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European Journal of Neurology|June 13, 2025
Nerve Diameter and DTI Parameters Maybe Potential Markers for Clinical Trial in Patients With Charcot-Marie-Tooth Disease Type 1AYuchen Zhu, Xingwen Sun, Dongsheng Fan, et al.
Frontiers in Genetics|July 31, 2023
Clinical and mutational spectrum of paediatric Charcot-Marie-Tooth disease in a large cohort of Chinese patientsYan Ma, Xiaohui Duan, Xiaoxuan Liu, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 21, 2021
Human endogenous retrovirus K (HERV-K) env in neuronal extracellular vesicles: a new biomarker of motor neuron diseaseYuan Li, Yong Chen, Nan Zhang, et al.
Frontiers in Neurology|June 6, 2022
Differentiating Slowly Progressive Subtype of Lower Limb Onset ALS From Typical ALS Depends on the Time of Disease Progression and PhenotypeHuagang Zhang, Lu Chen, Jinzhou Tian, et al.
Frontiers in Neurology|July 15, 2022
Comparison of Slow and Forced Vital Capacity on Ability to Evaluate Respiratory Function in Bulbar-Involved Amyotrophic Lateral SclerosisXin Huang, Chenfang Du, Qiong Yang, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University|January 29, 2021
[Rare variants of HSPB1 are probably associated with amyotrophic lateral sclerosis]Junyi Chen, Xiangyi Liu, Yingsheng Xu, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 7, 2022
A de novo c.113 T > C: p.L38R mutation of SPTLC1: case report of a girl with sporadic juvenile amyotrophic lateral sclerosisXiaoxuan Liu, Ji He, Weiyi Yu, et al.
Frontiers in Neuroscience|June 25, 2019
Increased Interleukin-6 Levels in the Astrocyte-Derived Exosomes of Sporadic Amyotrophic Lateral Sclerosis PatientsYong Chen, Kailin Xia, Lu Chen, et al.
Scientific Reports|November 16, 2024
Lower creatinine-to-cystatin c ratio associated with increased risk of incident amyotrophic lateral sclerosis in the prospective UK biobank cohortZhuoya Wang, Wen Cao, Binbin Deng, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 7, 2021
An identical DCTN1 mutation in two Chinese siblings manifest as dHMN and ALS respectively: a case reportJi He, Weiyi Yu, Xiaoxuan Liu, et al.
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