Zobrazeno 1 - 10
of 15
pro vyhledávání: '"O B, Petersen"'
Autor:
C. Vedel, T. D. Hjortshøj, D. S. Jørgensen, A. Tabor, L. Rode, K. Sundberg, C. K. Ekelund, O. B. Petersen
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 61:40-48
To estimate the prevalence of chromosomal conditions in all fetuses and children with major congenital heart defect (CHD) in Denmark between 2008 and 2018.This was a national registry-based study including all singleton pregnancies with a prenatally
Autor:
S. E. Kristensen, K. Gadsbøll, K. H. Nicolaides, I. Vogel, L. H. Pedersen, A. Wright, O. B. Petersen, D. Wright
Publikováno v:
Kristensen, S E, Gadsbøll, K, Nicolaides, K H, Vogel, I, Pedersen, L H, Wright, A, Petersen, O B & Wright, D 2023, ' Atypicality index : avoiding false reassurance in prenatal screening ', Ultrasound in Obstetrics & Gynecology, vol. 61, no. 3, pp. 333-338 . https://doi.org/10.1002/uog.26135
OBJECTIVE: To demonstrate the application of an individual atypicality index as an adjunct to first trimester risk assessment for major trisomies by the combined test.METHODS: Atypicality indices were produced for measurements of fetal nuchal translu
Publikováno v:
Kristiansen, M K, Joensen, BS, Ekelund, CK, Petersen, O B, Sandager, P & with the Danish Fetal Medicine Study Group 2015, ' Perinatal outcome after first-trimester risk assessment in monochorionic and dichorionic twin pregnancies : a population-based register study ', B J O G, vol. 122, no. 10, pp. 1362-69 . https://doi.org/10.1111/1471-0528.13326
Objective To evaluate the influence of chorionicity on outcome in twin pregnancies with two live fetuses at the nuchal translucency scan in the first trimester. Design Population-based register study. Setting Denmark. Population A cohort of 3621 twin
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 51(4)
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 51(4)
To evaluate the performance of high-resolution chromosomal microarray (CMA) as the standard diagnostic approach for genomic imbalances in pregnancies with increased risk based on combined first-trimester screening (cFTS).This was a retrospective stud
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 51(5)
To assess cervical length (CL) longitudinally between the first and second trimesters and to determine the proportion of women with short CL. The study also aimed to assess if women with short CL at 19-24 weeks' gestation could be identified at the t
Autor:
D. Wright, K. Spencer, K. Kagan K, N. Tørring, O. B. Petersen, A. Christou, J. Kallikas, K. H. Nicolaides
Publikováno v:
Wright, D, Spencer, K, Kagan K, K, Tørring, N, Petersen, O B, Christou, A, Kallikas, J & Nicolaides, K H 2010, ' First-trimester combined screening for trisomy 21 at 7-14 weeks' gestation ', Ultrasound in Obstetrics & Gynecology, vol. 36, no. 4, pp. 404-11 . https://doi.org/10.1002/uog.7755
Objective To establish an algorithm for first-trimester combined screening for trisomy 21 with biochemical testing from 7 to 14 weeks’ gestation and ultrasound testing at 11–13 weeks. Methods This was a multicenter study of 886 pregnancies with t
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 47(1)
To assess prospectively the risk of fetal loss associated with chorionic villus sampling (CVS) and amniocentesis (AC) following combined first-trimester screening (cFTS) for Down syndrome.This was a nationwide population-based study (Danish Fetal Med
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 43(3)
Targeted non-invasive prenatal testing (NIPT) tests for trisomies 21, 18 and 13 and sex chromosome aneuploidies and could be an alternative to traditional karyotyping. The aim of this study was to determine the risk of missing other abnormal karyotyp
Autor:
C, Ekelund, D, Wright, S, Ball, I, Kirkegaard, P, Nørgaard, S, Sørensen, L, Friis-Hansen, F S, Jørgensen, N, Tørring, B H, Bech, O B, Petersen, A, Tabor
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 40(3)
To prospectively evaluate the performance of first-trimester combined screening for trisomy 21 using the biochemical markers pregnancy-associated plasma protein-A (PAPP-A) and free beta-human chorionic gonadotropin (free β-hCG) obtained before and a