De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile Spasms

por Duan, Haolin, Peng, Jing, Kessi, Miriam, Yin, Fei
Publicado 2018

A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes

por Kessi, Miriam, Peng, Jing, Yang, Lifen, Duan, Haolin, Tang, Yulin, Yin, Fei
Publicado 2018

Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review

por Kessi, Miriam, Peng, Jing, Yang, Lifen, Xiong, Juan, Duan, Haolin, Pang, Nan, Yin, Fei
Publicado 2018

Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients

por Xiong, Juan, Duan, Haolin, Chen, Shimeng, Kessi, Miriam, He, Fang, Deng, Xiaolu, Zhang, Ciliu, Yang, Li, Peng, Jing, Yin, Fei
Publicado 2021

Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder

por Xiong, Juan, Liu, Zhonghua, Chen, Shimeng, Kessi, Miriam, Chen, Baiyu, Duan, Haolin, Deng, Xiaolu, Yang, Lifen, Peng, Jing, Yin, Fei
Publicado 2022

Attention-deficit/hyperactive disorder updates

por Kessi, Miriam, Duan, Haolin, Xiong, Juan, Chen, Baiyu, He, Fang, Yang, Lifen, Ma, Yanli, Bamgbade, Olumuyiwa A., Peng, Jing, Yin, Fei
Publicado 2022

Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy

por Kessi, Miriam, Xiong, Juan, Wu, Liwen, Yang, Lifen, He, Fang, Chen, Chen, Pang, Nan, Duan, Haolin, Zhang, Wen, Arafat, Ahmed, Yin, Fei, Peng, Jing
Publicado 2018

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review

por Kessi, Miriam, Peng, Jing, Duan, Haolin, He, Hailan, Chen, Baiyu, Xiong, Juan, Wang, Ying, Yang, Lifen, Wang, Guoli, Kiprotich, Karlmax, Bamgbade, Olumuyiwa A., He, Fang, Yin, Fei
Publicado 2022