A term neonate with early myoclonic encephalopathy caused by RARS2 gene variants: a case report

por Xu, Yan, Wu, Bing-Bing, Wang, Hui-Jun, Zhou, Shui-Zhen, Cheng, Guo-Qiang, Zhou, Yuan-Feng
Publicado 2020

Early initial video-electro-encephalography combined with variant location predict prognosis of KCNQ2-related disorder

por Xu, Yan, Dou, Ya-lan, Chen, Xiang, Dong, Xin-ran, Wang, Xin-hua, Wu, Bing-bing, Cheng, Guo-qiang, Zhou, Yuan-feng
Publicado 2021

Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole‐exome sequencing

por Xu, Yan, Zhao, Rui, Wang, Min, Wang, Xin‐hua, Wang, Yi, Li, Hao, Ma, Yang‐yang, Wu, Bing‐bing, Zhou, Yuan‐feng
Publicado 2022

Associations Between High-Sensitivity C-Reactive Protein and All-Cause Mortality Among Oldest-Old in Chinese Longevity Areas: A Community-Based Cohort Study

por Chen, Pei-Liang, Li, Zhi-Hao, Yang, Hai-Lian, Cao, Zhao-Jin, Cheng, Xin, Zhao, Feng, Zhang, Xi-Ru, Lv, Yue-Bin, Li, Fu-Rong, Zhou, Yuan-Feng, Li, Hao-Nan, Qu, Ying-Li, Yin, Zhao-Xue, Liu, Ling, Wu, Xian-Bo, Shi, Xiao-Ming, Mao, Chen
Publicado 2022