Hasil Pencarian - Xian-liang Zhou
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Association of interleukin-18 gene polymorphisms with Takayasu arteritis in a Chinese Han population oleh Dan Wen, Xian-Liang Zhou, Xin Du, Jian-Zeng Dong, Chang-Sheng Ma, Ning-Ning Wang
Diterbitkan 2020-10-01
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Effects of dry-wet circulation on cement-based composite filling materials oleh Xian-liang ZHOU, Chang-wu LIU, Bo FENG, Bing-bing GUO, Yong-hu LU, Lian-wei ZHANG
Diterbitkan 2019-12-01
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Seasonal variation of ambulatory blood pressure in Chinese hypertensive adolescents oleh Yi Zhou, Lin Zhao, Xu Meng, Qiu-Jing Cai, Xiao-Lei Zhao, Xian-Liang Zhou, Ai-Hua Hu
Diterbitkan 2022-11-01
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Apparent mineralocorticoid excess: comprehensive overview of molecular genetics oleh Yi-ting Lu, Di Zhang, Qiong-yu Zhang, Ze-ming Zhou, Kun-qi Yang, Xian-liang Zhou, Fan Peng
Diterbitkan 2022-11-01
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Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy oleh Yan Xiao, Kun-Qi Yang, Yan-Kun Yang, Ya-Xin Liu, Tao Tian, Lei Song, Xiong-Jing Jiang, Xian-Liang Zhou
Diterbitkan 2015-01-01
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Overview of Monogenic Forms of Hypertension Combined With Hypokalemia oleh Yi-Ting Lu, Peng Fan, Di Zhang, Ying Zhang, Xu Meng, Qiong-Yu Zhang, Lin Zhao, Kun-Qi Yang, Xian-Liang Zhou
Diterbitkan 2021-01-01
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Clinical differences between small and large pheochromocytomas and paragangliomas oleh Lin Zhao, ZhiMao Li, Xu Meng, Hua Fan, ZengLei Zhang, ZhaoCai Zhang, YeCheng Liu, XianLiang Zhou, HuaDong Zhu
Diterbitkan 2023-03-01
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Clinical characteristics of concurrent primary aldosteronism and renal artery stenosis: A retrospective case–control study oleh Xu Meng, Yan-Kun Yang, Yue-Hua Li, Peng Fan, Ying Zhang, Kun-Qi Yang, Hai-Ying Wu, Xiong-Jing Jiang, Jun Cai, Xian-Liang Zhou
Diterbitkan 2021-01-01
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A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension oleh Yi-Ting Lu, Xin-Chang Liu, Ze-Ming Zhou, Di Zhang, Lin Sun, Ying Zhang, Peng Fan, Lin Zhang, Ya-Xin Liu, Fang Luo, Xian-Liang Zhou
Diterbitkan 2022-06-01
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Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family oleh Peng Fan, Chao-Xia Lu, Kun-Qi Yang, Pei-Pei Lu, Su-Fang Hao, Fang Luo, Hui-Min Zhang, Lei Song, Hai-Ying Wu, Jun Cai, Xue Zhang, Xian-Liang Zhou
Diterbitkan 2019-08-01
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A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation oleh 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
Diterbitkan 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 oleh 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
Diterbitkan 2022-05-01
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Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome oleh 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
Diterbitkan 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 oleh 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
Diterbitkan 2022-06-01
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