Genotype–phenotype interactions in primary dystonias revealed by differential changes in brain structure
Open Access
- 1 April 2009
- journal article
- Published by Elsevier in NeuroImage
- Vol. 47 (4) , 1141-1147
- https://doi.org/10.1016/j.neuroimage.2009.03.057
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Glial elements contribute to stress-induced torsinA expression in the CNS and peripheral nervous systemNeuroscience, 2008
- A fast diffeomorphic image registration algorithmNeuroImage, 2007
- Bilateral grey-matter increase in the putamen in primary blepharospasmJournal of Neurology, Neurosurgery & Psychiatry, 2006
- Brainstem pathology in DYT1 primary torsion dystoniaAnnals of Neurology, 2004
- Microstructural white matter changes in carriers of the DYT1 gene mutationAnnals of Neurology, 2004
- Primary dystonia: Is abnormal functional brain architecture linked to genotype?Annals of Neurology, 2002
- Functional brain networks in DYT1 dystoniaAnnals of Neurology, 1998
- Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutationAnnals of Neurology, 1994
- Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritanceAnnals of Neurology, 1989
- Human gene for torsion dystonia located on chromosome 9q32-q34Neuron, 1989