Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

por Hu, Wenjing, Wang, Enhui, Fang, Hongjun, Li, Li, Yi, Jurong, Liu, Qingqing, Qing, Wei, Guo, Danni, Tan, Qianqian, Liao, Hongmei
Publicado 2023

Nabais Sa‐de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report

por Hu, Wenjing, Fang, Hongjun, Peng, Yu, Li, Li, Liu, Shulei, Liao, Hongmei, Tang, Jingwen, Yi, Jurong, Liu, Qingqing, Xu, Li, Wu, Liwen
Publicado 2022

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