Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Xuguang, Qin"'
Autor:
Li Ma, Guangming Tian, Yuejin Pu, Xuguang Qin, Yinghu Zhang, Haojie Wang, Lei You, Gaofeng Zhang, Chun Fang, Xiongyan Liang, Hongbo Wei, Lei Tan, Liren Jiang
Publikováno v:
Frontiers in Microbiology, Vol 15 (2024)
IntroductionThis study aimed to assess the protective efficacy of Bacillus coagulans MF-06 as a potential alternative to antibiotics in mitigating intestinal mucosal damage in chicks infected with Salmonella pullorum.MethodsA total of 150 one-day-old
Externí odkaz:
https://doaj.org/article/22ce112c94684a8f934bbf21da8d390b
Publikováno v:
Clinical Cardiology and Cardiovascular Interventions. 4:01-09
Coronary artery anomalies (CAAs) are very rare a relatively uncommon, diverse group of congenital disorders of coronary arterial anatomy with a clinical presentations. Though most commonly detected incidentally finding during routine catheter, CT ang
Autor:
Xuguang Qin
Publikováno v:
Clinical Cardiology and Cardiovascular Interventions. 3:01-06
Congenital anomalies of coronary arteries (CAAS) are very rare and usually documented as an incidental finding during routine catheter or CT angiograms performed for other reasons. Their prevalence ranges from 0.2% to 1.3% based published series. The
Publikováno v:
Journal of Integrative Cardiology. 6
Publikováno v:
Biomedical Journal of Scientific & Technical Research. 21
Coronary artery anomalies (CAAs) are present at birth but are usually asymptomatic and are found during coronary angiography or multi-slice computed tomography (MSCT) detection.
Publikováno v:
Trends in Medicine. 18
Publikováno v:
Trends in Medicine. 18
Autor:
Xuguang Qin
Publikováno v:
Journal of the American College of Cardiology. 65(17):S457-S459
Publikováno v:
Clinical Interventions in Aging
Coronary artery anomalies (CAAs) are present at birth, but are usually asymptomatic and are found during coronary angiography or multi-slice computed tomography (MSCT) detection. The most common coronary anomaly is the separating origin of left anter
Autor:
Xin, Liu, Wenling, Liu, Dayi, Hu, Li, Zhang, Tiangang, Zhu, Cuilan, Li, Xiaoliang, Qiu, Lei, Li, Chengjun, Guo, Xingpeng, Liu, Lei, Wang, Hua, Zheng, Chunling, Wang, Qing, Diao, Dan, Shi, Pingyun, Zhan, Yuanming, Deng, Kunshen, Liu, Yi, Wang, Baomin, Liu, Hongming, Liu, Xuguang, Qin, Yanping, Lan
Publikováno v:
Zhonghua nei ke za zhi. 54(12)
The purpose of this study was to screen genetic variations in plakophilin-2 (PKP2) gene in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) and investigate the differences in clinical features between mutation and no-m