Showing 1 - 19 results of 19 for search 'Wan‐Jin Chen', query time: 0.04s Refine Results
  1. 1
    The research progress of clinical diagnosis of spinal muscular atrophy

    The research progress of clinical diagnosis of spinal muscular atrophy by Ning WANG, Jin HE, Wan⁃jin CHEN

    Published 2012-06-01
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  2. 2
    Ten⁃year advance in the genomics study on neuropathic hereditary diseases

    Ten⁃year advance in the genomics study on neuropathic hereditary diseases by Ning WANG, Yu LIN, Wan⁃jin CHEN

    Published 2010-02-01
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  3. 3
    Research progress of spinal muscular atrophy treatment in children

    Research progress of spinal muscular atrophy treatment in children by Miao ZHAO, Ying-qian LU, Ning WANG, Wan-jin CHEN

    Published 2018-04-01
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  4. 4
    Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth disease

    Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth disease by Jin HE, Guo-rong XU, Han LIN, Ning WANG, Wan-jin CHEN

    Published 2017-08-01
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  5. 5
    Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis

    Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis by Liu-Qing Xu, Wei Hu, Qi-Fu Guo, Lu-Lu Lai, Guo-Rong Xu, Wan-Jin Chen, Wan-Jin Chen, Ning Wang, Ning Wang, Qi-Jie Zhang, Qi-Jie Zhang

    Published 2020-10-01
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  6. 6
    Progress in research on molecular mechanism of facioscapulohumeral muscular dystrophy

    Progress in research on molecular mechanism of facioscapulohumeral muscular dystrophy by Xiao-dan LIN, Jun-jie HE, Wan-jin CHEN, Ning WANG, Zhi-qiang WANG

    Published 2017-08-01
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  7. 7
    Studies on the prenatal diagnosis of spinal muscular atrophy by multiplex ligation⁃dependent probe amplification

    Studies on the prenatal diagnosis of spinal muscular atrophy by multiplex ligation⁃dependent probe amplification by Ya⁃fang CHEN, Jin HE, Qi⁃jie ZHANG, Xiang LIN, Ning WANG, Wan⁃jin CHEN

    Published 2012-06-01
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  8. 8
    Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson′s Disease in Han Chinese

    Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson′s Disease in Han Chinese by Ya-Fang Chen, Wan-Jin Chen, Xiao-Zhen Lin, Qi-Jie Zhang, Jiang-Ping Cai, Chia-Wei Liou, Ning Wang

    Published 2015-01-01
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  9. 9
    Potential markers for sample size estimations in hereditary spastic paraplegia type 5

    Potential markers for sample size estimations in hereditary spastic paraplegia type 5 by Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu

    Published 2021-09-01
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  10. 10
    Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5

    Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5 by Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu

    Published 2021-10-01
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  11. 11
    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mu... by Ying-qian Lu, En-lin Dong, Wei-qi Yang, Lu-lu Lai, Xiao-hong Lin, Li-xiang Ma, Wan-jin Chen, Ning Wang, Xiang Lin

    Published 2019-01-01
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  12. 12
    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia by Lu‐Lu Lai, Yi‐Jun Chen, Yun‐Lu Li, Xiao‐Hong Lin, Meng‐Wen Wang, En‐Lin Dong, Ning Wang, Wan‐Jin Chen, Xiang Lin

    Published 2020-10-01
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  13. 13
    Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification

    Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification by Yi-Heng Zeng, Bi-Wei Lin, Hui-Zhen Su, Xin-Xin Guo, Yun-Lu Li, Lu-Lu Lai, Wan-Jin Chen, Miao Zhao, Xiang-Ping Yao

    Published 2021-10-01
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  14. 14
    Knockdown of myorg leads to brain calcification in zebrafish

    Knockdown of myorg leads to brain calcification in zebrafish by Miao Zhao, Xiao-Hong Lin, Yi-Heng Zeng, Hui-Zhen Su, Chong Wang, Kang Yang, Yi-Kun Chen, Bi-Wei Lin, Xiang-Ping Yao, Wan-Jin Chen

    Published 2022-07-01
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  15. 15
    Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients

    Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients by Jin-Shan Yang, Hao-Ling Xu, Ping-Ping Chen, Arif Sikandar, Mei-Zhen Qian, Hui-Xia Lin, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Hua Wu, Shi-Rui Gan

    Published 2020-04-01
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  16. 16
    Quantitative assessment of postural instability in spinocerebellar ataxia type 3 patients

    Quantitative assessment of postural instability in spinocerebellar ataxia type 3 patients by Xia‐Hua Liu, Ying Li, Hao‐Ling Xu, Arif Sikandar, Wei‐Hong Lin, Gui‐He Li, Xiao‐Fen Li, Alimire Alimu, Sheng‐Bin Yu, Xiang‐Hui Ye, Ning Wang, Jun Ni, Wan‐Jin Chen, Shi‐Rui Gan

    Published 2020-08-01
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  17. 17
    Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study

    Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study by Xiang Lin, Ying Liu, Yi Lin, Ning Wang, Wan-Jin Chen, Ying Fu, Xiao-Hong Lin, Yu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, Zhi-Xian Ye, Jin Bi, Yi-Jun Chen, Meng-Wen Wang, Shao-Bo Yao, Yi-Kun Chen, Jun-Yi Jiang

    Published 2022-01-01
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  18. 18
    Exhausting T Cells During HIV Infection May Improve the Prognosis of Patients with COVID-19

    Exhausting T Cells During HIV Infection May Improve the Prognosis of Patients with COVID-19 by Hua-Song Lin, Xiao-Hong Lin, Jian-Wen Wang, Dan-Ning Wen, Jie Xiang, Yan-Qing Fan, Hua-Dong Li, Jing Wu, Yi Lin, Ya-Lan Lin, Xu-Ri Sun, Yun-Feng Chen, Chuan-Juan Chen, Ning-Fang Lian, Han-Sheng Xie, Shou-Hong Lin, Qun-Fang Xie, Chao-Wei Li, Fang-Zhan Peng, Ning Wang, Jian-Qing Lin, Wan-Jin Chen, Chao-Lin Huang, Ying Fu, Ying Fu

    Published 2021-09-01
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  19. 19
    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification

    Loss of function of CMPK2 causes mitochondria deficiency and brain calcification by Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen

    Published 2022-11-01
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