Hasil Pencarian - Cuijie Wei

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  1. 1
    Treatment of childhood intraneural perineurioma: A case report and literature review

    Treatment of childhood intraneural perineurioma: A case report and literature review oleh Rongpei Li, Yao Zhang, Guanggui Li, Cuijie Wei, Hui Xiong, Xingzhi Chang

    Diterbitkan 2024-03-01
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  2. 2
    Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre

    Clinical and genetic features of infancy-onset congenital myopathies from a Chinese paediatric centre oleh Yu Zhang, Hui Yan, Jieyu Liu, Huifang Yan, Yinan Ma, Cuijie Wei, Zhaoxia Wang, Hui Xiong, Xingzhi Chang

    Diterbitkan 2022-01-01
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  3. 3
    Correlation of Phenotype–Genotype and Protein Structure in RYR1-Related Myopathy

    Correlation of Phenotype–Genotype and Protein Structure in RYR1-Related Myopathy oleh Xingzhi Chang, Risheng Wei, Cuijie Wei, Jieyu Liu, Lun Qin, Hui Yan, Yinan Ma, Zhaoxia Wang, Hui Xiong

    Diterbitkan 2022-05-01
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  4. 4
    HPLC-PDA combined with chemometrics for chemical markers of Paeoniae Radix Alba before and after sulfur-fumigated

    HPLC-PDA combined with chemometrics for chemical markers of Paeoniae Radix Alba before and after sulfur-fumigated oleh Xiaozhou Jia, Yueyi Liang, Fang Chen, Xiaoxia Liu, Cuijie Wei, Qing Ding, Xiangdong Chen, Dongmei Sun, Mei Wei

    Diterbitkan 2021-01-01
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  5. 5
    Scoliosis Orthopedic Surgery Combined With Nusinersen Intrathecal Injection Significantly Improved the Outcome of Spinal Muscular Atrophy Patient: A Case Report

    Scoliosis Orthopedic Surgery Combined With Nusinersen Intrathecal Injection Significantly Improved the Outcome of Spinal Muscular Atrophy Patient: A Case Report oleh Beiyu Xu, Cuijie Wei, Xiao Hu, Wenzhu Li, Zhen Huang, Chengli Que, Jianxing Qiu, Chunde Li, Hui Xiong

    Diterbitkan 2022-04-01
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  6. 6
    Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis

    Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis oleh Cuijie Wei, Zhenwei Liang, Ying Wu, Shan Liu, Jianxing Qiu, Lingchao Meng, Chunde Li, Shuang Li, Xinhua Bao, Zhaoxia Wang, Luzeng Chen, Hui Xiong

    Diterbitkan 2023-02-01
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  7. 7
    Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients

    Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients oleh Xiuli Huang, Dandan Tan, Zaiqiang Zhang, Lin Ge, Jieyu Liu, Juan Ding, Haipo Yang, Cuijie Wei, Xingzhi Chang, Yun Yuan, Chuanzhu Yan, Hui Xiong, Hui Xiong

    Diterbitkan 2023-05-01
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  8. 8
    Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients

    Novel SEPN1 Mutations in Exon 1 Are Common in Rigid Spine With Muscular Dystrophy Type 1 in Chinese Patients oleh Yanbin Fan, Zhifei Xu, Xing Li, Feng Gao, Enyu Guo, Xingzhi Chang, Cuijie Wei, Cheng Zhang, Qing Yu, Chengli Que, Jiangxi Xiao, Chuanzhu Yan, Zhaoxia Wang, Yun Yuan, Hui Xiong

    Diterbitkan 2022-03-01
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  9. 9
    Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy

    Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy oleh Shu Zhang, Dongdong Qin, Liwen Wu, Man Li, Lifang Song, Cuijie Wei, Chunling Lu, Xiaoli Zhang, Siqi Hong, Mingming Ma, Shiwen Wu, National DMD Research Network of “One City, One Doctor”

    Diterbitkan 2021-04-01
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  10. 10
    Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers

    Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers oleh Jianzhao Zhang, Taoyun Ji, Qian Chen, Yanan Jiang, Huan Cheng, Ping Zheng, Wenqiang Ma, Ting Lei, Yao Zhang, Yiwen Jin, Cuijie Wei, Ye Wu, Xingzhi Chang, Xinhua Bao, Yuehua Zhang, Hui Xiong, Xinna Ji, Shuo Feng, Haitao Ren, Jian Yang, Yuwu Jiang

    Diterbitkan 2019-08-01
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  11. 11
    Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

    Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort oleh Dandan Tan, Lin Ge, Yanbin Fan, Xingzhi Chang, Shuang Wang, Cuijie Wei, Juan Ding, Aijie Liu, Shuo Wang, Xueying Li, Kai Gao, Haipo Yang, Chengli Que, Zhen Huang, Chunde Li, Ying Zhu, Bing Mao, Bo Jin, Ying Hua, Xiaoli Zhang, Bingbing Zhang, Wenhua Zhu, Cheng Zhang, Yanjuan Wang, Yun Yuan, Yuwu Jiang, Anne Rutkowski, Carsten G. Bönnemann, Xiru Wu, Hui Xiong

    Diterbitkan 2021-07-01
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