Showing 1 - 9 results of 9 for search 'Wen-Chen Liang', query time: 0.02s Refine Results
  1. 1
    Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family

    Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family by Yen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, Yuh-Jyh Jong

    Published 2014-04-01
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  2. 2
    Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutation

    Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutation by Chen-Hua Wang, Wen-Chen Liang, Pei-Chin Lin, Yuh-Jyh Jong

    Published 2022-03-01
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  3. 3
    Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan

    Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan by Chien-Hua Wang, Wen-Chen Liang, Narihiro Minami, Ichizo Nishino, Yuh-Jyh Jong

    Published 2015-02-01
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  4. 4
    The natural history of the patients with Duchenne muscular dystrophy in Taiwan: A medical center experience

    The natural history of the patients with Duchenne muscular dystrophy in Taiwan: A medical center experience by Wen-Chen Liang, Chen-Hua Wang, Po-Ching Chou, Wan-Zi Chen, Yuh-Jyh Jong

    Published 2018-04-01
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  5. 5
    ETFDH mutation involves excessive apoptosis and neurite outgrowth defect via Bcl2 pathway

    ETFDH mutation involves excessive apoptosis and neurite outgrowth defect via Bcl2 pathway by Chuang-Yu Lin, Wen-Chen Liang, Yi-Chen Yu, Shin-Cheng Chang, Ming-Chi Lai, Yuh-Jyh Jong

    Published 2024-10-01
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  6. 6
    Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia

    Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia by Chien-Hua Wang, Wen-Chen Liang, Yi-Ning Su, Wen-Chieh Lee, Ching-Chyuan Su, Yuh-Jyh Jong

    Published 2012-12-01
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  7. 7
    Botulism with Unusual Rapid Progression to Complete Paralysis in a Child

    Botulism with Unusual Rapid Progression to Complete Paralysis in a Child by Hui-Ju Tsai, Wen-Chen Liang, Chien-Hua Wang, Po-Ching Chou, Jong-Hau Hsu, Chia-Tsuan Huang, Yuh-Jyh Jong

    Published 2015-12-01
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  8. 8
    Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

    Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan. by Wen-Chen Liang, Xia Tian, Chung-Yee Yuo, Wan-Zi Chen, Tsu-Min Kan, Yi-Ning Su, Ichizo Nishino, Lee-Jun C Wong, Yuh-Jyh Jong

    Published 2017-01-01
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  9. 9
    Newborn screening facilitates early theranostics and improved spinal muscular atrophy outcome: five-year real-world evidence from Taiwan

    Newborn screening facilitates early theranostics and improved spinal muscular atrophy outcome: five-year real-world evidence from Taiwan by Chen-Hua Wang, Ting-Rong Hsu, Mei-Ying Liu, Li-Yun Wang, I-Jun Chou, Wang-Tso Lee, Wen-Chen Liang, Inn-Chi Lee, Hsiao-Jan Chen, Shu-Min Kao, Hui-Chen Ho, Dau-Ming Niu, Kwang-Jen Hsiao, Ming-Yuh Chang, Hui-Min Hsieh, Yuh-Jyh Jong

    Published 2025-04-01
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