Abnormal structure-function relationships in hereditary dystonia.
about
From the genome to the phenome and back: linking genes with human brain function and structure using genetically informed neuroimagingIncreased sensorimotor network activity in DYT1 dystonia: a functional imaging study.Cerebellothalamocortical connectivity regulates penetrance in dystoniaCerebellar networks with the cerebral cortex and basal gangliaMeige syndrome: What's in a name?Contribution of TMS and rTMS in the Understanding of the Pathophysiology and in the Treatment of DystoniaEmerging concepts in the physiological basis of dystoniaNeural correlates of abnormal sensory discrimination in laryngeal dystonia.Increased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 DeltaGAG knock-in miceEarlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce.Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA.The subthalamic nucleus in primary dystonia: single-unit discharge characteristics.Abnormalities in metabolic network activity precede the onset of motor symptoms in Parkinson's disease.Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component.Functional brain networks and abnormal connectivity in the movement disorders.Impaired sequence learning in dystonia mutation carriers: a genotypic effect.PET Neuroimaging: Insights on Dystonia and Tourette Syndrome and Potential ApplicationsDirect interaction between causative genes of DYT1 and DYT6 primary dystonia.Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging.Genetic and clinical features of primary torsion dystonia.Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice.The cerebellum and basal ganglia are interconnectedThalamocortical Connectivity Correlates with Phenotypic Variability in DystoniaFunctional imaging in hereditary dystonia.The functional neuroanatomy of dystonia.Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.Neural expression of the transcription factor THAP1 during development in rat.Neural stem cell transplantation for the treatment of primary torsion dystonia: A case reportUnderstanding the anatomy of dystonia: determinants of penetrance and phenotype.Dystonia as a network disorder: what is the role of the cerebellum?Update on the pathology of dystonia.Milestones in neuroimaging.Milestones in dystonia.PET/CT in diagnosis of movement disorders.Primary dystonia: moribund or viable.Cerebellum: An explanation for dystonia?Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.Deep brain stimulation for dystonia: a novel perspective on the value of genetic testing.
P2860
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P2860
Abnormal structure-function relationships in hereditary dystonia.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
Abnormal structure-function relationships in hereditary dystonia.
@ast
Abnormal structure-function relationships in hereditary dystonia.
@en
type
label
Abnormal structure-function relationships in hereditary dystonia.
@ast
Abnormal structure-function relationships in hereditary dystonia.
@en
prefLabel
Abnormal structure-function relationships in hereditary dystonia.
@ast
Abnormal structure-function relationships in hereditary dystonia.
@en
P2860
P1433
P1476
Abnormal structure-function relationships in hereditary dystonia.
@en
P2093
P2860
P304
P356
10.1016/J.NEUROSCIENCE.2008.12.041
P407
P577
2009-01-01T00:00:00Z