Serum Uric Acid Levels Predict Mortality Risk in Male Amyotrophic Lateral Sclerosis Patients

por Xu, Liu-Qing, Hu, Wei, Guo, Qi-Fu, Xu, Guo-Rong, Wang, Ning, Zhang, Qi-Jie
Publicado 2021

Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis

por Xu, Liu-Qing, Hu, Wei, Guo, Qi-Fu, Lai, Lu-Lu, Xu, Guo-Rong, Chen, Wan-Jin, Wang, Ning, Zhang, Qi-Jie
Publicado 2020

High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis

por Xu, Guo-rong, Hu, Wei, Zhan, Ling-Ling, Wang, Chong, Xu, Liu-Qing, Lin, Min-Ting, Chen, Wan-Jin, Wang, Ning, Zhang, Qi-Jie
Publicado 2018

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