Hasil Pencarian - Zeshu Ning

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  1. 1
    Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants

    Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants oleh Qingyun Kang, Hui Kang, Jingwen Tang, Miao Wang, Haojiang Jiang, Zeshu Ning, Liwen Wu

    Diterbitkan 2024-05-01
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  2. 2
    A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report

    A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report oleh Qingyun Kang, Liming Yang, Hongmei Liao, Sai Yang, Xiaojun Kuang, Zeshu Ning, Caishi Liao, Bo Chen

    Diterbitkan 2021-06-01
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  3. 3
    Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation

    Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation oleh Qingyun Kang, Liming Yang, Hongmei Liao, Sai Yang, Haiyang Yang, Zeshu Ning, Caishi Liao, Liwen Wu

    Diterbitkan 2021-12-01
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  4. 4
    Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

    Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study oleh Qingyun Kang, Hongmei Liao, Liming Yang, Hongjun Fang, Zeshu Ning, Caishi Liao, Siyi Gan, Liwen Wu

    Diterbitkan 2023-04-01
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  5. 5
    Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

    Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report oleh Sai Yang, Xiang Shen, Qingyun Kang, Xiaojun Kuang, Zeshu Ning, Shulei Liu, Hongmei Liao, Zhenhua Cao, Liming Yang

    Diterbitkan 2020-06-01
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  6. 6
    Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations

    Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations oleh Wenjing Hu, Hongjun Fang, Yu Peng, Li Li, Danni Guo, Jingwen Tang, Jurong Yi, Qingqing Liu, Wei Qin, Liwen Wu, Zeshu Ning

    Diterbitkan 2022-12-01
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  7. 7
    Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study

    Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study oleh Zhi Jiang, Hongmei Liao, Liwen Wu, Wenjing Hu, Liming Yang, Bo Chen, Zeshu Ning, Jingwen Tang, Rong Xu, Mei Chen, Feng Guo, Shulei Liu

    Diterbitkan 2023-07-01
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