Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis

This publication has 112 references indexed in Scilit:

• TorsinA participates in endoplasmic reticulum-associated degradation
  Nature Communications, 2011
• The neural substrates of rapid-onset Dystonia-Parkinsonism
  Nature Neuroscience, 2011
• Molecular pathways in dystonia
  Neurobiology of Disease, 2010
• Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
  The Lancet Neurology, 2010
• CSN complex controls the stability of selected synaptic proteins via a torsinA-dependent process
  The EMBO Journal, 2010
• Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging
  Neurobiology of Disease, 2010
• Direct interaction between causative genes of DYT1 and DYT6 primary dystonia
  Annals of Neurology, 2010
• Neurophysiology of dystonia: The role of inhibition
  Neurobiology of Disease, 2010
• Increased sensorimotor network activity in DYT1 dystonia: a functional imaging study
  Brain, 2010
• The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
  Nature Genetics, 1997