Hasil Pencarian - Xue-Bi Xu

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  1. 1
    Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations

    Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations oleh Xiao-Lin Yu, Chuan-Zhu Yan, Kun-Qian Ji, Peng-Fei Lin, Xue-Bi Xu, Ting-Jun Dai, Wei Li, Yu-Ying Zhao

    Diterbitkan 2018-01-01
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  2. 2
    Activated mTOR signaling pathway in myofibers with inherited metabolic defect might be an evidence for mTOR inhibition therapies

    Activated mTOR signaling pathway in myofibers with inherited metabolic defect might be an evidence for mTOR inhibition therapies oleh Jing-Wei Lyu, Xue-Bi Xu, Kun-Qian Ji, Na Zhang, Yuan Sun, Dan-Dan Zhao, Yu-Ying Zhao, Chuan-Zhu Yan, Qiang Shi

    Diterbitkan 2019-04-01
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  3. 3
    Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

    Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation oleh Xue-Bi Xu, Kun-Qian Ji, Jing-Wei Lyu, Shu Zhang, Xiao-Qing Lyu, Chang Liu, Wei Li, Chuan-Zhu Yan, Yu-Ying Zhao, Ning-Ning Wang

    Diterbitkan 2019-03-01
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