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Neurocritical Care|May 19, 2023
Aquaporin 4 Mediates the Effect of Iron Overload on Hydrocephalus After Intraventricular HemorrhageYing Li, Ding Nan, Ran Liu, et al.Annals of Clinical and Translational Neurology|September 24, 2022
Subsarcolemmal and cytoplasmic p62 positivity and rimmed vacuoles are distinctive for PLIN4-myopathyQi Wang, Meng Yu, Wei Zhang, et al.Journal of Medical Genetics|February 27, 2024
Novel <i>TUBA4A</i> variant causes congenital myopathy with focal myofibrillar disorganisationYalan Wan, Chao Zhou, Xingzhi Chang, et al.Frontiers in Genetics|July 26, 2021
GGC Repeat Expansion in the <i>NOTCH2NLC</i> Gene Is Associated With a Phenotype of Predominant Motor-Sensory and Autonomic NeuropathyHui Wang, Jiaxi Yu, Meng Yu, et al.Neuromuscular Disorders : NMD|January 9, 2024
A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophyZhiying Xie, Chengyue Sun, Chang Liu, 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.Journal of Neurology|April 29, 2022
Circulating cell-free mtDNA release is associated with the activation of cGAS-STING pathway and inflammation in mitochondrial diseasesXutong Zhao, Meng Yu, Yawen Zhao, et al.European Journal of Neurology|September 26, 2024
Elevated serum circulating cell-free mitochondrial DNA in amyotrophic lateral sclerosisJieyu Li, Chao Gao, Qingqing Wang, et al.Frontiers in Immunology|March 23, 2026
The clinical, serological and myopathological features of a cohort of Chinese patients with inclusion body myositis: a single center analysisHongyan Qiu, Shouzheng Yang, Xuejun Guo, et al.Pageof 11