Código QR (código de barras bidimensional)

Cognition and Evolution of Movement Disorders of FOXG1-Related Syndrome

FOXG1-related syndrome is a rare neurodevelopmental encephalopathy characterized by early onset hyperkinetic movement disorders, absent language, autistic features, epilepsy, and severe cognitive impairment. However, detailed evaluation of cognition and evolution of movement disorders over time have...

ver descrição completa

Na minha lista:
Principais autores: Lee-Chin Wong, Yen-Tzu Wu, Chia-Jui Hsu, Wen-Chin Weng, Wen-Che Tsai, Wang-Tso Lee
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019-06-01
coleção:Frontiers in Neurology
Assuntos:
FOXG1
movement disorder
hyperkinetic
hypokinetic
evolution
cognition
Acesso em linha:https://www.frontiersin.org/article/10.3389/fneur.2019.00641/full
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados