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Neuropsychological Deficits in Huntington’s Disease Gene Carriers and Correlates of Early “Conversion”

The authors examined whether the baseline cognitive functioning of 21 clinically normal huntingtin mutation carriers who developed manifest Huntington’s disease on follow-up differed from that of 49 mutation carriers who remain asymptomatic over the same period in a longitudinal study. One hundred t...

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Detalhes bibliográficos
Main Authors: Brandt, Jason, Inscore, Anjeli B., Ward, Julianna, Shpritz, Barnett, Rosenblatt, Adam, Margolis, Russell L., Ross, Christopher A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2966303/
https://ncbi.nlm.nih.gov/pubmed/19196932
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1176/appi.neuropsych.20.4.466
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