Graphene Oxide-Polymer Composite Langmuir Films Constructed by Interfacial Thiol-Ene Photopolymerization

por Luo, Xiaona, Ma, Kai, Jiao, Tifeng, Xing, Ruirui, Zhang, Lexin, Zhou, Jingxin, Li, Bingbing
Publicado 2017

Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy

por Sun, Xiaoang, Luo, Xiaona, Lin, Longlong, Wang, Simei, Wang, Chunmei, Yuan, Fang, Lan, Xiaoping, Yan, Jingbin, Chen, Yucai
Publicado 2023

Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in China

por Sun, Xiaoang, Liu, Meiyan, Luo, Xiaona, Yuan, Fang, Wang, Chunmei, Wang, Simei, Xu, Quanmei, Zhang, Yuanfeng, Chen, Yucai
Publicado 2022

Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese Children

por Wang, Simei, Xu, Quanmei, Wang, Anqi, Yuan, Fang, Luo, Xiaona, Wang, Yilin, Guo, Miao, Zhang, Yuanfeng, Zhang, Wenjing, Ji, Xiaobing, Ren, Yun, Chen, Yucai
Publicado 2022

Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases

por Liu, Meiyan, Sun, Xiaoang, Lin, Longlong, Luo, Xiaona, Wang, Simei, Wang, Chunmei, Zhang, Yuanfeng, Xu, Quanmei, Xu, Wuhen, Wu, Shengnan, Lan, Xiaoping, Chen, Yucai
Publicado 2022

Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome

por Wang, Chunmei, Luo, Xiaona, Wang, Yilin, Liu, Zhao, Wu, Shengnan, Wang, Simei, Lan, Xiaoping, Xu, Quanmei, Xu, Wuhen, Yuan, Fang, Wang, Anqi, Zeng, Fanyi, Jia, Jia, Chen, Yucai
Publicado 2021

MED12-Related Disease in a Chinese Girl: Clinical Characteristics and Underlying Mechanism

por Wang, Chao, Lin, Longlong, Xue, Yan, Wang, Yilin, Liu, Zhao, Ou, Zicheng, Wu, Shengnan, Lan, Xiaoping, Zhang, Yuanfeng, Yuan, Fang, Luo, Xiaona, Wang, Chunmei, Xi, Jiaming, Sun, Xiaomin, Chen, Yucai
Publicado 2020

Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms

por Luo, Xiaona, Sun, Xiaoang, Wang, Yilin, Lin, Longlong, Yuan, Fang, Wang, Simei, Zhang, Wenjing, Ji, Xiaobing, Liu, Meiyan, Wu, Shengnan, Lan, Xiaoping, Zhang, Jie, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Publicado 2022

Segawa syndrome caused by TH gene mutation and its mechanism

por Wang, Yilin, Wang, Chunmei, Liu, Meiyan, Xu, Wuhen, Wang, Simei, Yuan, Fang, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Wang, Anqi, Guo, Miao, Lin, Longlong, Wang, Chao, Cheng, Hongyi, Liu, Zhiping, Zhang, Yuanfeng, Zeng, Fanyi, Yan, Jingbin, Chen, Yucai
Publicado 2022

Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene

por Luo, Xiaona, Wang, Chunmei, Lin, Longlong, Yuan, Fang, Wang, Simei, Wang, Yilin, Wang, Anqi, Wang, Chao, Wu, Shengnan, Lan, Xiaoping, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Xi, Jiaming, Zhang, Jie, Sun, Xiaomin, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Publicado 2021