Search Results - "Nápoli, Natalia"
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Fetal aortic valvuloplasty as the first step in a complex therapeutic strategy
Published in Prenatal diagnosis (01-06-2024)“…Background Fetal aortic valvuloplasty (FAV) is proposed to prevent hypoplastic left heart syndrome due to fetal critical aortic stenosis. Objective: to report…”
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Prenatal diagnosis of idiopathic dilatation of the right atrium. A case report
Published in Archivos argentinos de pediatría (01-12-2020)Get full text
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Health related quality of life in children with congenital heart disease that undergo cardiac surgery during their first year of life
Published in Archivos argentinos de pediatría (01-06-2020)“…Advances in diagnostic methods, surgical techniques and postoperative intensive care have significantly increased the survival rates for children with…”
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Anomalous origin of the right coronary artery from the pulmonary artery in an infant with a heart murmur: Case report
Published in Archivos argentinos de pediatría (01-12-2018)“…The anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a rare entity that has an incidence of 0.002 % and can potentially…”
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Novel use of reverse double switch operation in failed left ventricular recruitment pathway
Published in Interactive cardiovascular and thoracic surgery (03-08-2022)“…Abstract In spite of great advances in staged left ventricle recruitment strategy, some patients do not achieve biventricular circulation nor are candidates…”
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Cover Image
Published in Prenatal diagnosis (01-06-2024)“…The cover image is based on the Original Article Fetal aortic valvuloplasty as the first step in a complex therapeutic strategy by Sofía Grinenco et al.,…”
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Oiigen anomalo de la arteria coronaiia derecha de la arteiia pulmonar en un lactante con soplo cardiaco: A proposito de un caso
Published in Archivos argentinos de pediatría (01-12-2018)“…El origen anómalo de la arteria coronaria derecha de la arteria pulmonar es una entidad rara con una incidencia del 0,002 % y potencialmente grave, que puede…”
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Loeys-Dietz Syndrome, 3 generations, 4 familial cases
Published in Archivos argentinos de pediatría (01-08-2017)“…Loeys-Dietz Syndrome is an autosomal dominant disease with aortic aneurysms, arterial tortuosity with hypertelorism and bifid uvula. We describe four familial…”
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Síndrome de Loeys-Dietz, 3 generaciones, 4 casos familiares
Published in Archivos argentinos de pediatría (01-08-2017)“…El síndrome de Loeys-Dietz es una enfermedad genética autosómica dominante caracterizada por aneurismas aórticos, tortuosidad arterial generalizada,…”
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