Striatal volume contributes to the prediction of onset of Huntington disease in incident cases.
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Correlations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/2 mouse model of HDCorrelations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/1 mouse model of Huntington's diseaseA two years longitudinal study of a transgenic Huntington disease monkey.Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational studyDynamics of the connectome in Huntington's disease: A longitudinal diffusion MRI study.T1ρ imaging in premanifest Huntington disease reveals changes associated with disease progression.In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.Executive functions in premanifest Huntington's disease.Stable Atlas-based Mapped Prior (STAMP) machine-learning segmentation for multicenter large-scale MRI data.Hippocampal and left subcallosal anterior cingulate atrophy in psychotic depressionAdult neurogenesis in humans- common and unique traits in mammals.The power-proportion method for intracranial volume correction in volumetric imaging analysisProgressive cognitive deficit, motor impairment and striatal pathology in a transgenic Huntington disease monkey model from infancy to adulthood.In Vivo MRI Evidence that Neuropathology is Attenuated by Cognitive Enrichment in the Yac128 Huntington's Disease Mouse Model.Abnormal Electrophysiological Motor Responses in Huntington's Disease: Evidence of Premanifest Compensation.Spatiotemporal mapping of brain atrophy in mouse models of Huntington's disease using longitudinal in vivo magnetic resonance imaging.Intra-individual Variability in Prodromal Huntington Disease and Its Relationship to Genetic BurdenIs There an Association of Physical Activity with Brain Volume, Behavior, and Day-to-day Functioning? A Cross Sectional Design in Prodromal and Early Huntington Disease.Frontolimbic neural circuitry at 6 months predicts individual differences in joint attention at 9 monthsLinking white matter and deep gray matter alterations in premanifest Huntington diseaseNetwork localization of hemichorea-hemiballismusNetwork topology and functional connectivity disturbances precede the onset of Huntington's disease.Striatal morphology correlates with frontostriatal electrophysiological motor processing in Huntington's disease: an IMAGE-HD study.Neuroimaging of rapidly progressive dementias, part 1: neurodegenerative etiologies.The cognitive burden in Huntington's disease: pathology, phenotype, and mechanisms of compensation.The Complexity of Clinical Huntington's Disease: Developments in Molecular Genetics, Neuropathology and Neuroimaging Biomarkers.Determinants of Onset of Huntington's Disease with Behavioral Symptoms: Insight from 92 Patients.Mapping the order and pattern of brain structural MRI changes using change-point analysis in premanifest Huntington's disease.Cognitive Control, Learning, and Clinical Motor Ratings Are Most Highly Associated with Basal Ganglia Brain Volumes in the Premanifest Huntington's Disease Phenotype.Cholinergic interneurons in the Q140 knockin mouse model of Huntington's disease: Reductions in dendritic branching and thalamostriatal input.Microstructural brain abnormalities in Huntington's disease: A two-year follow-up.Longitudinal diffusion changes in prodromal and early HD: Evidence of white-matter tract deterioration.Longitudinal resting state fMRI analysis in healthy controls and premanifest Huntington's disease gene carriers: a three-year follow-up study.Early and progressive circadian abnormalities in Huntington's disease sheep are unmasked by social environment.Surface-based morphometry reveals caudate subnuclear structural damage in patients with premotor Huntington disease.The Corticospinal Tract in Huntington's Disease.The role of iron in gray matter degeneration in Huntington's disease: a magnetic resonance imaging study.Diagnostic criteria for Huntington's disease based on natural history.Resting-state connectivity and modulated somatomotor and default-mode networks in Huntington disease.Resting-state functional MRI reveals altered brain connectivity and its correlation with motor dysfunction in a mouse model of Huntington's disease.
P2860
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P2860
Striatal volume contributes to the prediction of onset of Huntington disease in incident cases.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Striatal volume contributes to ...... ton disease in incident cases.
@ast
Striatal volume contributes to ...... ton disease in incident cases.
@en
type
label
Striatal volume contributes to ...... ton disease in incident cases.
@ast
Striatal volume contributes to ...... ton disease in incident cases.
@en
prefLabel
Striatal volume contributes to ...... ton disease in incident cases.
@ast
Striatal volume contributes to ...... ton disease in incident cases.
@en
P2093
P2860
P50
P1476
Striatal volume contributes to ...... ton disease in incident cases.
@en
P2093
Elizabeth H Aylward
James A Mills
PREDICT-HD Investigators and Coordinators of the Huntington Study Group
Ronald K Pierson
P2860
P304
P356
10.1016/J.BIOPSYCH.2011.07.030
P407
P577
2011-09-09T00:00:00Z