington disease.Neurochemical correlates of caudate atrophy in Huntington's disease.Longitudinal Psychiatric Symptoms in Prodromal Huntington's Disease: A Decade of Data.T1ρ imaging in premanifest Huntington disease reveals changes associated with disease progression.Longitudinal beta-binomial modeling using GEE for overdispersed binomial data.Executive functions in premanifest Huntington's disease.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.Targeted Local Support Vector Machine for Age-Dependent Classification.Regionally selective atrophy of subcortical structures in prodromal HD as revealed by statistical shape analysis.Onset of Huntington's disease: can it be purely cognitive?Tracking motor impairments in the progression of Huntington's disease.Everyday cognition in prodromal Huntington disease WHODAS 2.0 in prodromal Huntington disease: measures of functioning in neuropsychiatric disease Movement sequencing in Huntington disease.Analysis of longitudinal censored semicontinuous data with application to the study of executive dysfunction: The Towers Task.Quantitative 7T phase imaging in premanifest Huntington disease.Ubiquitin: a potential cerebrospinal fluid progression marker in Huntington's disease.Novel Nut and Bolt Task Quantifies Motor Deficits in Premanifest and Manifest Huntington's Disease FUSED KERNEL-SPLINE SMOOTHING FOR REPEATEDLY MEASURED OUTCOMES IN A GENERALIZED PARTIALLY LINEAR MODEL WITH FUNCTIONAL SINGLE INDEX.Intra-individual Variability in Prodromal Huntington Disease and Its Relationship to Genetic Burden Performance of the 12-item WHODAS 2.0 in prodromal Huntington disease.Development of the Huntington disease work function scale Measuring executive dysfunction longitudinally and in relation to genetic burden, brain volumetrics, and depression in prodromal Huntington disease Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HD Linking white matter and deep gray matter alterations in premanifest Huntington disease Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression.Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington Disease.Diffusion weighted imaging of prefrontal cortex in prodromal Huntington's disease.8OHdG as a marker for Huntington disease progression Modeling Variability in the Progression of Huntington's Disease A Novel Modeling Approach Applied to Structural Imaging Markers from TRACK-HD.

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Indexing disease progression at study entry with individuals at-risk for Huntington disease

http://www.wikidata.org/entity/Q35216637

description

2011 nî lūn-bûn

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2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

Indexing disease progression a ...... at-risk for Huntington disease

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P1433

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

P1476

Indexing disease progression a ...... at-risk for Huntington disease

@en

P2093

James A Mills

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

John H Warner

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PREDICT-HD Investigators and Coordinators of the Huntington Study Group

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Wenjing Lu

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Ying Zhang

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P2860

Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

Self-paced timing detects and tracks change in prodromal Huntington disease.

Longitudinal change in regional brain volumes in prodromal Huntington disease

Time-dependent ROC curves for censored survival data and a diagnostic marker.

Family and molecular data for a fine analysis of age at onset in Huntington disease.

Automatic detection of preclinical neurodegeneration: presymptomatic Huntington disease.

"Frontal" behaviors before the diagnosis of Huntington's disease and their relationship to markers of disease progression: evidence of early lack of awareness.

Striatal and white matter predictors of estimated diagnosis for Huntington disease

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751-763

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scholarly article

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10.1002/AJMG.B.31232

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7

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156B

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Jane S. Paulsen

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2011-08-19T00:00:00Z

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51587720

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21858921

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Huntington disease

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3174494

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