Showing 1 - 11 results of 11 for search 'Ya-Xin Liu', query time: 0.05s
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Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy by Yan Xiao, Kun-Qi Yang, Yan-Kun Yang, Ya-Xin Liu, Tao Tian, Lei Song, Xiong-Jing Jiang, Xian-Liang Zhou
Published 2015-01-01
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A Human Health Risk Assessment of Trace Elements Present in Chinese Wine by Zhi-Hao Deng, Ang Zhang, Zhi-Wei Yang, Ya-Li Zhong, Jian Mu, Fei Wang, Ya-Xin Liu, Jin-Jie Zhang, Yu-Lin Fang
Published 2019-01-01
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A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation by Kun-Qi Yang, Chao-Xia Lu, Ying Zhang, Yan-Kun Yang, Jia-Cheng Li, Tian Lan, Xu Meng, Peng Fan, Tao Tian, Lin-Ping Wang, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou
Published 2017-05-01
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Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family by Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou
Published 2022-05-01
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Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome by Kun-Qi Yang, Chao-Xia Lu, Peng Fan, Ying Zhang, Xu Meng, Xue-Qi Dong, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Hai-Ying Wu, Jun Cai, Xue Zhang, Xian-Liang Zhou
Published 2018-02-01
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Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family by Di Zhang, Yi Qu, Xue-Qi Dong, Yi-Ting Lu, Kun-Qi Yang, Xin-Chang Liu, Peng Fan, Yu-Xiao Hu, Chun-Xue Yang, Ling-Gen Gao, Ya-Xin Liu, Xian-Liang Zhou
Published 2022-06-01
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Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B by Peng Fan, Chao-Xia Lu, Di Zhang, Kun-Qi Yang, Pei-Pei Lu, Ying Zhang, Xu Meng, Su-Fang Hao, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Lei Song, Jun Cai, Xue Zhang, Xian-Liang Zhou
Published 2018-12-01
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Efficient Photocatalytic Hydrogen Evolution over TiO<sub>2-X</sub> Mesoporous Spheres-ZnO Nanorods Heterojunction by BingKe Zhang, Qi Li, Dongbo Wang, Jinzhong Wang, Baojiang Jiang, Shujie Jiao, DongHao Liu, Zhi Zeng, ChenChen Zhao, YaXin Liu, ZhiKun Xun, Xuan Fang, ShiYong Gao, Yong Zhang, LianCheng Zhao
Published 2020-10-01
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A novel phenotype with splicing mutation identified in a Chinese family with desminopathy by Peng Fan, Chao-Xia Lu, Xue-Qi Dong, Di Zhu, Kun-Qi Yang, Ke-Qiang Liu, Di Zhang, Ying Zhang, Xu Meng, Hui-Qiong Tan, Li-Tian Yu, Ke-Fei Dou, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou, Yi Cui
Published 2019-01-01
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