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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 5
2004 4
2005 1
2006 1
2009 1
2010 1
2011 1
2012 3
2014 1
2015 1
2016 1
2017 1
2018 1
2019 2
2020 2
2021 1
2022 2
2024 0

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29 results

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Page 1
Disorders of prosencephalic development.
Volpe P, Campobasso G, De Robertis V, Rembouskos G. Volpe P, et al. Among authors: rembouskos g. Prenat Diagn. 2009 Apr;29(4):340-54. doi: 10.1002/pd.2208. Prenat Diagn. 2009. PMID: 19184971 Review.
Perinatal and 2-year neurodevelopmental outcome in late preterm fetal compromise: the TRUFFLE 2 randomised trial protocol.
Mylrea-Foley B, Thornton JG, Mullins E, Marlow N, Hecher K, Ammari C, Arabin B, Berger A, Bergman E, Bhide A, Bilardo C, Binder J, Breeze A, Brodszki J, Calda P, Cannings-John R, Černý A, Cesari E, Cetin I, Dall'Asta A, Diemert A, Ebbing C, Eggebø T, Fantasia I, Ferrazzi E, Frusca T, Ghi T, Goodier J, Greimel P, Gyselaers W, Hassan W, Von Kaisenberg C, Kholin A, Klaritsch P, Krofta L, Lindgren P, Lobmaier S, Marsal K, Maruotti GM, Mecacci F, Myklestad K, Napolitano R, Ostermayer E, Papageorghiou A, Potter C, Prefumo F, Raio L, Richter J, Sande RK, Schlembach D, Schleußner E, Stampalija T, Thilaganathan B, Townson J, Valensise H, Visser GH, Wee L, Wolf H, Lees CC; TRUFFLE 2 Collaborators List. Mylrea-Foley B, et al. BMJ Open. 2022 Apr 15;12(4):e055543. doi: 10.1136/bmjopen-2021-055543. BMJ Open. 2022. PMID: 35428631 Free PMC article.
Sonographic markers of fetal aneuploidy--a review.
Cicero S, Sacchini C, Rembouskos G, Nicolaides KH. Cicero S, et al. Among authors: rembouskos g. Placenta. 2003 Oct;24 Suppl B:S88-98. doi: 10.1016/s0143-4004(03)00141-3. Placenta. 2003. PMID: 14559037 Review.
Nasal bone in first-trimester screening for trisomy 21.
Cicero S, Avgidou K, Rembouskos G, Kagan KO, Nicolaides KH. Cicero S, et al. Among authors: rembouskos g. Am J Obstet Gynecol. 2006 Jul;195(1):109-14. doi: 10.1016/j.ajog.2005.12.057. Am J Obstet Gynecol. 2006. PMID: 16813749
Incidence of chromosomal abnormalities in fetuses with first trimester ultrasound anomalies and a low-risk cell-free DNA test for common trisomies.
Persico N, Boito S, Volpe P, Ischia B, Gentile M, Ronzoni L, De Robertis V, Fabietti I, Olivieri C, Periti E, Ficarella R, Silipigni R, Rembouskos G. Persico N, et al. Among authors: rembouskos g. Prenat Diagn. 2020 Oct;40(11):1474-1481. doi: 10.1002/pd.5799. Epub 2020 Aug 9. Prenat Diagn. 2020. PMID: 33034897 Free article.
29 results