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Frontiers in Neurology|May 19, 2017
Resistant Hypertension after Hypertensive Intracerebral Hemorrhage Is Associated with More Medical Interventions and Longer Hospital Stays without Affecting OutcomeDaojun Hong, Dana Stradling, Cyrus K Dastur, et al.Journal of Human Genetics|August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodesDanhua Zhao, Daojun Hong, Wei Zhang, et al.Journal of the Neurological Sciences|November 15, 2019
Patients with MELAS with negative myopathology for characteristic ragged-red fibersYuanyuan Lu, Jianwen Deng, Yuying Zhao, et al.Clinical Neuropathology|October 30, 2019
Diagnostic indicators for adult-onset neuronal intranuclear inclusion diseaseYan Wang, Bo Wang, Lu Wang, et al.Journal of the Neurological Sciences|July 19, 2017
Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathyYuanyuan Lu, Danhua Zhao, Sheng Yao, et al.CNS Neuroscience & Therapeutics|March 6, 2025
Akkermansia muciniphila Modulates Central Nervous System Autoimmune Response and Cognitive Impairment by Inhibiting Hippocampal NLRP3-Mediated NeuroinflammationXiaobing Li, Dengna Lin, Xin Hu, et al.Annals of Clinical and Translational Neurology|January 13, 2026
Diffusion Spectrum Imaging Maps Early Axonal Loss and a Unique Progressive Signal in Neuronal Intranuclear Inclusion DiseaseKaiyan Jiang, Yixiu Pei, Xiaobao Hu, et al.Cell Communication and Signaling : CCS|February 7, 2025
uN2CpolyG-mediated p65 nuclear sequestration suppresses the NF-κB-NLRP3 pathway in neuronal intranuclear inclusion diseaseYu Shen, Kaiyan Jiang, Dandan Tan, et al.Proceedings of the National Academy of Sciences of the United States of America|October 3, 2022
CGG repeat expansion in <i>NOTCH2NLC</i> causes mitochondrial dysfunction and progressive neurodegeneration in <i>Drosophila</i> modelJiaxi Yu, Tongling Liufu, Yilei Zheng, et al.Journal of Neuromuscular Diseases|February 20, 2025
Mutational and clinical spectrum of myofibrillar myopathy in one center from ChinaQi Wang, Peng Sun, Meng Yu, et al.Pageof 15