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The neural substrates of rapid-onset Dystonia-Parkinsonism.Genetic background modulates the phenotype of a mouse model of DYT1 dystoniaDevelopmental profile of the aberrant dopamine D2 receptor response in striatal cholinergic interneurons in DYT1 dystoniaTorsins: not your typical AAA+ ATPasesStriatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystoniaEvaluation of spontaneous propulsive movement as a screening tool to detect rescue of Parkinsonism phenotypes in zebrafish models.Objective Evaluation of Performance Stress in Musicians With Focal Hand Dystonia: A Case Series.TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegenerationA novel function for the Caenorhabditis elegans torsin OOC-5 in nucleoporin localization and nuclear importTiagabine treatment in kainic acid induced cerebellar lesion of dystonia rat model.In vivo imaging reveals impaired connectivity across cortical and subcortical networks in a mouse model of DYT1 dystonia.The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6).Interactions between nuclei and the cytoskeleton are mediated by SUN-KASH nuclear-envelope bridges.The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component.Current Gaps in the Understanding of the Subcellular Distribution of Exogenous and Endogenous Protein TorsinA.Inner nuclear membrane proteins: impact on human disease.PET Neuroimaging: Insights on Dystonia and Tourette Syndrome and Potential ApplicationsBasal ganglia contributions to motor control: a vigorous tutorThe external globus pallidus: progress and perspectivesHereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging.Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice.Increased volume and impaired function: the role of the basal ganglia in writer's cramp.Abnormal movement preparation in task-specific focal hand dystonia.Intracellular complexes of the early-onset torsion dystonia-associated AAA+ ATPase TorsinA.Basal Ganglia disorders associated with imbalances in the striatal striosome and matrix compartments.Inherited isolated dystonia: clinical genetics and gene function.A new treatment for focal dystonias: incobotulinumtoxinA (Xeomin®), a botulinum neurotoxin type A free from complexing proteinsReduced Number of Pigmented Neurons in the Substantia Nigra of Dystonia Patients? Findings from Extensive Neuropathologic, Immunohistochemistry, and Quantitative Analyses.Alternative approaches to modeling hereditary dystonias.Thalamocortical Connectivity Correlates with Phenotypic Variability in DystoniaMouse models of neurodevelopmental disease of the basal ganglia and associated circuits.Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1.Neuropathology of cervical dystonia.Nuclear positioning.Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia.Sonographic Alteration of Basal Ganglia in Different Forms of Primary Focal Dystonia: A Cross-sectional StudyCell Mechanosensitivity is Enabled by the LINC Nuclear Complex.Disruption of Protein Processing in the Endoplasmic Reticulum of DYT1 Knock-in Mice Implicates Novel Pathways in Dystonia Pathogenesis.Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia
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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 13 October 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Primary dystonia: molecules and mechanisms.
@en
Primary dystonia: molecules and mechanisms.
@nl
type
label
Primary dystonia: molecules and mechanisms.
@en
Primary dystonia: molecules and mechanisms.
@nl
prefLabel
Primary dystonia: molecules and mechanisms.
@en
Primary dystonia: molecules and mechanisms.
@nl
P2860
P1476
Primary dystonia: molecules and mechanisms
@en
P2093
Connie E Kim
Noga Alagem
P2860
P2888
P304
P356
10.1038/NRNEUROL.2009.160
P407
P577
2009-10-13T00:00:00Z