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Frontiers in Molecular Neuroscience|June 6, 2022
<i>SHROOM4</i> Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized DischargesWen-Jun Bian, Zong-Jun Li, Jie Wang, et al.Journal of Neurodevelopmental Disorders|March 22, 2018
Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndromeNa He, Bing-Mei Li, Zhao-Xia Li, et al.Journal of Medical Genetics|July 4, 2024
<i>IFIH1</i> variants are associated with generalised epilepsy preceded by febrile seizuresWang Song, Wen-Jun Bian, Hua Li, et al.Seizure|May 7, 2019
Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlationZi-Rong Chen, De-Tian Liu, Heng Meng, et al.Molecular Neurobiology|March 13, 2016
A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic DrugQu-Wen Gao, Li-Dong Hua, Jie Wang, et al.Frontiers in Genetics|November 16, 2020
Heterozygous <i>PGM3</i> Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete PenetranceXiao-Rong Liu, Wen-Jun Bian, Jie Wang, et al.Epilepsy Research|October 24, 2022
BCOR variants are associated with X-linked recessive partial epilepsyXiang Li, Wen-Jun Bian, Xiao-Rong Liu, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 1, 2022
CELSR1 variants are associated with partial epilepsy of childhoodZheng Chen, Sheng Luo, Zhi-Gang Liu, et al.Frontiers in Molecular Neuroscience|May 23, 2022
<i>CACNA1A</i> Mutations Associated With Epilepsies and Their Molecular Sub-Regional ImplicationsXue-Lian Li, Zong-Jun Li, Xiao-Yu Liang, et al.Brain : a Journal of Neurology|April 20, 2021
UNC13B variants associated with partial epilepsy with favourable outcomeJie Wang, Jing-Da Qiao, Xiao-Rong Liu, et al.Pageof 2