Search Results - Wong, Swee-Hee

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  1. 1
    Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes

    Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes by Lee, Inn-Chi, Yang, Jiann-Jou, Wong, Swee-Hee, Liou, Ying-Ming, Li, Shuan-Yow

    Published in Scientific reports
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  2. 2
    KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders

    KCNQ2 Selectivity Filter Mutations Cause Kv7.2 M-Current Dysfunction and Configuration Changes Manifesting as Epileptic Encephalopathies and Autistic Spectrum Disorders by Lee, Inn-Chi, Yang, Jiann-Jou, Liou, Ying-Ming, Wong, Swee-Hee

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  3. 3
    Early Biomarkers and Hearing Impairments in Patients with Neonatal Hypoxic–Ischemic Encephalopathy

    Early Biomarkers and Hearing Impairments in Patients with Neonatal Hypoxic–Ischemic Encephalopathy by Chen, Da-Yang, Lee, Inn-Chi, Wang, Xing-An, Wong, Swee-Hee

    Published in Diagnostics (Basel)
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  4. 4
    KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization

    KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization by Wong, Swee-Hee, Liou, Ying-Ming, Yang, Jiann-Jou, Lee, Inn-Chi

    Published in Epilepsy & behavior
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  5. 5
    Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy

    Identifying Early Diagnostic Biomarkers Associated with Neonatal Hypoxic-Ischemic Encephalopathy by Lee, Inn-Chi, Wong, Swee-Hee, Wang, Xing-An, Yu, Chin-Sheng

    Published in Diagnostics (Basel)
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  6. 6
    Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl

    Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl by Wu, Shey‐Lin, Tsai, Ming‐Shiun, Wong, Swee‐Hee, Hsieh‐Li, Hsiu‐Mei, Tsai, Tz‐Shiu, Chang, Wei‐Tang, Huang, Shin‐Ling, Chiu, Chun‐Ching, Wang, Sue‐Hong

    Published in Developmental dynamics
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  7. 7
    Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss

    Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss by Wong, Swee-Hee, Yen, Yung-Chang, Li, Shuan-Yow, Yang, Jiann-Jou

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  8. 8
    Troponin I Levels in Neonatal Hypoxic-Ischemic Encephalopathy Are Related to Cardiopulmonary Comorbidity and Neurodevelopmental Outcomes

    Troponin I Levels in Neonatal Hypoxic-Ischemic Encephalopathy Are Related to Cardiopulmonary Comorbidity and Neurodevelopmental Outcomes by Lee, Inn-Chi, Yu, Chin-Sheng, Wong, Swee-Hee, Lue, Ko-Huang

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  9. 9
    Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene

    Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene by Wong, Swee-Hee, Wang, Wen-Hung, Chen, Pin-Hua, Li, Shuan-Yow, Yang, Jiann-Jou

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