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Impaired intracortical inhibition demonstrated in vivo in people with Dravet syndrome
OBJECTIVE: Dravet syndrome is a rare neurodevelopmental disorder characterized by seizures and other neurologic problems. SCN1A mutations account for ∼80% of cases. Animal studies have implicated mutation-related dysregulated cortical inhibitory networks in its pathophysiology. We investigated such...
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| Publicat a: | Neurology |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5405762/ https://ncbi.nlm.nih.gov/pubmed/28356460 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003868 |
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