Hasil Pencarian - Nai-Qing Cai

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  1. 1
    Altered corticalfunctional networks in Wilson's disease: A resting-state electroencephalogram study

    Altered corticalfunctional networks in Wilson's disease: A resting-state electroencephalogram study oleh Ru-Kai Chen, Chan Zhang, Jian-Wei Lin, Wu-Xiang Shi, Yu-Rong Li, Wan-Jin Chen, Nai-Qing Cai

    Diterbitkan 2024-11-01
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  2. 2
    A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy

    A “Triple Trouble” Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy oleh Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu

    Diterbitkan 2018-01-01
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  3. 3
    Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency

    Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency oleh Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui

    Diterbitkan 2019-07-01
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  4. 4
    A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2

    A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2 oleh Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo

    Diterbitkan 2021-11-01
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