Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

por Kang, Qingyun, Liao, Hongmei, Yang, Liming, Fang, Hongjun, Ning, Zeshu, Liao, Caishi, Gan, Siyi, Wu, Liwen
Publicado 2023

A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report

por Kang, Qingyun, Yang, Liming, Liao, Hongmei, Yang, Sai, Kuang, Xiaojun, Ning, Zeshu, Liao, Caishi, Chen, Bo
Publicado 2021

Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation

por Kang, Qingyun, Yang, Liming, Liao, Hongmei, Yang, Sai, Yang, Haiyang, Ning, Zeshu, Liao, Caishi, Wu, Liwen
Publicado 2021

Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

por Yang, Sai, Shen, Xiang, Kang, Qingyun, Kuang, Xiaojun, Ning, Zeshu, Liu, Shulei, Liao, Hongmei, Cao, Zhenhua, Yang, Liming
Publicado 2020

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations

por Hu, Wenjing, Fang, Hongjun, Peng, Yu, Li, Li, Guo, Danni, Tang, Jingwen, Yi, Jurong, Liu, Qingqing, Qin, Wei, Wu, Liwen, Ning, Zeshu
Publicado 2022

Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study

por Jiang, Zhi, Liao, Hongmei, Wu, Liwen, Hu, Wenjing, Yang, Liming, Chen, Bo, Ning, Zeshu, Tang, Jingwen, Xu, Rong, Chen, Mei, Guo, Feng, Liu, Shulei
Publicado 2023