Potential Harmful Effects of PM2.5 on Occurrence and Progression of Acute Coronary Syndrome: Epidemiology, Mechanisms, and Prevention Measures

by Xu Meng, Ying Zhang, Kun-Qi Yang, Yan-Kun Yang, Xian-Liang Zhou
Published 2016-07-01

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

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

by Yi-Ting Lu, Peng Fan, Di Zhang, Ying Zhang, Xu Meng, Qiong-Yu Zhang, Lin Zhao, Kun-Qi Yang, Xian-Liang Zhou
Published 2021-01-01

Gypenosides Protected the Neural Stem Cells in the Subventricular Zone of Neonatal Rats that Were Prenatally Exposed to Ethanol

by Lun Dong, Kun-Qi Yang, Wen-Yan Fu, Zhen-Hua Shang, Qing-Yu Zhang, Fang-Miao Jing, Lin-Lin Li, Hua Xin, Xiao-Jing Wang
Published 2014-11-01

Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family

by 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
Published 2019-08-01

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

Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation

by Peng Fan, Di Zhang, Xiao-Cheng Pan, Kun-Qi  Yang, Qiong-Yu Zhang, Yi-Ting Lu, Ying Zhang, Xue-Ying Liu, Wen-Jun Ma, Hui-Min Zhang, Lei Song, Jun Cai, Ya-Xin Liu, Xian-Liang Zhou
Published 2020-07-01

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

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