Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis
- 31 December 2011
- journal article
- review article
- Published by Elsevier BV in The Lancet Neurology
- Vol. 10 (12), 1074-1085
- https://doi.org/10.1016/s1474-4422(11)70232-0
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- TorsinA participates in endoplasmic reticulum-associated degradationNature Communications, 2011
- Molecular pathways in dystoniaNeurobiology of Disease, 2011
- Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimagingNeurobiology of Disease, 2011
- Neurophysiology of dystonia: The role of inhibitionNeurobiology of Disease, 2011
- The neural substrates of rapid-onset Dystonia-ParkinsonismNature Neuroscience, 2011
- Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental studyThe Lancet Neurology, 2011
- CSN complex controls the stability of selected synaptic proteins via a torsinA-dependent processThe EMBO Journal, 2010
- Direct interaction between causative genes of DYT1 and DYT6 primary dystoniaAnnals of Neurology, 2010
- Increased sensorimotor network activity in DYT1 dystonia: a functional imaging studyBrain, 2010
- The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinNature Genetics, 1997