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Human Molecular Genetics|February 23, 2026
An Alu mediated intergenic inversion in RBCK1 causing Polyglucosan body myopathy type 1Bochen Zhu, Kexin Jiao, Xiaona Luo, et al.
The Journal of Molecular Diagnostics : JMD|March 15, 2024
Diagnosis of Challenging Spinal Muscular Atrophy Cases with Long-Read SequencingNingning Wang, Kexin Jiao, Jin He, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|October 1, 2019
Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle ChannelopathiesJian Sun, Sushan Luo, Jie Song, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 11, 2025
KFLC-index distinguishes multiple sclerosis from anti-myelin oligodendrocyte glycoprotein and aquaporin 4 diseases in a Chinese cohortHongmei Tan, Xuan Deng, Jingzi ZhangBao, et al.
Multiple Sclerosis and Related Disorders|March 28, 2022
Efficacy and safety of rehabilitation exercise in neuromyelitis optica spectrum disorder during the acute phase: A prospective cohort studyQinying Li, Bei Wang, Bingyuan Cheng, et al.
Frontiers in Immunology|January 22, 2026
Dysregulated Tfh/B cells and their interactions in neuromyelitis optica spectrum disorderLiang Wang, Lei Zhou, Zhouzhou Wang, et al.
Journal of Human Genetics|June 29, 2025
Pseudoexon activating by a deep intronic variant and phenotype variation in a Chinese family with dystrophinopathyXingyu Xia, Kexin Jiao, Chaoping Hu, et al.
Therapeutic Advances in Neurological Disorders|July 29, 2024
The safety and efficacy profile of eculizumab in myasthenic crisis: a prospective small case seriesJie Song, Xiao Huan, Yuanyi Chen, et al.
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