Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Paul Stanger"'
Publikováno v:
Cardiology in the Young. 9:300-304
BackgroundTricuspid regurgitation as a manifestation of an isolated congenital anomaly of the tricuspid valve is rare. Cross-sectional and color Doppler echocardiography allow improved evaluation of tricuspid valvar function. As a result, the heterog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f9ca94e7ade860832aa9b66e2faa8a
https://doi.org/10.1017/s1047951100004972
https://doi.org/10.1017/s1047951100004972
Publikováno v:
The Annals of Thoracic Surgery. 65:1120-1126
Background . Stenosis of the branch pulmonary arteries after tetralogy of Fallot repair can result from several mechanisms. In patients with free pulmonary regurgitation and right ventricular dilatation after transannular patch repair, we have observ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d57a16195c66284028ec71e6b6fc0eb
https://doi.org/10.1016/s0003-4975(98)00112-x
https://doi.org/10.1016/s0003-4975(98)00112-x
Publikováno v:
Journal of the American College of Cardiology. 19:1285-1293
To determine the current risk of pediatric cardiac catheterization, the complications and incidents of all catheterizations performed in a pediatric laboratory between January 1986 and October 1988 were prospectively recorded and compared with result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ef848bb589e9a415d7cfac458fb442
https://doi.org/10.1016/0735-1097(92)90336-l
https://doi.org/10.1016/0735-1097(92)90336-l
Publikováno v:
Cardiology in the Young. 10:618-620
Deletions of chromosome 22q11 are common in patients with tetralogy of Fallot, and in those with absent pulmonary valve syndrome. In this report, we describe a pair of siblings with absent pulmonary valve syndrome, neither of whom had deletions of ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d5a86e8b188491983de83b4b48c0e2
https://doi.org/10.1017/s1047951100008908
https://doi.org/10.1017/s1047951100008908
Autor:
Donald A. Girod, Paul Stanger, Stephen R. Shapiro, Zuhdi Lababidi, Steven C. Cassidy, Jean S. Kan
Publikováno v:
The American Journal of Cardiology. 65:784-789
Data from 204 children and infants who underwent aortic balloon valvuloplasty between 1982 and 1986, reported to the Valvuloplasty and Angioplasty of Congenital Anomalies Registry, were reviewed. Valvuloplasty was successful in 192 of 204 children, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52caa810f1cd386b8e38acc3aad5abe2
https://doi.org/10.1016/0002-9149(90)91388-m
https://doi.org/10.1016/0002-9149(90)91388-m
Publikováno v:
The American journal of cardiology. 83(6)
Although cardiologists who treat adults have been evaluating pediatric patients using echocardiography since the early 1980s, the diagnostic accuracy of such studies has never been tested. To prospectively assess diagnostic accuracy of pediatric echo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16fd1e421680bcbc846ff617e33bd63b
https://pubmed.ncbi.nlm.nih.gov/10190408
https://pubmed.ncbi.nlm.nih.gov/10190408
Autor:
V. Mohan Reddy, Michael M. Brook, Doff B. McElhinney, Frank L. Hanley, Norman H. Silverman, Paul Stanger
Publikováno v:
The Annals of thoracic surgery. 66(1)
Background . Congenital abnormalities of the tricuspid valve, including Ebstein's malformation, dysplasia, straddling, and those found in pulmonary atresia with intact septum and congenitally corrected transposition, are an uncommon cause of tricuspi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ab2fcc510fa8dfd31e87c6510becb7
https://pubmed.ncbi.nlm.nih.gov/9692459
https://pubmed.ncbi.nlm.nih.gov/9692459
Autor:
V. Mohan Reddy, Doff B. McElhinney, Michael M. Brook, John R. Liddicoat, Paul Stanger, Frank L. Hanley
Publikováno v:
The Annals of thoracic surgery. 60
Background Although primary repair of tetralogy of Fallot is increasingly undertaken in infancy, complete repair is generally performed in only selected symptomatic neonates. Methods From July 1992 through March 1995, 30 consecutive neonates and youn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b5a837cc9d6c73f7d7fa85bb8b9ea2
https://pubmed.ncbi.nlm.nih.gov/8604943
https://pubmed.ncbi.nlm.nih.gov/8604943
Autor:
George F. Van Hare, Paul Stanger
Publikováno v:
The American journal of cardiology. 67(1)
Fourteen infants aged less than 1 month presented to our institution during the last 22 years with ventricular tachycardia (VT) or accelerated ventricular rhythm and a structurally normal heart. In 2, VT was associated with long QT syndrome. Both are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d5771de7a0334acfab03c90aef6e919
https://pubmed.ncbi.nlm.nih.gov/1892117
https://pubmed.ncbi.nlm.nih.gov/1892117
Autor:
Sarah S. Higgins, Renee Dery, Lisa Diethelm, Paul Stanger, Charles B. Higgins, Barbara A Kersting-Sommerhoff, Stanley M Higashino
Publikováno v:
American heart journal. 120(1)
Complex ventricular anomalies are frequently associated with abnormalities of thoracic and abdominal situs, arterioventricular connection, and venous connection. The definition of all components of these anomalies is difficult to accomplish with imag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5502dd37ff557ff9f4d4599b8965d7
https://pubmed.ncbi.nlm.nih.gov/2360498
https://pubmed.ncbi.nlm.nih.gov/2360498