Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Qi‐Xian Zeng"'
Publikováno v:
Heliyon, Vol 9, Iss 12, Pp e22570- (2023)
Background: Pulmonary artery dissection (PAD) is an uncommon condition associated with high mortality rates. To date, a comprehensive examination of various underlying causes of PAD remains unexplored. Methods: We used the search words ''pulmonary ar
Externí odkaz:
https://doaj.org/article/cb0d8029364546ecbe196c441ed0434b
Autor:
Bing-Yang Liu, Wei-Chun Wu, Qi-Xian Zeng, Zhi-Hong Liu, Li-Li Niu, Yue Tian, Qin Luo, Zhi-Hui Zhao, Rui-Lin Quan, Jing-Ru Lin, Hao Wang, Jian-Guo He, Chang-Ming Xiong
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
To investigate and compare the value of right ventricular longitudinal strain detected by two-dimensional and three-dimensional speckle-tracking echocardiography in risk stratification evaluation in pre-capillary pulmonary hypertension. We consecutiv
Externí odkaz:
https://doaj.org/article/3a4ff37642044cf8933b69576351c1d8
Autor:
Bing-yang Liu, Wei-chun Wu, Qi-xian Zeng, Zhi-hong Liu, Li-li Niu, Yue Tian, Xiao-ling Cheng, Qin Luo, Zhi-hui Zhao, Chen-hong An, Li Huang, Hao Wang, Jian-guo He, Chang-ming Xiong
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
We investigated and compared the correlations between two-dimensional speckle tracking echocardiography detected left ventricular peak early diastolic strain rates (global: left ventricular global peak early diastolic strain rate; septum: left ventri
Externí odkaz:
https://doaj.org/article/42c05e63837942a2a405eb14b3c40787
Autor:
Lin Xue, Yi‐Cheng Yang, Qing Zhao, Zhi‐Hui Zhao, Qi‐Xian Zeng, Tao Yang, Qin Luo, Bing‐Yang Liu, Xiu‐Ping Ma, Zhi‐Hong Liu, Chang‐Ming Xiong
Publikováno v:
Clin Cardiol
BACKGROUND: Arrhythmia is not uncommon among pulmonary hypertension (PH) population, and may be associated with disease severity. HYPOTHESIS: To investigate different spectrums and prevalence of arrhythmias in different clinical PH groups in Chinese
Publikováno v:
European Heart Journal - Case Reports. 6
Background Patent ductus arteriosus (PDA) can close on its own during childhood. Patent ductus arteriosus with left pulmonary artery (LPA) occlusion is rare. Here, we describe possible aetiologies of this condition and treatment strategies based on r
Publikováno v:
European Heart Journal - Case Reports. 6
Autor:
Jian-Guo He, Weichun Wu, Chang-Ming Xiong, Hao Wang, Zhihong Liu, Qin Luo, Qi-Xian Zeng, Li-Li Niu, Li Huang, Yue Tian, Xiao-Ling Cheng, Zhihui Zhao, Bing-Yang Liu
Publikováno v:
The International Journal of Cardiovascular Imaging. 35:1499-1508
Resting two-dimensional speckle tracking echocardiography (2D-STE) identified right ventricular (RV) systolic function were reported to predict exercise capacity in pulmonary hypertension (PH) patients, but little attention had been payed to 2D-STE d
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Pulmonary hypertension (PH) is defined as a mean pulmonary arterial pressure (PAP) ≥25 mm Hg measured by right heart catheterization. However, the upper limit of a normal mean PAP is 20 mm Hg. There is a gap between the upper limit of no
Autor:
Zhihong Liu, Tao Yang, Chang-Ming Xiong, Xin Li, Qi Jin, Zhihui Zhao, Qin Luo, Qing Zhao, Lu Yan, Yi Zhang, Qi-Xian Zeng
Publikováno v:
World J Clin Cases
Chronic thromboembolic pulmonary hypertension (CTEPH) is a complex chronic disease in which pulmonary artery stenosis or obstruction caused by organized thrombus can lead to increased pulmonary artery pressure and pulmonary vascular resistance, ultim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f43c6ad4e1cb6a31d122ba5fddd6b618
https://europepmc.org/articles/PMC7360712/
https://europepmc.org/articles/PMC7360712/
Autor:
Hang Yang, Chang-Ming Xiong, Yanyun Ma, Qianlong Chen, Qi-Xian Zeng, Wenke Li, Zhou Zhou, Qin Luo, Zhihong Liu, Zhihui Zhao, Bing-Yang Liu
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-8 (2020)
BMC Pulmonary Medicine
BMC Pulmonary Medicine
Background Variants in the gene encoding bone morphogenetic protein receptor type II (BMPR2) are the most common genetic cause of pulmonary arterial hypertension (PAH), whereas biallelic variants in the eukaryotic translation initiation factor 2 alph