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Early changes in the hypothalamic region in prodromal Huntington disease revealed by MRI analysis
Huntington disease (HD) is a fatal neurodegenerative disorder caused by an expanded CAG repeat. Its length can be used to estimate the time of clinical diagnosis, which is defined by overt motor symptoms. Non-motor symptoms begin before motor onset, and involve changes in hypothalamus-regulated func...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2955781/ https://ncbi.nlm.nih.gov/pubmed/20682340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2010.07.013 |
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