Zobrazeno 1 - 10
of 2 001
pro vyhledávání: '"Interrupted aortic arch"'
Publikováno v:
European Journal of Medical Research, Vol 28, Iss 1, Pp 1-11 (2023)
Abstract Background Acute renal injury (AKI) after aortic arch reconstruction with cardiopulmonary bypass leads to injury of multiple organs and increases perioperative mortality. The study was performed to explore risk factors for AKI. We aim to dev
Externí odkaz:
https://doaj.org/article/1a27c29c85e940ecb30d1a1489bb005b
Autor:
Christina L. Greene, MD, Brandi Scully, MD, Steven J. Staffa, MS, Mariana Chavez, MD, Kevin G. Friedman, MD, Pedro del Nido, MD, Luis G. Quinonez, MD, Sitaram M. Emani, MD, Christopher W. Baird, MD
Publikováno v:
JTCVS Open, Vol 15, Iss , Pp 361-367 (2023)
Objective: The Yasui operation was introduced in 1987 for patients with 2 adequate ventricles, a ventricular septal defect, and aortic atresia or interrupted aortic arch. Despite promising early outcomes, left ventricular outflow tract obstruction (L
Externí odkaz:
https://doaj.org/article/5ebc2a9a636f42a981fa011e654e55c1
Publikováno v:
International Journal of General Medicine, Vol Volume 16, Pp 3229-3245 (2023)
Peng An,1,2,* Lina Song,1,* Ping Song,3,* Junyan Zhang,1,3 Yong Lin,1,3 Guoyan Feng,1 Junjie Liu3 1Department of Radiology, Xiangyang No.1 People’s Hospital, Hubei University of Medicine, Xiangyang, 441000, People’s Republic of China;
Externí odkaz:
https://doaj.org/article/07ee204da26b452f8ddaa98ead67940d
Autor:
Giuseppe Vadalà
Publikováno v:
Euromediterranean Biomedical Journal, Vol 18, Iss 33, Pp 160-161 (2023)
Interrupted Aortic Arch (IAA) is a rare congenital abnormality characterized by a complete discontinuity of the aortic lumen, usually located after the origin of the left subclavian artery. IAA is mainly diagnosed during childhood and has an extremel
Externí odkaz:
https://doaj.org/article/561890f9498042a792b601f8fb94c21e
Autor:
Kevin Moses Hanky Jr Tandayu, Yovi Kurniawati, Indriwanto Sakidjan Atmosudigdo, Oktavia Lilyasari
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 5, Pp 374-377 (2023)
Berry syndrome is an extremely rare constellation of several congenital cardiac anomalies consisting of aortopulmonary window, aortic origin of the right pulmonary artery (AORPA), interrupted aortic arch or hypoplastic aortic arch or coarctation of t
Externí odkaz:
https://doaj.org/article/a1b91240bf6343e98a047504a47b82da
Autor:
Archita Goel, Sanjaya Viswamitra
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 32, Iss 03, Pp 372-380 (2022)
Aortic abnormalities account for 15 to 20% of all congenital cardiovascular diseases. The purpose of this pictorial essay is to illustrate various congenital anomalies of the aortic arch, which influence patient management and outcome.
Externí odkaz:
https://doaj.org/article/4813010927444e768fb52d8d86575156
Publikováno v:
Romanian Journal of Pediatrics, Vol 71, Iss 2, Pp 73-76 (2022)
Interrupted aortic arch is a rare ductal-dependent congenital heart malformation, accounting for 1.5% of all MCC, 2 in 100,000 cases of live newborns are diagnosed with IAA. We present the case of a 3-month-old infant who came to our clinic on the re
Externí odkaz:
https://doaj.org/article/3b7f8241bfd8487cb336e4900eb67323
Publikováno v:
Asian Journal of Surgery, Vol 46, Iss 7, Pp 2948-2949 (2023)
Externí odkaz:
https://doaj.org/article/b1a796f374c444879a1e0d9a651dceeb
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Akademický článek
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