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Journal Abstract Search
334 related items for PubMed ID: 25315809
1. A unified approach to risk assessment for fetal aneuploidies. Wright D, Wright A, Nicolaides KH. Ultrasound Obstet Gynecol; 2015 Jan; 45(1):48-54. PubMed ID: 25315809 [Abstract] [Full Text] [Related]
2. Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting. Miltoft CB, Rode L, Ekelund CK, Sundberg K, Kjaergaard S, Zingenberg H, Tabor A. Ultrasound Obstet Gynecol; 2018 Apr; 51(4):470-479. PubMed ID: 28640470 [Abstract] [Full Text] [Related]
3. First-trimester contingent screening for trisomies 21, 18 and 13 by fetal nuchal translucency and ductus venosus flow and maternal blood cell-free DNA testing. Kagan KO, Wright D, Nicolaides KH. Ultrasound Obstet Gynecol; 2015 Jan; 45(1):42-7. PubMed ID: 25307357 [Abstract] [Full Text] [Related]
4. Screening for trisomy 21 by fetal tricuspid regurgitation, nuchal translucency and maternal serum free beta-hCG and PAPP-A at 11 + 0 to 13 + 6 weeks. Falcon O, Auer M, Gerovassili A, Spencer K, Nicolaides KH. Ultrasound Obstet Gynecol; 2006 Feb; 27(2):151-5. PubMed ID: 16388509 [Abstract] [Full Text] [Related]
6. First-trimester contingent screening for trisomy 21 by biomarkers and maternal blood cell-free DNA testing. Nicolaides KH, Wright D, Poon LC, Syngelaki A, Gil MM. Ultrasound Obstet Gynecol; 2013 Jul; 42(1):41-50. PubMed ID: 23744626 [Abstract] [Full Text] [Related]
7. Routine first-trimester screening for fetal trisomies in twin pregnancy: cell-free DNA test contingent on results from combined test. Galeva S, Konstantinidou L, Gil MM, Akolekar R, Nicolaides KH. Ultrasound Obstet Gynecol; 2019 Feb; 53(2):208-213. PubMed ID: 30353581 [Abstract] [Full Text] [Related]
8. First-trimester combined screening for trisomy 21 with different combinations of placental growth factor, free β-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Kagan KO, Hoopmann M, Abele H, Alkier R, Lüthgens K. Ultrasound Obstet Gynecol; 2012 Nov; 40(5):530-5. PubMed ID: 22611005 [Abstract] [Full Text] [Related]
9. Clinical implementation of routine screening for fetal trisomies in the UK NHS: cell-free DNA test contingent on results from first-trimester combined test. Gil MM, Revello R, Poon LC, Akolekar R, Nicolaides KH. Ultrasound Obstet Gynecol; 2016 Jan; 47(1):45-52. PubMed ID: 26498918 [Abstract] [Full Text] [Related]
10. Prospective validation of first-trimester combined screening for trisomy 21. Kagan KO, Etchegaray A, Zhou Y, Wright D, Nicolaides KH. Ultrasound Obstet Gynecol; 2009 Jul; 34(1):14-8. PubMed ID: 19526452 [Abstract] [Full Text] [Related]
11. First-trimester screening for trisomy 21 by free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A: impact of maternal and pregnancy characteristics. Kagan KO, Wright D, Spencer K, Molina FS, Nicolaides KH. Ultrasound Obstet Gynecol; 2008 May; 31(5):493-502. PubMed ID: 18432600 [Abstract] [Full Text] [Related]
12. Fetal nasal bone in screening for trisomies 21, 18 and 13 and Turner syndrome at 11-13 weeks of gestation. Kagan KO, Cicero S, Staboulidou I, Wright D, Nicolaides KH. Ultrasound Obstet Gynecol; 2009 Mar; 33(3):259-64. PubMed ID: 19248005 [Abstract] [Full Text] [Related]
13. UK NHS pilot study on cell-free DNA testing in screening for fetal trisomies: factors affecting uptake. Gil MM, Giunta G, Macalli EA, Poon LC, Nicolaides KH. Ultrasound Obstet Gynecol; 2015 Jan; 45(1):67-73. PubMed ID: 25302655 [Abstract] [Full Text] [Related]
14. Screening for trisomy 18 by maternal age, fetal nuchal translucency, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Kagan KO, Wright D, Maiz N, Pandeva I, Nicolaides KH. Ultrasound Obstet Gynecol; 2008 Sep; 32(4):488-92. PubMed ID: 18726925 [Abstract] [Full Text] [Related]
15. Screening for aneuploidies by maternal age, fetal nuchal translucency and maternal serum biochemistry at 11-13+6 gestational weeks. Karadzov-Orlić N, Egić A, Filimonović D, Marinković M, Damnjanović-Pazin B, Milovanović Z, Joksić I, Branković S, Lukić R, Mandić V, Cerović N, Mojović D, Plamenac S, Stanković M, Maglić D, Mikovć Z. Srp Arh Celok Lek; 2012 Sep; 140(9-10):606-11. PubMed ID: 23289277 [Abstract] [Full Text] [Related]
16. First-trimester contingent screening for trisomies 21, 18 and 13 by biomarkers and maternal blood cell-free DNA testing. Nicolaides KH, Syngelaki A, Poon LC, Gil MM, Wright D. Fetal Diagn Ther; 2014 Sep; 35(3):185-92. PubMed ID: 24192489 [Abstract] [Full Text] [Related]
17. Tricuspid regurgitation in screening for trisomies 21, 18 and 13 and Turner syndrome at 11+0 to 13+6 weeks of gestation. Kagan KO, Valencia C, Livanos P, Wright D, Nicolaides KH. Ultrasound Obstet Gynecol; 2009 Jan; 33(1):18-22. PubMed ID: 19031473 [Abstract] [Full Text] [Related]
18. Two-stage first-trimester screening for trisomy 21 by ultrasound assessment and biochemical testing. Kagan KO, Staboulidou I, Cruz J, Wright D, Nicolaides KH. Ultrasound Obstet Gynecol; 2010 Nov; 36(5):542-7. PubMed ID: 20503223 [Abstract] [Full Text] [Related]
19. Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities. Kagan KO, Sonek J, Wagner P, Hoopmann M. Arch Gynecol Obstet; 2017 Oct; 296(4):645-651. PubMed ID: 28702698 [Abstract] [Full Text] [Related]
20. Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: effect of maternal and fetal factors. Ashoor G, Poon L, Syngelaki A, Mosimann B, Nicolaides KH. Fetal Diagn Ther; 2012 Oct; 31(4):237-43. PubMed ID: 22572044 [Abstract] [Full Text] [Related] Page: [Next] [New Search]