Potential Harmful Effects of PM(2.5) on Occurrence and Progression of Acute Coronary Syndrome: Epidemiology, Mechanisms, and Prevention Measures

por Meng, Xu, Zhang, Ying, Yang, Kun-Qi, Yang, Yan-Kun, Zhou, Xian-Liang
Publicado 2016

Apparent mineralocorticoid excess: comprehensive overview of molecular genetics

por Lu, Yi-ting, Zhang, Di, Zhang, Qiong-yu, Zhou, Ze-ming, Yang, Kun-qi, Zhou, Xian-liang, Peng, Fan
Publicado 2022

Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation

por Lu, Yi-Ting, Rejiepu, Buweimairemu, Zhang, Di, Cai, Dong-Cheng, Yang, Kun-Qi, Tian, Tao, Zhou, Xian-Liang, Fan, Peng
Publicado 2023

Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report

por Fan, Peng, Zhang, Di, Yang, Kun-Qi, Tian, Tao, Luo, Fang, Liu, Ya-Xin, Wang, Lin-Ping, Zhou, Xian-Liang
Publicado 2020

RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas

por Zhao, Lin, Yang, Kun-Qi, Fan, Peng, Gong, Ding-Xu, Zhang, Lin, Lu, Yi-Ting, Meng, Xu, Zhou, Xian-Liang
Publicado 2022

Clinical Characteristics and Prognosis of End-stage Hypertrophic Cardiomyopathy

por Xiao, Yan, Yang, Kun-Qi, Yang, Yan-Kun, Liu, Ya-Xin, Tian, Tao, Song, Lei, Jiang, Xiong-Jing, Zhou, Xian-Liang
Publicado 2015

Clinical characteristics and outcomes of left ventricular pseudoaneurysm: A retrospective study in a single-center of China

por Meng, Xu, Yang, Yan-Kun, Yang, Kun-Qi, Zhang, Ying, Lu, Pei-Pei, Fan, Peng, Ma, Li-Hong, Zhou, Xian-Liang
Publicado 2017

Overview of Monogenic Forms of Hypertension Combined With Hypokalemia

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

Lipoprotein(a) is a new prognostic factor in patients with psoriasis and coronary artery disease: a retrospective cohort study

por Zhao, Lin, Sun, Lin, Zhang, ZengLei, Yang, KunQi, Li, ZuoZhi, Wang, Man, Zeng, Yan, Zhou, XianLiang, Yang, WeiXian
Publicado 2023

Fibrinogen is Associated with Clinical Adverse Events in Patients with Psoriasis and Coronary Artery Disease

por Zhao, Lin, Zeng, Yan, Sun, Lin, Zhang, ZengLei, Yang, KunQi, Li, ZuoZhi, Wang, Man, Zhou, XianLiang, Yang, WeiXian
Publicado 2023

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

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

Xinfuli improves cardiac function, histopathological changes and attenuate cardiomyocyte apoptosis in rats with doxorubicin-induced cardiotoxicity

por Lu, Pei-Pei, Ma, Jie, Liang, Xiao-Peng, Guo, Cai-Xia, Yang, Yan-Kun, Yang, Kun-Qi, Shen, Qi-Ming, Ma, Li-Hong, Zhou, Xian-Liang
Publicado 2016

Prognostic value of plasma big endothelin-1 in left ventricular non-compaction cardiomyopathy

por Fan, Peng, Zhang, Ying, Lu, Yi-Ting, Yang, Kun-Qi, Lu, Pei-Pei, Zhang, Qiong-Yu, Luo, Fang, Lin, Ya-Hui, Zhou, Xian-Liang, Tian, Tao
Publicado 2021

A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation

por Yang, Kun-Qi, Lu, Chao-Xia, Zhang, Ying, Yang, Yan-Kun, Li, Jia-Cheng, Lan, Tian, Meng, Xu, Fan, Peng, Tian, Tao, Wang, Lin-Ping, Liu, Ya-Xin, Zhang, Xue, Zhou, Xian-Liang
Publicado 2017

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

por Zhang, Di, Qu, Yi, Dong, Xue-Qi, Lu, Yi-Ting, Yang, Kun-Qi, Liu, Xin-Chang, Fan, Peng, Hu, Yu-Xiao, Yang, Chun-Xue, Gao, Ling-Gen, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2022

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

por Zhang, Di, Qu, Yi, Dong, Xue-Qi, Lu, Yi-Ting, Yang, Kun-Qi, Liu, Xin-Chang, Fan, Peng, Hu, Yu-Xiao, Yang, Chun-Xue, Gao, Ling-Gen, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2022

A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia

por Fan, Peng, Zhao, Yu-Mo, Zhang, Di, Liao, Ying, Yang, Kun-Qi, Tian, Tao, Lou, Ying, Luo, Fang, Ma, Wen-Jun, Zhang, Hui-Min, Song, Lei, Cai, Jun, Liu, Ya-Xin, Zhou, Xian-Liang
Publicado 2019

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension

por Fan, Peng, Pan, Xiao-Cheng, Zhang, Di, Yang, Kun-Qi, Zhang, Ying, Tian, Tao, Luo, Fang, Ma, Wen-Jun, Liu, Ya-Xin, Wang, Lin-Ping, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhou, Xian-Liang
Publicado 2020

Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B

por Fan, Peng, Lu, Chao-Xia, Zhang, Di, Yang, Kun-Qi, Lu, Pei-Pei, Zhang, Ying, Meng, Xu, Hao, Su-Fang, Luo, Fang, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Cai, Jun, Zhang, Xue, Zhou, Xian-Liang
Publicado 2018

Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2 and characterized by early-onset hypertension and hypokalemia

por Fan, Peng, Lu, Yi-Ting, Yang, Kun-Qi, Zhang, Di, Liu, Xue-Ying, Tian, Tao, Luo, Fang, Wang, Lin-Ping, Ma, Wen-Jun, Liu, Ya-Xin, Zhang, Hui-Min, Song, Lei, Cai, Jun, Lou, Ying, Zhou, Xian-Liang
Publicado 2020