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pro vyhledávání: '"Sanfui Yong"'
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Right aortic arch (RAA) and retro-aortic innominate vein are rare vascular anomalies. Diagnosis of these anatomical variations can be achieved using fetal echocardiography, post-natal echocardiography, and computed tomography scan. RAA can form a vas
Externí odkaz:
https://doaj.org/article/b4d869d5ef5043f0b13dc3fed8973fc0
Publikováno v:
Cardiology in the young.
Introduction: The association of a univentricular heart defect with common arterial trunk is extremely rare. There is a lack of population-based outcome studies reported in the literature. Methods: The hospital records, echocardiographic and other im
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 11:229-231
In patients with transposition, a right aortic arch has rarely been reported among the associated malformations. When present, the arch has been obstructed because of the presence of aortic coarctation and/or arch hypoplasia. A bicuspid aortic valve
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Frontiers in Pediatrics
Frontiers in Pediatrics
Right aortic arch (RAA) and retro-aortic innominate vein are rare vascular anomalies. Diagnosis of these anatomical variations can be achieved using fetal echocardiography, post-natal echocardiography, and computed tomography scan. RAA can form a vas
Autor:
Bentham, James R., Zava, Ngoni K., Harrison, Wendy J., Shauq, Arjamand, Kalantre, Atul, Derrick, Graham, Chen, Robin H., Dhillon, Rami, Taliotis, Demetris, Sok-Leng Kang, Crossland, David, Akintayo Adesokan, Hermuz, Anthony, Kudumula, Vikram, Sanfui Yong, Noonan, Patrick, Hayes, Nicholas, Stumper, Oliver, Thomson, John D.R., Kang, Sok-Leng
Publikováno v:
Circulation; 2/6/2018, Vol. 137 Issue 6, p581-588, 8p