Hasil Pencarian - Yu-Wei Da

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  1. 1
    CLIPPERS syndrome with cerebral cortex lesions: one case report

    CLIPPERS syndrome with cerebral cortex lesions: one case report oleh Fa-xiu SHEN, Yu-wei DA, Hai CHEN

    Diterbitkan 2019-04-01
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  2. 2
    Clinical analysis on 75 cases of subacute combined degeneration of the spinal cord

    Clinical analysis on 75 cases of subacute combined degeneration of the spinal cord oleh Bao-yi LIANG, Jian-wei YANG, Hai CHEN, Yu-wei DA

    Diterbitkan 2019-04-01
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  3. 3
    An unusual case with myotonia

    An unusual case with myotonia oleh Yu-Wei Da, Min Wang, Yun Li, Yan Lu, Jian-Ping Jia

    Diterbitkan 2013-03-01
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  4. 4
    The clinical features of 17 patients with steroid-responsive encephalopathy associated with autoimmune thyroiditis

    The clinical features of 17 patients with steroid-responsive encephalopathy associated with autoimmune thyroiditis oleh Hai CHEN, Jian-ping JIA, Er-he XU, Xiao-fan XUE, Yu-wei DA

    Diterbitkan 2013-06-01
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  5. 5
    Analysis of clinical phenotype and genetic mutation on one case of hereditary neuropathy with liability to pressure palsies presenting brachial plexus injury as the first manifestation

    Analysis of clinical phenotype and genetic mutation on one case of hereditary neuropathy with liability to pressure palsies presenting brachial plexus injury as the first manifesta... oleh Qing LIU, Hai CHEN, Lin LEI, Wen-jia ZHU, Li DI, Yan LU, Min WANG, Suo-bin WANG, Yu-wei DA

    Diterbitkan 2018-02-01
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  6. 6
    Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis

    Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis oleh Yan Lu, Yu-Wei Da, Yong-Biao Zhang, Xin-Gang Li, Xin-Gang Li, Min Wang, Li Di, Mi Pang, Lin Lei

    Diterbitkan 2018-05-01
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  7. 7
    Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis

    Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis oleh Yan Lu, Yu-Wei Da, Yong-Biao Zhang, Xin-Gang Li, Xin-Gang Li, Min Wang, Li Di, Mi Pang, Lin Lei

    Diterbitkan 2018-08-01
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  8. 8
    Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis

    Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis oleh Lin Lei, Xin-Ming Shen, Shu-Yan Wang, Yan Lu, Suo-Bin Wang, Hai Chen, Zheng Liu, Ya-Sheng Ouyang, Jian-Ying Duo, Yu-Wei Da, Zhi-Guo Chen, Yuan-Yuan Ji

    Diterbitkan 2019-06-01
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