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Lin Lei

Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain
2019 · Yanan Sun, Hai Chen, et al. · Journal of Neurology · 42
Favorable Effects of Tacrolimus Monotherapy on Myasthenia Gravis Patients
2020 · Zhirong Fan, Zunbo Li, et al. · Frontiers in Neurology · 31
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VNTR2/VNTR3 genotype in the FCGRT gene is associated with reduced effectiveness of intravenous immunoglobulin in patients with myasthenia gravis
2021 · Shengyao Su, Qing Liu, et al. · Therapeutic Advances in Neurological Disorders · 29
Clinical Predictors of Relapse in a Cohort of Steroid-Treated Patients With Well-Controlled Myasthenia Gravis
2022 · Shengyao Su, Lin Lei, et al. · Frontiers in Neurology · 16
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Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy
2017 · Min Wang, Lin Lei, et al. · Neuromuscular Disorders · 14
Comparison between mono‐tacrolimus and mono‐glucocorticoid in the treatment of myasthenia gravis
2023 · Zhirong Fan, Lin Lei, et al. · Annals of Clinical and Translational Neurology · 13
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Environmental factors affecting the risk of generalization for ocular-onset myasthenia gravis: a nationwide cohort study
2023 · Jingsi Wang, Hongyu Zhou, et al. · QJM · 11
Delayed Respiratory Insufficiency and Extramuscular Abnormalities in Selenoprotein N-Related Myopathies
2021 · Shu Zhang, Lin Lei, et al. · Frontiers in Neurology · 9
Nomogram for short-term outcome assessment in AChR subtype generalized myasthenia gravis
2021 · Rui Zhao, Ying Wang, et al. · Journal of Translational Medicine · 9
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Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis
2019 · Lin Lei, Xin-Ming Shen, et al. · Chinese Medical Journal · 7
Unusual electrophysiological findings in a Chinese ALS 4 family with SETX-L389S mutation: a three-year follow-up
2020 · Lin Lei, Hai Chen, et al. · Journal of Neurology · 4
Successful treatment of periodic paralysis with coenzyme Q10: two case reports.
2016 · Yuwei Da, Lin Lei, et al. · PubMed · 3
CYP3A5*3 polymorphism and age affect tacrolimus blood trough concentration in myasthenia gravis patients
2021 · Zhirong Fan, Deqiang Zheng, et al. · Journal of Neuroimmunology · 2
Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
2018 · Yan Lu, Yu-Wei Da, et al. · Frontiers in Neuroscience · 1
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Association between neutrophil-to-lymphocyte ratio and cerebral small vessel disease: a systematic review and meta-analysis
2026 · Qian You, Ying Li, et al. · Frontiers in Neurology
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The association between bone turnover biomarkers and the severity of white matter hyperintensities
2025 · Qian You, Ying Li, et al. · Frontiers in Neurology
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Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
2018 · Yan Lu, Yu-Wei Da, et al. · Frontiers in Neuroscience
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Analysis of clinical phenotype and genetic mutation on one case of hereditary neuropathy with liability to pressure palsies presenting brachial plexus injury as the first manifestation
2018 · Qing LIU, Hai CHEN, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Recent advance in treatment of refractory myasthenia gravis
2016 · Lin Lei · Chinese Journal of Neuromedicine
Works count: 21
Citation count: 191
H-index: 9
I10-index: 7
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