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Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia
OBJECTIVE: To determine whether changes in D(2) receptor availability are present in carriers of genetic mutations for primary dystonia. METHODS: Manifesting and nonmanifesting carriers of the DYT1 and DYT6 dystonia mutations were scanned with [(11)C] raclopride (RAC) and PET. Measures of D(2) recep...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Academy of Neurology
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2697963/ https://ncbi.nlm.nih.gov/pubmed/19528516 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181aa538f |
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