Biblioteca Humberto Rosselli Quijano
Información del autor
Autor Mikaela A. Rowe |
Documentos disponibles escritos por este autor (1)
Refinar búsqueda
Visual evoked potential abnormalities in phelan-mcdermid syndrome / Paige M. Siper en Journal of the American Academy of Child & Adolescent Psychiatry, Año 2022 Vol. 61 - No. 4 (Abril)
[artículo]
Título : Visual evoked potential abnormalities in phelan-mcdermid syndrome Tipo de documento: texto impreso Autores: Paige M. Siper, Autor ; Mikaela A. Rowe, Autor ; Sylvia B. Guillory, Autor Fecha de publicación: 2022 Artículo en la página: pp. 565-574 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Síndrome de Phelan-McDermid, Trastorno del espectro autista, Potencial evocado visual, PEV transitorio Resumen: The current study used visual evoked potentials (VEPs) to examine excitatory and inhibitory postsynaptic activity in children with Phelan-McDermid syndrome (PMS) and the association with genetic factors. PMS is caused by haploinsufficiency of SHANK3 on chromosome 22 and represents a common single-gene cause of autism spectrum disorder (ASD) and intellectual disability. Link: ./index.php?lvl=notice_display&id=28421
in Journal of the American Academy of Child & Adolescent Psychiatry > Año 2022 Vol. 61 - No. 4 (Abril) . - pp. 565-574[artículo] Visual evoked potential abnormalities in phelan-mcdermid syndrome [texto impreso] / Paige M. Siper, Autor ; Mikaela A. Rowe, Autor ; Sylvia B. Guillory, Autor . - 2022 . - pp. 565-574.
Idioma : Inglés (eng) Idioma original : Inglés (eng)
in Journal of the American Academy of Child & Adolescent Psychiatry > Año 2022 Vol. 61 - No. 4 (Abril) . - pp. 565-574
Palabras clave: Síndrome de Phelan-McDermid, Trastorno del espectro autista, Potencial evocado visual, PEV transitorio Resumen: The current study used visual evoked potentials (VEPs) to examine excitatory and inhibitory postsynaptic activity in children with Phelan-McDermid syndrome (PMS) and the association with genetic factors. PMS is caused by haploinsufficiency of SHANK3 on chromosome 22 and represents a common single-gene cause of autism spectrum disorder (ASD) and intellectual disability. Link: ./index.php?lvl=notice_display&id=28421