Striatal volume contributes to the prediction of onset of Huntington disease in incident cases. - Wikidata - awgldk - TriplyDB

Striatal volume contributes to the prediction of onset of Huntington disease in incident cases.

Striatal volume contributes to the prediction of onset of Huntington disease in incident cases.

http://www.wikidata.org/entity/Q35612769

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Correlations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/2 mouse model of HD Correlations of behavioral deficits with brain pathology assessed through longitudinal MRI and histopathology in the R6/1 mouse model of Huntington's disease A two years longitudinal study of a transgenic Huntington disease monkey.Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational study Dynamics 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 depression Adult neurogenesis in humans- common and unique traits in mammals.The power-proportion method for intracranial volume correction in volumetric imaging analysis Progressive 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 Burden Is 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 months Linking white matter and deep gray matter alterations in premanifest Huntington disease Network localization of hemichorea-hemiballismus Network 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.

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Striatal volume contributes to the prediction of onset of Huntington disease in incident cases.

http://www.wikidata.org/entity/Q35612769

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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Striatal volume contributes to ...... ton disease in incident cases.

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Striatal volume contributes to ...... ton disease in incident cases.

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Striatal volume contributes to ...... ton disease in incident cases.

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J.BIOPSYCH.2011.07.030

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Biological Psychiatry

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Striatal volume contributes to ...... ton disease in incident cases.

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Dawei Liu

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Elizabeth H Aylward

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James A Mills

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PREDICT-HD Investigators and Coordinators of the Huntington Study Group

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Ronald K Pierson

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P2860

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

Longitudinal change in regional brain volumes in prodromal Huntington disease

Neuropsychological and neuroradiological correlates in Huntington's disease.

Huntington's disease: from molecular pathogenesis to clinical treatment.

Striatal and white matter predictors of estimated diagnosis for Huntington disease

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

Trinucleotide repeat length instability and age of onset in Huntington's disease.

Thalamic metabolism and symptom onset in preclinical Huntington's disease.

The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size

Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease.

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10.1016/J.BIOPSYCH.2011.07.030

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9

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71

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Jane S. Paulsen

Peggy C Nopoulos

Christopher A Ross

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2011-09-09T00:00:00Z

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51638802

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21907324

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corpus striatum

Huntington disease

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3237730

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