Neuropsychological stability over two years in asymptomatic carriers of the Huntington's disease mutation.
about
Suicidal ideation in Huntington disease: the role of comorbiditySelf-paced timing detects and tracks change in prodromal Huntington disease.Cognitive reserve and brain reserve in prodromal Huntington's disease.A novel cognitive-neurophysiological state biomarker in premanifest Huntington's disease validated on longitudinal data.Motor-Language Coupling in Huntington's Disease Families.Progression in prediagnostic Huntington disease.Seven-year clinical follow-up of premanifest carriers of Huntington's disease.Neuropsychological deficits in Huntington's disease gene carriers and correlates of early "conversion".Indexing disease progression at study entry with individuals at-risk for Huntington diseaseMovement sequencing in Huntington disease.Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review.Subtle changes among presymptomatic carriers of the Huntington's disease gene.Abnormal Electrophysiological Motor Responses in Huntington's Disease: Evidence of Premanifest Compensation.Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease.Functional compensation of motor function in pre-symptomatic Huntington's disease.Cognitive decline in prodromal Huntington Disease: implications for clinical trials.The most appropriate primary outcomes to design clinical trials on Huntington's disease: meta-analyses of cohort studies and randomized placebo-controlled trials.Stem cell therapy and cellular engineering for treatment of neuronal dysfunction in Huntington's disease.Brain activation and functional connectivity in premanifest Huntington's disease during states of intrinsic and phasic alertness.Temporal order memory deficits prior to clinical diagnosis in Huntington's disease.Longitudinal pilot-study of Sustained Attention to Response Task and P300 in manifest and pre-manifest Huntington's disease.A double blind evaluation of cognitive decline in a Norwegian cohort of asymptomatic carriers of Huntington's disease.Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease.Attention, inhibition, and proximity to clinical onset in preclinical mutation carriers for Huntington's disease.Longitudinal study evaluating neuropsychological changes in so-called asymptomatic carriers of the Huntington's disease mutation after 1 year.
P2860
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P2860
Neuropsychological stability over two years in asymptomatic carriers of the Huntington's disease mutation.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Neuropsychological stability o ...... Huntington's disease mutation.
@en
type
label
Neuropsychological stability o ...... Huntington's disease mutation.
@en
prefLabel
Neuropsychological stability o ...... Huntington's disease mutation.
@en
P2093
P2860
P356
P1476
Neuropsychological stability o ...... Huntington's disease mutation.
@en
P2093
A M Codori
J R Campodonico
P2860
P304
P356
10.1136/JNNP.61.6.621
P407
P577
1996-12-01T00:00:00Z