Classification and genetics of dystonia

This publication has 122 references indexed in Scilit:

• The parkin gene and its phenotype
  Neurological Sciences, 2001
• Cerebrospinal fluid homovanillic acid levels in rapid‐onset dystonia‐parkinsonism
  Annals of Neurology, 1998
• The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
  Nature Genetics, 1997
• Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p
  Annals of Neurology, 1997
• Mutations in the GTP cyclohydrolase I and 6-pyruvoyl-tetrahydropterin synthase genes
  Human Mutation, 1997
• Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation
  Annals of Neurology, 1994
• Dopa-responsive dystonia simulating cerebral palsy
  Pediatric Neurology, 1994
• Biochemical and fluorodopa positron emission tomographic findings in an asymptomatic carrier of the gene for dopa‐responsive dystonia
  Annals of Neurology, 1994
• Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34
  Annals of Neurology, 1990
• Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritance
  Annals of Neurology, 1989