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Clinical Genetics|January 21, 2022
De novo variants in AGO1 recapitulate a heterogeneous neurodevelopmental disorder phenotypeYue Niu, Qiaoqiao Qian, Juan Li, et al.
Journal of Neurology|July 15, 2024
Clinical features and underlying etiology of children with Lennox-Gastaut syndromeZongpu Zhou, Xianru Jiao, Pan Gong, et al.
Developmental Medicine and Child Neurology|July 18, 2021
Phenotype of heterozygous variants of dehydrodolichol diphosphate synthaseXianru Jiao, Yinan Xue, Sai Yang, et al.
Neuroepidemiology|June 18, 2026
Health-Related Quality of Life and Family Impact Among Children with Epilepsy: The Role of Seizure ControlGenfu Zhang, Ang Ma, Zongpu Zhou, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 3, 2026
SCN1A-related epilepsy with spike-wave activation in sleep: A retrospective cohort and literature reviewAng Ma, Yue Niu, Zhao Xu, et al.
Pediatric Neurology|April 25, 2026
KCNA2 Variants in Epilepsy: Focusing on Spike-and-Wave Activation in SleepAng Ma, Pan Gong, Xianru Jiao, et al.
Journal of Medical Genetics|January 25, 2024
Genotype and phenotype correlation of PHACTR1-related neurological disordersZhao Xu, Lynette Sadleir, Himanshu Goel, et al.
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