Hasil Pencarian - Zhi‐Ying Wu

Perbaiki Hasil
  1. 1
    Challenge and strategy in the diagnosis and treatment of Wilson's disease

    Challenge and strategy in the diagnosis and treatment of Wilson's disease oleh Yue ZHANG, Zhi⁃ying WU

    Diterbitkan 2012-06-01
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  2. 2
    Huntington Disease in Asia

    Huntington Disease in Asia oleh Miao Xu, Zhi-Ying Wu

    Diterbitkan 2015-01-01
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  3. 3
    Amyotrophic Lateral Sclerosis: Precise Diagnosis and Individualized Treatment

    Amyotrophic Lateral Sclerosis: Precise Diagnosis and Individualized Treatment oleh Qing-Qing Tao, Zhi-Ying Wu

    Diterbitkan 2017-01-01
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  4. 4
    Phenotypic variance in monozygotic twins with SCA3

    Phenotypic variance in monozygotic twins with SCA3 oleh Hua Zhao, Lu Yang, Yi Dong, Zhi‐Ying Wu

    Diterbitkan 2020-10-01
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  5. 5
    Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy.

    Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy. oleh Wang Ni, Sheng Chen, Kai Qiao, Ning Wang, Zhi-Ying Wu

    Diterbitkan 2015-01-01
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  6. 6
    A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient

    A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient oleh Hao Yu, Yu-Chao Chen, Gong-Lu Liu, Zhi-Ying Wu

    Diterbitkan 2017-01-01
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  7. 7
    A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease

    A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease oleh Li-Xi Li, Hai-Lin Dong, Bao-Guo Xiao, Zhi-Ying Wu

    Diterbitkan 2017-01-01
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  8. 8
    Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population.

    Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population. oleh Shi-Rui Gan, Wang Ni, Yi Dong, Ning Wang, Zhi-Ying Wu

    Diterbitkan 2015-01-01
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  9. 9
    Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations

    Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations oleh Peishan Wang, Qiao Wei, Hongfu Li, Zhi-Ying Wu, Rongman Jia, Xiuyuan Hao

    Diterbitkan 2023-01-01
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  10. 10
    Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy

    Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy oleh Hai-Lin Dong, Jia-Qi Li, Gong-Lu Liu, Hao Yu, Zhi-Ying Wu

    Diterbitkan 2021-01-01
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  11. 11
    Acute-Onset Visual Impairment in Wilson's Disease: A Case Report and Literature Review

    Acute-Onset Visual Impairment in Wilson's Disease: A Case Report and Literature Review oleh Zi-Wei Zheng, Meng-Hui Xu, Chuan-Bin Sun, Zhi-Ying Wu, Yi Dong

    Diterbitkan 2022-06-01
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  12. 12
    The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful.

    The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful. oleh Qi Zhou, Wang Ni, Yi Dong, Ning Wang, Shi-Rui Gan, Zhi-Ying Wu

    Diterbitkan 2014-01-01
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  13. 13
    Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients

    Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients oleh Hong-Xia Wang, Hong-Fu Li, Gong-Lu Liu, Xiao-Dan Wen, Zhi-Ying Wu

    Diterbitkan 2016-01-01
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  14. 14
    Genotype-phenotype correlation and founder effect analysis in southeast Chinese patients with sialidosis type I

    Genotype-phenotype correlation and founder effect analysis in southeast Chinese patients with sialidosis type I oleh Yi-Chu Du, Ling-Han Ma, Quan-Fu Li, Yin Ma, Yi Dong, Zhi-Ying Wu

    Diterbitkan 2024-09-01
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  15. 15
    Clinical and genetic characteristics of Chinese patients with cerebrotendinous xanthomatosis

    Clinical and genetic characteristics of Chinese patients with cerebrotendinous xanthomatosis oleh Qing-Qing Tao, Yun Zhang, Hui-Xia Lin, Hai-Lin Dong, Wang Ni, Zhi-Ying Wu

    Diterbitkan 2019-12-01
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  16. 16
    Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants

    Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants oleh Pei-Shan Wang, Xin-Xia Yang, Qiao Wei, Yong-Ting Lv, Zhi-Ying Wu, Hong-Fu Li

    Diterbitkan 2024-12-01
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  17. 17
    Variants of Interferon Regulatory Factor 5 are Associated with Neither Neuromyelitis Optica Nor Multiple Sclerosis in the Southeastern Han Chinese Population

    Variants of Interferon Regulatory Factor 5 are Associated with Neither Neuromyelitis Optica Nor Multiple Sclerosis in the Southeastern Han Chinese Population oleh Qi-Bing Liu, Lei Wu, Gui-Xian Zhao, Ping-Ping Cai, Zhen-Xin Li, Zhi-Ying Wu

    Diterbitkan 2015-01-01
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  18. 18
    A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia

    A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia oleh Qiao Wei, Pei‐Shan Wang, Hai‐Lin Dong, Wen‐Jiao Luo, Zhi‐Ying Wu, Hong‐Fu Li

    Diterbitkan 2022-05-01
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  19. 19
    Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration

    Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration oleh Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue, Zhi-Ying Wu, Hong-Fu Li, Ning Wang

    Diterbitkan 2022-04-01
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  20. 20
    Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3

    Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3 oleh Quan-Fu Li, Hao‐Ling Cheng, Lu Yang, Yin Ma, Jing‐Jing Zhao, Yi Dong, Zhi‐Ying Wu

    Diterbitkan 2020-09-01
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