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Neuromuscular Disorders : NMD|August 10, 2015
Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutationSushan Luo, Wenhua Zhu, Dongyue Yue, et al.Stem Cell Research|September 20, 2024
Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE geneKexin Jiao, Jialong Zhang, Ningning Wang, et al.Neuromuscular Disorders : NMD|December 16, 2014
New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failureDongyue Yue, Mingshi Gao, Wenhua Zhu, et al.Orphanet Journal of Rare Diseases|December 21, 2017
Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndromeJianying Xi, Chong Yan, Wei-Wei Liu, et al.Scientific Reports|June 28, 2018
Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4Sushan Luo, Marisol Sampedro Castañeda, Emma Matthews, et al.European Neurology|June 12, 2020
Adult Ocular Myasthenia Gravis Conversion: A Single-Center Retrospective Analysis in ChinaXuelin Feng, Xiao Huan, Chong Yan, et al.Frontiers in Neurology|February 15, 2024
Insights into refractory chronic inflammatory demyelinating polyneuropathy: a comprehensive real-world studyYongsheng Zheng, Jianian Hu, Chong Sun, et al.Combinatorial Chemistry & High Throughput Screening|March 12, 2025
The Anti-PEDV Effects and Mechanisms of Forsythia Essential Oil Based on Network Pharmacology and Experimental ValidationRuiping Liang, Jianbo Guo, Kai Li, et al.Journal of the Peripheral Nervous System : JPNS|August 17, 2024
Long-term and low-dose rituximab treatment for chronic inflammatory demyelinating polyneuropathyYongsheng Zheng, Chong Sun, Yanyin Zhao, et al.Journal of Neurology|May 17, 2023
Effectiveness and safety of rituximab in autoimmune nodopathy: a single-center cohort studyBingyou Liu, Jianian Hu, Chong Sun, et al.Pageof 22