Different saccadic abnormalities in PINK1 mutation carriers and in patients with non-genetic Parkinson's disease

J Neurol. 2009 Jul;256(7):1192-4. doi: 10.1007/s00415-009-5092-8. Epub 2009 Mar 29.
No abstract available

Publication types

  • Letter

MeSH terms

  • Aged
  • Basal Ganglia / physiopathology
  • Basal Ganglia Diseases / genetics
  • Basal Ganglia Diseases / physiopathology
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Eye Movements / genetics
  • Female
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genotype
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Neurologic Examination
  • Neuropsychological Tests
  • Ocular Motility Disorders / genetics*
  • Ocular Motility Disorders / physiopathology
  • Parkinson Disease / complications*
  • Parkinson Disease / genetics*
  • Parkinson Disease / physiopathology
  • Protein Kinases / genetics*
  • Psychomotor Performance / physiology
  • Saccades / genetics*

Substances

  • Genetic Markers
  • Protein Kinases
  • PTEN-induced putative kinase