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Human Molecular Genetics|May 14, 2021
Increasing LRP4 diminishes neuromuscular deficits in a mouse model of Duchenne muscular dystrophyTiankun Hui, Hongyang Jing, Tian Zhou, et al.
Brain and Behavior|April 21, 2020
FUS P525L mutation causing amyotrophic lateral sclerosis and movement disordersBinbin Zhou, Huan Wang, Yu Cai, et al.
Brain and Behavior|March 2, 2021
Benign monomelic amyotrophy of lower limb in a cohort of chinese patientsLulu Wang, Han Wen, Shuyun Chen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 27, 2024
Encephalitis-like episodes with cortical edema and enhancement in patients with neuronal intranuclear inclusion diseaseYu Shen, Kaiyan Jiang, Hanlin Liang, et al.
Biomed Research International|January 6, 2023
Lymphocyte-to-Monocyte Ratio Is Independently Associated with Progressive Infarction in Patients with Acute Ischemic StrokeXiaocheng Mao, Qiulong Yu, Yunfang Liao, et al.
Frontiers in Neuroscience|December 24, 2019
Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral SclerosisJianwen Deng, Wei Wu, Zhiying Xie, et al.
European Journal of Neurology|October 20, 2022
Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathyDaojun Hong, Hui Wang, Min Zhu, et al.
Molecular Neurobiology|September 28, 2022
FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALSBinbin Zhou, Yilei Zheng, Xiaobing Li, et al.
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