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Annals of Clinical and Translational Neurology|August 21, 2019
Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathyDaojun Hong, Pu Fang, Sheng Yao, et al.
American Journal of Human Genetics|February 12, 2022
The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4Jiaxi Yu, Jingli Shan, Meng Yu, et al.
Annals of Clinical and Translational Neurology|July 8, 2024
Efgartigimod for generalized myasthenia gravis: A multicenter real-world cohort study in ChinaSushan Luo, Qilong Jiang, Wenshuang Zeng, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathyJiaxi Yu, Xing-Hua Luan, Meng Yu, et al.
Therapeutic Advances in Neurological Disorders|February 20, 2025
Patterns and predictors of therapeutic response to efgartigimod in acetylcholine receptor-antibody generalized myasthenia gravis subtypesLei Jin, Zhangyu Zou, Qinzhou Wang, et al.
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