Zobrazeno 1 - 10
of 108
pro vyhledávání: '"XIAN-LIANG ZHOU"'
Autor:
Yi Zhou, Lin Zhao, Zenglei Zhang, Xu Meng, Qiu-jing Cai, Xiao-lei Zhao, Lin-ping Wang, Ai-hua Hu, Xian-liang Zhou
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background For adolescents, abnormal dipping patterns in blood pressure (BP) are associated with early-onset organ damage and a higher risk of cardiovascular disorders in adulthood. Obesity is one of the most common reasons for abnormal BP d
Externí odkaz:
https://doaj.org/article/3b0543d327774282b40f503b7cc25960
Autor:
Yi-Ting Lu, Zeng-Lei Zhang, Xing-Yu Zhou, Di Zhang, Tao Tian, Peng Fan, Ying Zhang, Xian-Liang Zhou
Publikováno v:
iScience, Vol 26, Iss 12, Pp 108421- (2023)
Summary: Few models exist for predicting severe ischemic complications (SIC) in patients with Takayasu arteritis (TA). We conducted a retrospective analysis of 703 patients with TA from January 2010 to December 2019 to establish an SIC prediction mod
Externí odkaz:
https://doaj.org/article/3e15428364734307bb9c809a0a44e562
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-16 (2022)
Abstract Apparent mineralocorticoid excess is an autosomal recessive form of monogenic disease characterized by juvenile resistant low-renin hypertension, marked hypokalemic alkalosis, low aldosterone levels, and high ratios of cortisol to cortisone
Externí odkaz:
https://doaj.org/article/7a1fa2d163984536b6dfab7bd4683c8c
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundBlood pressure (BP) exhibits seasonal variation with lower levels at higher temperatures and vice versa. This phenomenon affects both sexes and all age groups. So far, only a few research studies have investigated this condition in adolesce
Externí odkaz:
https://doaj.org/article/6cb6eae2deb04abb9aabafa111f0cd97
Autor:
Yi-Ting Lu, Buweimairemu Rejiepu, Di Zhang, Dong-Cheng Cai, Kun-Qi Yang, Tao Tian, Xian-Liang Zhou, Peng Fan
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-1 (2023)
Introduction: Neurofibromatosis type 1 (NF-1) is caused by mutations in the NF1 gene that encodes neurofibromin, a negative regulator of RAS proto-oncogene. Approximately one-third of the reported pathogenic mutations in NF1 are splicing mutations, b
Externí odkaz:
https://doaj.org/article/400f8740c54d404493e6b3c71fe31273
Autor:
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
Publikováno v:
Clinical and Experimental Hypertension, Vol 43, Iss 1, Pp 7-12 (2021)
Background: Rare cases of concurrent primary aldosteronism (PA) and renal artery stenosis (RAS) have been reported. Methods: In this retrospective case–control study, we selected a cohort of 10 PA with RAS patients and a control group of 20 PA with
Externí odkaz:
https://doaj.org/article/dbb1fddedd334860a5c519b3fd54cc8d
Autor:
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
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Externí odkaz:
https://doaj.org/article/ea37c960bdf945ca81cceb92933d60c3
Autor:
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
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
BackgroundLiddle syndrome is a form of monogenic hypertension caused by mutations in the three homologous subunits of the epithelial sodium channels (ENaCs), α, β, and γ. It is characterized by early-onset refractory hypertension, hypokalemia, low
Externí odkaz:
https://doaj.org/article/59143b1187f544ca81a2d52236f202aa
Autor:
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
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveLiddle syndrome (LS) is a monogenic hypertension consistent with autosomal dominant inheritance, often with early onset high blood pressure in childhood or adolescence. This study aimed to identify the pathogenicity of a nonsense mutation in
Externí odkaz:
https://doaj.org/article/6a3dc85f7de845fbbd633bcff907473f
Association of interleukin-18 gene polymorphisms with Takayasu arteritis in a Chinese Han population
Publikováno v:
Chinese Medical Journal, Vol 133, Iss 19, Pp 2315-2320 (2020)
Abstract. Background:. Interleukin-18 (IL18) gene polymorphisms are related to many inflammatory and autoimmune diseases. However, a correlation analysis between IL18 −607C/A and −137G/C gene polymorphisms and Takayasu arteritis (TA) is lacking.
Externí odkaz:
https://doaj.org/article/12a0ecad4934483e8df7d70d0d493843