Identification of a Novel Non-Canonical Splice-Site Variant in ABCD1

por Zheng, Feixia, Lin, Zhongdong, Hu, Ying, Shi, Xulai, Zhao, Qianlei, Lin, Zhenlang
Publicado 2023

Basal ganglia calcification and novel compound heterozygous mutations in the PANK2 gene in a Chinese boy with classic Pantothenate kinase-associated neurodegeneration: A case repor...

por Shi, Xulai, Zheng, Feixia, Ye, Xiuyun, Li, Xiucui, Zhao, Qianlei, Lin, Zhongdong, Hu, Ying, Wang, Jiwen
Publicado 2018

Different experiences of two PRRT2-associated self-limited familial infantile epilepsy

por Zhao, Qianlei, Liu, Zhenwei, Hu, Ying, Fang, Shiyu, Zheng, Feixia, Li, Xiucui, Li, Feng, Lin, Zhongdong
Publicado 2020

Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia

por Li, Xiucui, Bao, Shijia, Wang, Wei, Shi, Xulai, Hu, Ying, Li, Feng, Zhao, Qianlei, Zheng, Feixia, Lin, Zhongdong
Publicado 2021

Myricetin attenuates hypoxic-ischemic brain damage in neonatal rats via NRF2 signaling pathway

por Chen, Tingting, Hu, Yingying, Lu, Liying, Zhao, Qianlei, Tao, Xiaoyue, Ding, Bingqing, Chen, Shangqin, Zhu, Jianghu, Guo, Xiaoling, Lin, Zhenlang
Publicado 2023

Meta-Analysis of Low Density Lipoprotein Receptor (LDLR) rs2228671 Polymorphism and Coronary Heart Disease

por Ye, Huadan, Zhao, Qianlei, Huang, Yi, Wang, Lingyan, Liu, Haibo, Wang, Chunming, Dai, Dongjun, Xu, Leiting, Ye, Meng, Duan, Shiwei
Publicado 2014