Evaluation of SORD mutations as a novel cause of Charcot‐Marie‐Tooth disease

por Yuan, Ru‐Ying, Ye, Zi‐Ling, Zhang, Xiao‐Rong, Xu, Liu‐Qing, He, Jin
Publicado 2020

Four-year follow-up of a Wilson disease pedigree complicated with epilepsy and hypopituitarism: Case report with a literature review

por Zhang, Qi-Jie, Xu, Liu-Qing, Wang, Chong, Hu, Wei, Wang, Ning, Chen, Wan-Jin
Publicado 2016

Decreased serum creatinine levels predict short survival in amyotrophic lateral sclerosis

por Guo, Qi‐Fu, Hu, Wei, Xu, Liu‐Qing, Luo, Hao, Wang, Ning, Zhang, Qi‐Jie
Publicado 2021

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

Peak expiratory flow is a reliably household pulmonary function parameter correlates with disease severity and survival of patients with amyotrophic lateral sclerosis

por Zhang, Qi-Jie, Huang, Jian-Chai, Chen, Jia, Hu, Wei, Xu, Liu-Qing, Guo, Qi-Fu
Publicado 2022

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