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of 59
pro vyhledávání: '"Aaron R. Levin"'
Clearly, computer-based digital subtraction offers several advantages over conventional approaches to contrast angiography. Using the newer method, in many situations contrast loads can be beneficially reduced, radiation exposure can be markedly dimi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::947b444dec20938d34e01194d97d4b2a
https://doi.org/10.1159/000410755
https://doi.org/10.1159/000410755
Autor:
Aaron R. Levin
Publikováno v:
Pediatric annals. 4(10)
Autor:
Arthur A. Klein, Frank Moran, Aaron R. Levin, Jeffrey P. Gold, Mary Allen Engle, Kathryn H. Ehlers, Kimon Violaris, Michael S. Snyder, Daniel S. Notterman, O. Wayne Isom, Samuel J. Lang, Nunzia Fatica, John E. O'Loughlin
Publikováno v:
Journal of Cardiac Surgery. 8:9-17
In spite of recent advances in neonatal open repair for complex cyanotic heart disease, some patients require palliation with a systemic-to-pulmonary artery shunt. We report a 5-year experience (1985–1990) with 112 Blalock-Taussig shunts. Forty-six
Autor:
John E. O'Loughlin, Mary T. Donofrio, Mary Allen Engle, Kathryn H. Ehlers, Michael S. Snyder, Jeffrey P. Gold, Aaron R. Levin
Publikováno v:
Journal of the American College of Cardiology. 20(2):366-372
Objectives and Background. Congenital aortic regurgitation is rare as an isolated lesion. We describe seven children with no physical features of the Marfan syndrome in the patients or their families and no cardiac lesions who had congenital valvular
Publikováno v:
Pediatric Cardiology. 13:181-183
Balloon pulmonary valvuloplasty is a safe and effective treatment for congenital pulmonic valve stenosis. This report describes a child who developed complete atrioventricular (AV) block following balloon pulmonary valvuloplasty. The child was treate
Publikováno v:
Chest. 104(1)
Familial arrhythmogenic right ventricular dysplasia is a rare cardiomyopathy that is usually diagnosed on postmortem examination or on presentation with progressive congestive heart failure. We present a patient in whom an automatic implantable cardi
Autor:
Mary Allen Engle, John E. O'Loughlin, Michael S. Snyder, Kathryn H. Ehlers, Nunzia S. Fatica, Arthur A. Klein, James B. Bussel, Aaron R. Levin
Publikováno v:
Progress in Pediatric Cardiology. 1:96
Autor:
Fukiko Ichida, Nunzia S. Fatica, John E. O'Loughlin, Arthur A. Klein, Michael S. Snyder, Aaron R. Levin, Kathryn H. Ehlers, Martin L. Lesser, Mary Allen Engle
Publikováno v:
Pediatrics. 84:235-241
Epidemiologic and clinical features of Kawasaki disease in 106 patients seen between 1980 and 1986 at The New York Hospital in midtown Manhattan were compared with those in large series from the United States, Canada, and Japan. Dissimilarities in ou
Publikováno v:
Circulation. 55:286-294
His bundle electrograms were recorded in 348 patients aged 2 months to 24 years following routine diagnostic cardiac catheterization. Among 41 children found to be free of anatomic or hemodynamic abnormality the following mean values were obtained: P
Publikováno v:
Chest. 67:685-691
Postangiocardiographic screening of infants and children with congenital heart disease for silent anomalies of the urinary tract yielded an incidence of 7.7 percent in 260 so studied. The incidence was 29 percent in 21 babies who came to autopsy and