Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Aortic Valve Atresia"'
OBJECTIVES To analyze near-term cerebroplacental Doppler, heart morphology, and neonatal biometry in isolated hypoplastic left heart syndrome (HLHS) relative to healthy controls. METHODS This retrospective study included 55 fetuses with HLHS (29 with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a50dda1ab70a4639e9b069b35d4fc7
https://ruj.uj.edu.pl/xmlui/handle/item/285619
https://ruj.uj.edu.pl/xmlui/handle/item/285619
Publikováno v:
Cardiology in the young. 30(11)
A combination of aortic valve atresia and an interrupted aortic arch is a unique disease in which perfusion to the brain and myocardium depends on coexisting lesions or type of interruption. We report a case of aortic valve atresia with type B interr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e273f5fbc1bb3f4bdc7c3003907cc4
https://pubmed.ncbi.nlm.nih.gov/33198834
https://pubmed.ncbi.nlm.nih.gov/33198834
Autor:
Tara Karamlou, James K. Kirklin, James M. Meza, Brian W. McCrindle, Kamal Pourmoghadam, Pirooz Eghtesady, Eugene H. Blackstone, Martijn G. Slieker, Richard W. Kim, Mohsen Karimi, Phillip T. Burch, Luc Mertens, William M. DeCampli, Marshall L. Jacobs
Publikováno v:
Computer Methods and Programs in Biomedicine, 165, pp. 107-116
Computer Methods and Programs in Biomedicine, 165, 107-116
Computer Methods and Programs in Biomedicine, 165, 107-116
Background Qualitative features of aortic and mitral valvar pathology have traditionally been used to classify congenital cardiac anomalies for which the left heart structures are unable to sustain adequate systemic cardiac output. We aimed to determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::806d5d95ac26af64935a440ee9214b4b
https://doi.org/10.1016/j.cmpb.2018.08.014
https://doi.org/10.1016/j.cmpb.2018.08.014
Autor:
James K. Kirklin, Marshall L. Jacobs, Eugene H. Blackstone, Brian W. McCrindle, Kathryn A. Stackhouse, Christo I. Tchervenkov, Gösta B. Pettersson, Jeevanantham Rajeswaran, Jeffrey P. Jacobs, Leonard L. Bailey
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 159:1451-1461.e7
Objective The study objective was to describe the surgical pathway progression through adolescence of an inception cohort of neonates with aortic valve atresia managed initially with surgical palliation or primary transplantation, comparing survival
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20c223712a36ce53f5f5e023fdc540d7
https://doi.org/10.1016/j.jtcvs.2019.08.104
https://doi.org/10.1016/j.jtcvs.2019.08.104
Autor:
Brian C. Guenther, Jonathan Dayan
Publikováno v:
Journal of Echocardiography. 18:75-76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a47203ec0f467675a60775b358dbadc0
https://doi.org/10.1007/s12574-018-0414-4
https://doi.org/10.1007/s12574-018-0414-4
Publikováno v:
Cardiology in the Young. 25:1193-1196
A 20-day-old girl was referred to our clinic for systolic murmur, cyanosis, and dyspnoea with feeding. Echocardiography revealed an atretic aortic valve. CT angiography scan revealed that the left common carotid artery originated from the distal main
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e13cd1df251b33f06cb2d222e2f0d6
https://doi.org/10.1017/s1047951115000475
https://doi.org/10.1017/s1047951115000475
Publikováno v:
The Thoracic and Cardiovascular Surgeon. 63:354-359
BACKGROUND Restrictive atrial septal defect (ASD) is described as risk factor for Norwood procedure because of elevated pulmonary resistance. We hypothesized that it invariably could not cause pulmonary hypertension, unless it was combined with mitra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d27a477793bffc825042acfd2dc7ae5e
https://doi.org/10.1055/s-0034-1374060
https://doi.org/10.1055/s-0034-1374060
Publikováno v:
Catheterization and Cardiovascular Interventions. 84:1157-1162
We report an infant with aortic valve atresia, interrupted aortic arch, ventricular septal defect, confluent pulmonary arteries, bilateral arterial ducts, absent common carotid arteries, and anomalous coronary arteries arising from main pulmonary art
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::119811cf37314d73471d790dc2232b71
https://doi.org/10.1002/ccd.25424
https://doi.org/10.1002/ccd.25424
Publikováno v:
Journal of Diagnostic Medical Sonography. 28:299-302
This case study describes a newborn male infant with cat eye syndrome, found to have a rare constellation of congenital defects, which included an interrupted aortic arch, type B2 (with aberrant right subclavian artery), aortic valve atresia, aorto-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1776127499394ac10fda373de887bfc
https://doi.org/10.1177/8756479312455862
https://doi.org/10.1177/8756479312455862
Autor:
Angelo S. Milazzo, Ronald J. Kanter, Margaret L. Kirby, Donald P. Frush, Carissa M. Baker-Smith, James Jaggers, Piers Barker
Publikováno v:
Congenital Heart Disease. 5:316-320
Aortic valve atresia with interruption of the aortic arch is an extremely rare anomaly; only eleven cases of this anomaly have been reported to date. In the absence of additional sources of blood flow to the ascending aorta, aortic valve atresia with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0811f2339ef6c7168bb8c6d9c8f7680
https://doi.org/10.1111/j.1747-0803.2009.00341.x
https://doi.org/10.1111/j.1747-0803.2009.00341.x