Zoekresultaten - Pu, Chuan-Qiang

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  1. 1
    Complement membrane attack complex is related with immune-mediated necrotizing myopathy

    Complement membrane attack complex is related with immune-mediated necrotizing myopathy door Cong, Lu, Pu, Chuan-Qiang, Shi, Qiang, Wang, Qian, Lu, Xiang-Hui

    Gepubliceerd in 2014
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  2. 2
    Increased Expression of the NOD-like Receptor Family, Pyrin Domain Containing 3 Inflammasome in Dermatomyositis and Polymyositis is a Potential Contributor to Their Pathogenesis

    Increased Expression of the NOD-like Receptor Family, Pyrin Domain Containing 3 Inflammasome in Dermatomyositis and Polymyositis is a Potential Contributor to Their Pathogenesis door Yin, Xi, Han, Gen-Cheng, Jiang, Xing-Wei, Shi, Qiang, Pu, Chuan-Qiang

    Gepubliceerd in 2016
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  3. 3
    Identification of Seven Novel Mutations in the Acid Alpha-glucosidase Gene in Five Chinese Patients with Late-onset Pompe Disease

    Identification of Seven Novel Mutations in the Acid Alpha-glucosidase Gene in Five Chinese Patients with Late-onset Pompe Disease door Liu, Hua-Xu, Pu, Chuan-Qiang, Shi, Qiang, Zhang, Yu-Tong, Ban, Rui

    Gepubliceerd in 2018
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  4. 4
    A Novel Mutation of Mitochondrial T14709C Causes Myoclonic Epilepsy with Ragged Red Fibers Syndrome in a Chinese Patient

    A Novel Mutation of Mitochondrial T14709C Causes Myoclonic Epilepsy with Ragged Red Fibers Syndrome in a Chinese Patient door Ban, Rui, Guo, Jun-Hong, Pu, Chuan-Qiang, Shi, Qiang, Liu, Hua-Xu, Zhang, Yu-Tong

    Gepubliceerd in 2018
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  5. 5
    Reply to “Mitochondrial tRNA Glutamic Acid Variant 14709T>C Manifesting as Myoclonic Epilepsy with Ragged Red Fibers”

    Reply to “Mitochondrial tRNA Glutamic Acid Variant 14709T>C Manifesting as Myoclonic Epilepsy with Ragged Red Fibers” door Ban, Rui, Guo, Jun-Hong, Pu, Chuan-Qiang, Shi, Qiang, Liu, Hua-Xu, Zhang, Yu-Tong

    Gepubliceerd in 2018
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  6. 6
    Clinical, Pathological, and Genetic Features of Two Chinese Cases with Filamin C Myopathy

    Clinical, Pathological, and Genetic Features of Two Chinese Cases with Filamin C Myopathy door Zhang, Yu-Tong, Pu, Chuan-Qiang, Ban, Rui, Liu, Hua-Xu, Shi, Qiang, Lu, Xiang-Hui

    Gepubliceerd in 2018
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  7. 7
    A Novel AGRN Mutation Leads to Congenital Myasthenic Syndrome Only Affecting Limb-girdle Muscle

    A Novel AGRN Mutation Leads to Congenital Myasthenic Syndrome Only Affecting Limb-girdle Muscle door Zhang, Ying, Dai, Yi, Han, Jing-Na, Chen, Zhao-Hui, Ling, Li, Pu, Chuan-Qiang, Cui, Li-Ying, Huang, Xu-Sheng

    Gepubliceerd in 2017
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  8. 8
    Oculopharyngeal Weakness, Hypophrenia, Deafness, and Impaired Vision: A Novel Autosomal Dominant Myopathy with Rimmed Vacuoles

    Oculopharyngeal Weakness, Hypophrenia, Deafness, and Impaired Vision: A Novel Autosomal Dominant Myopathy with Rimmed Vacuoles door Chen, Ting, Lu, Xiang-Hui, Wang, Hui-Fang, Ban, Rui, Liu, Hua-Xu, Shi, Qiang, Wang, Qian, Yin, Xi, Pu, Chuan-Qiang

    Gepubliceerd in 2016
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  9. 9
    Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases

    Chinese Specific Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Analysis of 57 Cases door Zhao, Wei, Zhang, Jia-Tang, Xing, Xiao-Wei, Huang, De-Hui, Tian, Cheng-Lin, Jia, Wei-Quan, Huang, Xu-Sheng, Wu, Wei-Ping, Pu, Chuan-Qiang, Lang, Sen-Yang, Yu, Sheng-Yuan

    Gepubliceerd in 2013
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  10. 10
    HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy

    HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy door Li, Moyi, Zhuang, Yan, Batra, Ranjan, Thomas, James D., Li, Mao, Nutter, Curtis A., Scotti, Marina M., Carter, Helmut A., Wang, Zhan Jun, Huang, Xu-Sheng, Pu, Chuan Qiang, Swanson, Maurice S., Xie, Wei

    Gepubliceerd in 2020
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