Levodopa-Induced Ocular Dyskinesia in an Early-Onset Parkinson Disease Patient With GBA Mutation

por He, Jia-Ming, Wu, Zhi-Bo, Cai, Nai-Qing, Lin, Yu
Publicado 2021

Six Visual Rating Scales as A Biomarker for Monitoring Atrophied Brain Volume in Parkinson’s Disease

por Lin, Yu, Fu, Ying, Zeng, Yi-Fang, Hu, Jian-Ping, Lin, Xiao-Zhen, Cai, Nai-Qing, Weng, Qiang, Zhao, Yi-Jing, Lin, Yi, Cao, Dai-Rong, Wang, Ning
Publicado 2020

A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy

por Lin, Xiao-Dan, He, Jun-Jie, Lin, Feng, Chen, Hai-Zhu, Xu, Liu-Qing, Hu, Wei, Cai, Nai-Qing, Lin, Min-Ting, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Publicado 2018

Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency

por Chen, Hai-Zhu, Jin, Ming, Cai, Nai-Qing, Lin, Xiao-Dan, Liu, Xin-Yi, Xu, Liu-Qing, Lin, Min-Ting, Lin, Feng, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Publicado 2019

A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2

por Qiu, Liang-Liang, Lin, Xiao-Dan, Xu, Guo-Rong, Wang, Li-Li, Ye, Zhi-Xian, Lin, Feng, Chen, Hai-Zhu, Lin, Min-Ting, Cai, Nai-Qing, Jin, Ming, Xu, Liu-Qing, Hu, Wei, Wang, Ning, Wang, Zhi-Qiang
Publicado 2021