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Thalamic metabolism and symptom onset in preclinical Huntington’s disease

The neural basis for the transition from preclinical to symptomatic Huntington’s disease (HD) is unknown. We used serial positron emission tomography (PET) imaging in preclinical HD gene carriers (p-HD) to assess the metabolic changes that occur during this period. Twelve p-HD subjects were followed...

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Detalhes bibliográficos
Publicado no:Brain
Main Authors: Feigin, A., Tang, C., Ma, Y., Mattis, P., Zgaljardic, D., Guttman, M., Paulsen, J. S., Dhawan, V., Eidelberg, D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4455546/
https://ncbi.nlm.nih.gov/pubmed/17893097
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awm217
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