Odor identification in Huntington's disease patients and asymptomatic gene carriers

Frederick W. Bylsma, Paul J. Moberg, Richard L. Doty, Jason Brandt

Research output: Contribution to journalArticle

Abstract

Odor identification was assessed in 20 Huntington's disease (HD) patients, 20 normal adults with the genetic mutation that causes HD, and 20 mutation-negative adults. The University of Pennsylvania Smell Identification Test (UPSIT) revealed substantial odor identification deficits only in HD patients.

Original languageEnglish (US)
Pages (from-to)598-600
Number of pages3
JournalJournal of Neuropsychiatry and Clinical Neurosciences
Volume9
Issue number4
StatePublished - Sep 1997
Externally publishedYes

Fingerprint

Huntington Disease
Genes
Mutation
Smell
Odorants

ASJC Scopus subject areas

  • Neuropsychology and Physiological Psychology
  • Neuroscience(all)

Cite this

Odor identification in Huntington's disease patients and asymptomatic gene carriers. / Bylsma, Frederick W.; Moberg, Paul J.; Doty, Richard L.; Brandt, Jason.

In: Journal of Neuropsychiatry and Clinical Neurosciences, Vol. 9, No. 4, 09.1997, p. 598-600.

Research output: Contribution to journalArticle

Bylsma, Frederick W. ; Moberg, Paul J. ; Doty, Richard L. ; Brandt, Jason. / Odor identification in Huntington's disease patients and asymptomatic gene carriers. In: Journal of Neuropsychiatry and Clinical Neurosciences. 1997 ; Vol. 9, No. 4. pp. 598-600.
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