Works matching AU Yang, Xiaoling


Results: 249
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    Phenotypes of GNAO1 Variants in a Chinese Cohort.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.662162
    By:
    • Yang, Xiaoling;
    • Niu, Xueyang;
    • Yang, Ying;
    • Cheng, Miaomiao;
    • Zhang, Jing;
    • Chen, Jiaoyang;
    • Yang, Zhixian;
    • Zhang, Yuehua
    Publication type:
    Article
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    DYNC1H1‐related epilepsy: Genotype–phenotype correlation.

    Published in:
    Developmental Medicine & Child Neurology, 2023, v. 65, n. 4, p. 534, doi. 10.1111/dmcn.15414
    By:
    • Liu, Wenwei;
    • Cheng, Miaomiao;
    • Zhu, Ying;
    • Chen, Yi;
    • Yang, Ying;
    • Chen, Hui;
    • Niu, Xueyang;
    • Tian, Xiaojuan;
    • Yang, Xiaoling;
    • Zhang, Yuehua
    Publication type:
    Article
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    CHD2‐related epilepsy: novel mutations and new phenotypes.

    Published in:
    Developmental Medicine & Child Neurology, 2020, v. 62, n. 5, p. 647, doi. 10.1111/dmcn.14367
    By:
    • Chen, Jiaoyang;
    • Zhang, Jing;
    • Liu, Aijie;
    • Zhang, Liping;
    • Li, Hua;
    • Zeng, Qi;
    • Yang, Zhixian;
    • Yang, Xiaoling;
    • Wu, Xiru;
    • Zhang, Yuehua
    Publication type:
    Article
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    Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene <italic>WDR45</italic>.

    Published in:
    Epilepsia (Series 4), 2018, v. 59, n. 1, p. e5, doi. 10.1111/epi.13957
    By:
    • Carvill, Gemma L.;
    • Liu, Aijie;
    • Zhang, Jing;
    • Yang, Xiaoling;
    • Zhang, Yue‐Hua;
    • Mandelstam, Simone;
    • Scheffer, Ingrid E.;
    • Mackay, Mark;
    • Schneider, Amy;
    • McMahon, Jacinta M.;
    • Lacroix, Amy;
    • Zemel, Matthew;
    • Mefford, Heather C.;
    • Bello‐Espinosa, Luis;
    • Wallace, Geoffrey;
    • Waak, Michaela;
    • Malone, Stephen
    Publication type:
    Article
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