Clinical presentation and progression of sporadic and familial primary torsion dystonia in Italy

Adv Neurol. 2004:94:171-8.
No abstract available

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Age of Onset*
  • Aged
  • Aging
  • Carrier Proteins / genetics*
  • DNA Mutational Analysis
  • Disease Progression
  • Dystonia Musculorum Deformans / classification
  • Dystonia Musculorum Deformans / epidemiology*
  • Dystonia Musculorum Deformans / genetics
  • Dystonia Musculorum Deformans / physiopathology
  • Dystonic Disorders / classification
  • Dystonic Disorders / epidemiology*
  • Dystonic Disorders / genetics
  • Dystonic Disorders / physiopathology
  • Female
  • Genetic Testing / methods
  • Humans
  • Italy / epidemiology
  • Male
  • Middle Aged
  • Molecular Chaperones*
  • Mutation
  • Neurologic Examination / methods
  • Pedigree
  • Phenotype

Substances

  • Carrier Proteins
  • Molecular Chaperones
  • TOR1A protein, human