Zobrazeno 1 - 10 of 23 pro vyhledávání: '"M E, Norton"'
1
Outcomes of pregnancies with more than one positive prenatal screening result in the first or second trimester
Autor: R J, Baer, R J, Currier, M E, Norton, M C, Flessel, S, Goldman, D, Towner, L L, Jelliffe-Pawlowski
Publikováno v: Prenatal diagnosis. 35(12)
To describe adverse outcomes and fetal abnormalities in women with a positive prenatal screening result for more than one disorder.Study participants were drawn from a population of 452 901 women pregnant with singletons entering the California Prena
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b225669c90f8cc5e8789f63a2439b2b
https://pubmed.ncbi.nlm.nih.gov/26288069
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3
Ethnic variation in the prevalence of echogenic intracardiac foci and the association with Down syndrome
Autor: S H, Tran, A B, Caughey, M E, Norton
Publikováno v: Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 26(2)
To determine whether the prevalence of fetal echogenic intracardiac foci (EIF) differs according to maternal ethnicity.We performed a retrospective cohort study of all women undergoing second-trimester diagnostic ultrasound examination and amniocente
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32facde2688c5e3c66739d73cce51e05
https://pubmed.ncbi.nlm.nih.gov/16038014
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4
Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p
Autor: E M, McGhee, Y, Qu, M M, Wohlferd, J D, Goldberg, M E, Norton, P D, Cotter
Publikováno v: Clinical genetics. 59(4)
Monosomy for the short arm of chromosome 18 is one of the most frequent autosomal deletions observed. While most cases result from terminal deletion of 18p, 16% of cases reported were as a result of an unbalanced whole arm translocation resulting in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6a2a50b4bc167f88ac894202f7c26fba
https://pubmed.ncbi.nlm.nih.gov/11298684
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6
Behçet's syndrome associated with intrauterine growth restriction: a case report and review of the literature
Autor: G, Guzelian, M E, Norton
Publikováno v: Journal of perinatology : official journal of the California Perinatal Association. 17(4)
Behçet's syndrome is an immune-mediated connective tissue disorder, and its primary manifestations are oral and genital ulcerations. To our knowledge no cases of adverse fetal outcome have been reported in pregnancies complicated by this disease.A 2
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f3d32b8414bca17880e9f47e07b4eecd
https://pubmed.ncbi.nlm.nih.gov/9280100
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7
Biochemical and ultrasound screening for chromosomal abnormalities
Autor: M E, Norton
Publikováno v: Seminars in perinatology. 18(4)
The utility of ultrasound screening for Down syndrome should be judged by whether the pertinent markers are reliably obtained and by whether they efficiently discriminate between fetuses with Down syndrome and euploid fetuses. Furthermore, the marker
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d763e80ce867d124ac775106ef9919bf
https://pubmed.ncbi.nlm.nih.gov/7527158
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8
Nonimmune hydrops fetalis
Autor: M E, Norton
Publikováno v: Seminars in perinatology. 18(4)
In summary, NIHF is a heterogenous disorder resulting from a vast number of underlying pathologies. A thorough evaluation should be performed in all cases to attempt to establish the etiology. This requires a systematic approach that should logically
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9a9d14f25cc73e4a3b4e37afb873ef04
https://pubmed.ncbi.nlm.nih.gov/7985044
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