Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Charlotte Ferencz"'
Autor:
Charlotte Ferencz
Publikováno v:
Circulation. 33(2)
A microscopic study of the lungs of 106 patients with transposition of the great vessels has revealed early and severe hypertensive alterations in the pulmonary arteries. These striking changes, associated in almost all instances with normal pulmonar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e599f40510e1f1123dc8129dd3da0cd1
https://pubmed.ncbi.nlm.nih.gov/25823090
https://pubmed.ncbi.nlm.nih.gov/25823090
Autor:
Christopher A. Loffredo, Muin J. Khoury, Lorenzo D. Botto, Charlotte Ferencz, P. David Wilson, Kelley S. Scanlon, Adolfo Correa
Publikováno v:
Epidemiology. 12:491-496
To assess the relationship between maternal intake of vitamin A and cardiac outflow tract defects, we examined data from a population-based case-control study among liveborn infants born from 1987 through 1989 to mothers residing in the Baltimore-Was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8817a29636d29f7d2f059fcd75e7e049
https://doi.org/10.1097/00001648-200109000-00005
https://doi.org/10.1097/00001648-200109000-00005
Publikováno v:
Teratology. 64:98-106
Background Intensive medical care of women with diabetes has reduced their risks of bearing infants with congenital anomalies. To assess the preventive potential of preconceptional care, the data of a population-based study of cardiovascular malforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a518e9f8bfbe99749f1389a2fb915eb
https://doi.org/10.1002/tera.1051
https://doi.org/10.1002/tera.1051
Atrioventricular septal defects: Possible etiologic differences between complete and partial defects
Publikováno v:
Teratology. 63:87-93
Background Recent advances in clinical, pathological, and genetic aspects of atrioventricular septal defects (AVSD) have set the stage for epidemiologic investigations into possible risk factors. Previous analyses of the total case group of AVSD incl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::207438ed870f38e0ac8dbe13bddd7c6d
https://doi.org/10.1002/1096-9926(200102)63:2<87::aid-tera1014>3.0.co
https://doi.org/10.1002/1096-9926(200102)63:2<87::aid-tera1014>3.0.co
Publikováno v:
Teratology. 64:229-236
Background Coarctation of the aorta (CoA) is a congenital cardiovascular malformation (CCVM) sometimes associated with ventricular septal defect (VSD). Although the phenotypic association is well documented, little research exists on the epidemiologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1733c1bb8e975b4d0bd046d757a3c6f
https://doi.org/10.1002/tera.1069
https://doi.org/10.1002/tera.1069
Publikováno v:
Teratology. 61:368-375
Background: Interruption of the aortic arch (IAA) is a rare but severe anomaly associated with major intracardiac defects and with multisystem noncardiac malformations, recently linked to chromosome deletion of 22q11.2. Methods: The Baltimore-Washing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88314c20f5e1ef44ba68dbce92f6f82b
https://doi.org/10.1002/(sici)1096-9926(200005)61:5<368::aid-tera8>3.0.co
https://doi.org/10.1002/(sici)1096-9926(200005)61:5<368::aid-tera8>3.0.co
Publikováno v:
American Journal of Epidemiology. 148:414-423
To the authors' knowledge, attributable fractions for cardiac malformations have not been reported before. The Baltimore-Washington Infant Study published factors associated with several major cardiac malformations in Maryland, the District of Columb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a791d3e21956ce1ec2846657f881cde
https://doi.org/10.1093/oxfordjournals.aje.a009666
https://doi.org/10.1093/oxfordjournals.aje.a009666
Autor:
Adolfo Correa-Villaseñor, Charlotte Ferencz, P D Wilson, Kelley S. Scanlon, Walter C. Willett, Christopher A. Loffredo, Muin J. Khoury
Publikováno v:
Epidemiology. 9:95-98
We compared cases with outflow tract defects (N = 126) with controls representative of the same birth cohort (N = 679). Infants with clinically recognized syndromes were excluded. Daily total maternal folate intake of > or =245 microg was inversely r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7d03239af729fac4d73fb0167d23e9f
https://doi.org/10.1097/00001648-199801000-00019
https://doi.org/10.1097/00001648-199801000-00019
Autor:
Charlotte Ferencz, Iosif W. Lurie
Publikováno v:
American Journal of Medical Genetics. 70:144-149
Phenotypic manifestations of the autosomal recessive form of VACTERL-hydrocephaly syndrome (David-O'Callaghan syndrome) and the X-linked recessive form (Hunter-MacMurray) syndrome are almost identical. The absence of cardiovascular malformations in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b146d7834111644bdcf145e9d9784eb3
https://doi.org/10.1002/(sici)1096-8628(19970516)70:2<144::aid-ajmg8>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19970516)70:2<144::aid-ajmg8>3.0.co
Publikováno v:
Progress in Pediatric Cardiology. 5:73-78
Advances in ultrasound technology and its widespread application have enabled the discovery of the most serious cardiovascular malformations in 16–18 week fetuses. The type of CVM is a major, but not the only, factor determining parental decision r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9ee607ff0ea0c43776c97ce399337c
https://doi.org/10.1016/1058-9813(95)00152-2
https://doi.org/10.1016/1058-9813(95)00152-2