Spastin in the human and mouse central nervous system with special reference to its expression in the hippocampus of mouse pilocarpine model of status epilepticus and temporal lobe epilepsy

This publication has 31 references indexed in Scilit:

• Glutamate receptor 1-immunopositive neurons in the gliotic CA1 area of the mouse hippocampus after pilocarpine-induced status epilepticus
  European Journal of Neuroscience, 2005
• Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation
  European Journal of Neurology, 2004
• Identification of nuclear localisation sequences in spastin (SPG4) using a novel Tetra-GFP reporter system
  Biochemical and Biophysical Research Communications, 2004
• Expression of different isoforms of protein kinase C in the rat hippocampus after pilocarpine‐induced status epilepticus with special reference to CA1 area and the dentate gyrus
  Hippocampus, 2003
• Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus
  Human Molecular Genetics, 2003
• Hereditary spastic paraplegia: The pace quickens
  Annals of Neurology, 2002
• A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members
  Journal of Neurology, Neurosurgery & Psychiatry, 2001
• Hereditary spastic paraplegia associated with epilepsy, mental retardation and hearing impairment
  Spinal Cord, 1993
• Hereditary spastic paraplegia with epileptic myoclonus
  Acta Neurologica Scandinavica, 1991
• Hereditary spastic paraplegia in Western Norway
  Clinical Genetics, 1974