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Neuromuscular Disorders : NMD|April 24, 2017
Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndromeSushan Luo, Shuang Cai, Susan Maxwell, et al.
Therapeutic Advances in Neurological Disorders|February 12, 2024
Independent risk factors for in-hospital outcome of myasthenic crisis: a prospective cohort studyYuan Wang, Xiao Huan, Xinfang Zhu, et al.
Neurology India|January 17, 2015
Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathyJianying Xi, Gaelle Blandin, Jiahong Lu, et al.
Neuromuscular Disorders : NMD|July 28, 2019
Clinical spectrum and gene mutations in a Chinese cohort with anoctaminopathyShuang Cai, Mingshi Gao, Jianying Xi, et al.
Annals of Clinical and Translational Neurology|February 22, 2021
In-depth peripheral CD4<sup>+</sup> T profile correlates with myasthenic crisisXiao Huan, Sushan Luo, Huahua Zhong, et al.
Clinical Immunology (Orlando, Fla.)|August 23, 2025
Efgartigimod versus standard of care in new-Onset AChR subtype generalized myasthenia gravis: A prospective cohort studyDingxian He, Lei Jin, Shuangshuang Wang, et al.
Muscle & Nerve|March 21, 2021
Short-term effect of low-dose rituximab on myasthenia gravis with muscle-specific tyrosine kinase antibodyYufan Zhou, Chong Yan, Xinyu Gu, et al.
Stem Cell Research|September 2, 2022
Human-induced pluripotent stem cell line (FDHSi001-A) derived from a patient with a CGG repeat expansion in the 5'UTR of GIPC1Kexin Jiao, Dongyue Yue, Xinyu Gu, et al.
Frontiers in Neurology|April 25, 2022
Clinical Features of Myasthenia Gravis With Antibodies to MuSK Based on Age at Onset: A Multicenter Retrospective Study in ChinaYufan Zhou, Jialin Chen, Zunbo Li, et al.
BMC Neurology|May 10, 2019
Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencingSushan Luo, Minjie Xu, Jian Sun, et al.
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