Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging
- 20 October 2010
- journal article
- review article
- Published by Elsevier in Neurobiology of Disease
- Vol. 42 (2) , 202-209
- https://doi.org/10.1016/j.nbd.2010.10.010
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Increased sensorimotor network activity in DYT1 dystonia: a functional imaging studyBrain, 2010
- Primary dystonia: molecules and mechanismsNature Reviews Neurology, 2009
- Metabolic brain networks in neurodegenerative disorders: a functional imaging approachPublished by Elsevier ,2009
- Abnormal structure-function relationships in hereditary dystoniaNeuroscience, 2009
- The basal ganglia and cerebellum interact in the expression of dystonic movementBrain, 2008
- Modulation of metabolic brain networks after subthalamic gene therapy for Parkinson's diseaseProceedings of the National Academy of Sciences, 2007
- Sporadic adult onset dystonia: sensory abnormalities as an endophenotype in unaffected relativesJournal of Neurology, Neurosurgery & Psychiatry, 2007
- A Common Neural Network for Cognitive Reserve in Verbal and Object Working Memory in Young but not OldCerebral Cortex, 2007
- Intragenic Cis and Trans Modification of Genetic Susceptibility in DYT1 Torsion DystoniaAmerican Journal of Human Genetics, 2007
- The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinNature Genetics, 1997