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Neurochemical correlates of caudate atrophy in Huntington disease
BACKGROUND: The precise pathogenic mechanisms of Huntington disease (HD) are unknown, but can be tested in vivo using proton magnetic resonance spectroscopy ((1)H MRS) to measure neurochemical changes. OBJECTIVE: To evaluate neurochemical differences in HD gene mutation-carriers (HGMC) vs. controls,...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3960319/ https://ncbi.nlm.nih.gov/pubmed/24442623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.25801 |
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