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An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriersWHODAS 2.0 in prodromal Huntington disease: measures of functioning in neuropsychiatric diseasePerceived stress in prodromal Huntington disease.Indexing disease progression at study entry with individuals at-risk for Huntington diseaseThe role of the amygdala during emotional processing in Huntington's disease: from pre-manifest to late stage disease.Monitoring Huntington's disease progression through preclinical and early stagesCouples' coping in prodromal Huntington disease: a mixed methods study.Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HDCognitive impairment in Huntington disease: diagnosis and treatment.Cognitive decline in prodromal Huntington Disease: implications for clinical trials.Cognitive Control, Learning, and Clinical Motor Ratings Are Most Highly Associated with Basal Ganglia Brain Volumes in the Premanifest Huntington's Disease Phenotype.New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system).Neurodegenerative disease: Establishing a clinical trial battery for Huntington disease.Moving toward a gene therapy for Huntington's disease.The impact of oculomotor functioning on neuropsychological performance in Huntington disease.HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD).Factors related to genetic testing in adults at risk for Huntington disease: the prospective Huntington at-risk observational study (PHAROS).The Confluence of Psychiatric Symptoms and Neurodegenerative Disease: Impact on Genetic Counseling.Understanding the need for assistance with survey completion in people with Huntington disease.Evaluating cognition in individuals with Huntington disease: Neuro-QoL cognitive functioning measures.Whole-brain connectivity in a large study of Huntington's disease gene mutation carriers and healthy controls.Efficient ℓ0 -norm feature selection based on augmented and penalized minimization.Agreement between clinician-rated versus patient-reported outcomes in Huntington disease.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Early Detection of Huntington Disease.
@en
Early Detection of Huntington Disease.
@nl
type
label
Early Detection of Huntington Disease.
@en
Early Detection of Huntington Disease.
@nl
altLabel
Early detection of Huntington’s disease
@en
prefLabel
Early Detection of Huntington Disease.
@en
Early Detection of Huntington Disease.
@nl
P2860
P356
P1433
P1476
Early Detection of Huntington Disease.
@en
P2860
P304
P356
10.2217/FNL.09.78
P577
2010-01-01T00:00:00Z