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Dysarthria and broader motor speech deficits in Dravet syndrome

OBJECTIVE: To analyze the oral motor, speech, and language phenotype in 20 children and adults with Dravet syndrome (DS) associated with mutations in SCN1A. METHODS: Fifteen verbal and 5 minimally verbal DS patients with SCN1A mutations (aged 15 months-28 years) underwent a tailored assessment batte...

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Detalhes bibliográficos
Publicado no:Neurology
Main Authors: Turner, Samantha J., Brown, Amy, Arpone, Marta, Anderson, Vicki, Morgan, Angela T., Scheffer, Ingrid E.
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5344083/
https://ncbi.nlm.nih.gov/pubmed/28148630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003635
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