Association of interleukin-18 gene polymorphisms with Takayasu arteritis in a Chinese Han population by Dan Wen, Xian-Liang Zhou, Xin Du, Jian-Zeng Dong, Chang-Sheng Ma, Ning-Ning Wang

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Seasonal variation of ambulatory blood pressure in Chinese hypertensive adolescents by Yi Zhou, Lin Zhao, Xu Meng, Qiu-Jing Cai, Xiao-Lei Zhao, Xian-Liang Zhou, Ai-Hua Hu

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Apparent mineralocorticoid excess: comprehensive overview of molecular genetics by Yi-ting Lu, Di Zhang, Qiong-yu Zhang, Ze-ming Zhou, Kun-qi Yang, Xian-liang Zhou, Fan Peng

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Predicting stroke and myocardial infarction risk in Takayasu arteritis with automated machine learning models by Yi-Ting Lu, Zeng-Lei Zhang, Xing-Yu Zhou, Di Zhang, Tao Tian, Peng Fan, Ying Zhang, Xian-Liang Zhou

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Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing NF1 Mutation by Yi-Ting Lu, Buweimairemu Rejiepu, Di Zhang, Dong-Cheng Cai, Kun-Qi Yang, Tao Tian, Xian-Liang Zhou, Peng Fan

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<i>RET</i> c.1901G>A and Novel <i>SLC12A3</i> Mutations in Familial Pheochromocytomas by Lin Zhao, Kun-Qi Yang, Peng Fan, Ding-Xu Gong, Lin Zhang, Yi-Ting Lu, Xu Meng, Xian-Liang Zhou

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Risk Factors for Cardiac Complications in Patients With Pheochromocytoma and Paraganglioma: A Retrospective Single-Center Study by Lin Zhao, Xu Meng, QiMin Mei, Hua Fan, YeCheng Liu, XianLiang Zhou, HuaDong Zhu, ShuYang Zhang

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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

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Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension by Yi-Ting Lu, Di Zhang, Xin-Chang Liu, Qiong-Yu Zhang, Xue-Qi Dong, Peng Fan, Yan Xiao, Xian-Liang Zhou

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Percutaneous Transluminal Renal Angioplasty for Fibromuscular Dysplasia and Prognostic Risk Factors: A Retrospective Chinese Cohort Study by Yi-Ting Lu, Ze-Ming Zhou, Di Zhang, Lin Sun, Xin-Chang Liu, Yan-Kun Yang, Xiong-Jing Jiang, Xian-Liang Zhou

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Lipoprotein(a) is a new prognostic factor in patients with psoriasis and coronary artery disease: a retrospective cohort study by Lin Zhao, Lin Sun, ZengLei Zhang, KunQi Yang, ZuoZhi Li, Man Wang, Yan Zeng, XianLiang Zhou, WeiXian Yang

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Clinical differences between small and large pheochromocytomas and paragangliomas by Lin Zhao, ZhiMao Li, Xu Meng, Hua Fan, ZengLei Zhang, ZhaoCai Zhang, YeCheng Liu, XianLiang Zhou, HuaDong Zhu

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Clinical characteristics of concurrent primary aldosteronism and renal artery stenosis: A retrospective case–control study by 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

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A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension by 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

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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

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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

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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

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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

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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

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Single Nucleotide Polymorphism rs10919543 in FCGR2A/FCGR3A Region Confers Susceptibility to Takayasu Arteritis in Chinese Population by Fang Qin, Hu Wang, Lei Song, Xi-Li Lu, Li-Rui Yang, Er-Peng Liang, Wei Wang, Yu-Bao Zou, Jin Bian, Hai-Ying Wu, Xian-Liang Zhou, Ru-Tai Hui, Hui-Min Zhang, Xiong-Jing Jiang

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