Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Xiao-Xian Tian"'
Autor:
Yun Chen, Yun-Li Lai, Yi-Ping Shen, Xiao-Xian Tian, Chen-Guang Zheng, Hong-Wei Wei, Yang Pan, Dan-Dan Shi
Publikováno v:
Maternal-Fetal Medicine, Vol 2, Iss 2, Pp 84-88 (2020)
Abstract. Objective:. To evaluate the clinical utility of noninvasive prenatal screening (NIPS) for fetuses with congenital heart disease (CHD) and impact of NIPS results on pregnancy outcome. Methods:. This was a retrospective study of pregnant wome
Externí odkaz:
https://doaj.org/article/a71a0130b05f4973883d4c3fe011d5eb
Autor:
Xi Chen, Sheng-Li Li, Guo-Yang Luo, Errol R Norwitz, Shu-Yuan Ouyang, Hua-Xuan Wen, Ying Yuan, Xiao-Xian Tian, Jia-Min He
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 8, Pp 920-928 (2017)
Background: Fetal brain development is a complicated process that continues throughout pregnancy. Fetal sulcus development has typical morphological features. Assessment of fetal sulcus development to understand the cortical maturation and developmen
Externí odkaz:
https://doaj.org/article/5b3fd3ae20c64795bca718b577ead0e7
Autor:
Yun Chen, Yun-Li Lai, Yi-Ping Shen, Xiao-Xian Tian, Chen-Guang Zheng, Hong-Wei Wei, Yang Pan, Dan-Dan Shi
Publikováno v:
Maternal-Fetal Medicine, Vol 2, Iss 2, Pp 84-88 (2020)
Objective:. To evaluate the clinical utility of noninvasive prenatal screening (NIPS) for fetuses with congenital heart disease (CHD) and impact of NIPS results on pregnancy outcome. Methods:. This was a retrospective study of pregnant women with fet
Autor:
Shuihua Yang, Zuo-jian Yang, Yu-lan Pang, Meng-feng Liang, Gui-chan Qin, Xiao-xian Tian, Xin-yan Li
Background Report a case of hypoplastic left heart syndrome (HLHS) with endomyocardial fibroelastosis (EFE) diagnosed in the first trimester. Case presentation We detected a balloon shaped left ventricle, a narrowed reverse blood stream signal in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::615cf7438f7b8aee66c37852ed9f271d
https://doi.org/10.21203/rs.3.rs-36525/v1
https://doi.org/10.21203/rs.3.rs-36525/v1
Publikováno v:
Journal of Medical Ultrasonics. 46:273-275
Persistent truncus arteriosus (PTA) is a relatively uncommon congenital heart disease, accounting for approximately 0.7-1.4% of all congenital cardiac abnormalities worldwide. PTA is usually accompanied by a single semilunar valve, with leaflets rang
Publikováno v:
Journal of Medical Ultrasonics. 44:281-287
To evaluate the accuracy of oblique view extended imaging (OVEI) in locating the position of the fetal conus medullaris. One hundred and twenty-two normal fetuses and five counterparts with spinal bifida received prenatal ultrasound examination. The
Autor:
Zuojian Yang, Shui-Hua Yang, Shengli Li, Xue-qin Li, Xiao-xian Tian, Peng-hui Luo, Xin-yan Li
Publikováno v:
Journal of medical ultrasonics (2001). 45(2)
Pulmonary atresia with ventricular septal defect (PA-VSD) is a rare complex congenital heart defect. Major artery-pulmonary collateral arteries (MAPCAs) are characteristic of PA-VSD. Prenatal diagnosis can be achieved in most cases of PA-VSD with rec
Autor:
Liang Sun, Jing Qin, Xiao-Xian Tian, Ke Chen, Chi Chen, Juan Du, Ze Yang, Chen-Guang Zheng, Lei Xiang
Publikováno v:
Hereditas (Beijing). 31:261-264
To investigate the distribution and the characteristics of karyotypes in Down syndrome patients in Nanning city, China, Cytogenetic analysis was carried out in 500 cases clinically suspected for Down syndrome during 1994 to 2007. One hundred and thir
Publikováno v:
Hereditas (Beijing). 31:142-146
To study the relationship between chromosomal abnormality and clinical ending events of reproductive abnormality, G-banding and karyotype analyses were carried out by using chromosome preparations from peripheral blood lymphocytes. Out of 5 774 cases
Autor:
Jing, Qin, Chen-Guang, Zheng, Juan, DU, Ke, Chen, Xiao-Xian, Tian, Lei, Xiang, Liang, Sun, Ze, Yang
Publikováno v:
Yi chuan = Hereditas. 31(2)
To study the relationship between chromosomal abnormality and clinical ending events of reproductive abnormality, G-banding and karyotype analyses were carried out by using chromosome preparations from peripheral blood lymphocytes. Out of 5 774 cases