http://orcid.org/0000-0001-8254-7525
References
- Statistical report 6/2014; 28.2.2014. Official statistics of Finland, Congenital malformations. National Institute for Health and Welfare. http://urn.fi/URN:NBN:fi-fe201706207383
- Ott WJ. The accuracy of antenatal fetal echocardiography screening in high- and low-risk patients. Am J Obstet Gynecol. 1995;172(6):1741–1747.
- Buskens E, Grobbee DE, Frohn-Mulder IM, et al. Efficacy of routine fetal ultrasound screening for congenital heart disease in normal pregnancy. Circulation. 1996;94(1):67–72.
- Carvalho JS, Mavrides E, Shinebourne EA, et al. Improving the effectiveness of routine prenatal screening for major congenital heart defects. Heart. 2002;88(4):387–391.
- Srivastava D. Making or breaking the heart: from lineage determination to morphogenesis. Cell. 2006; 126(6):1037–1048.
- Ghi T, Huggon IC, Zosmer N, et al. Incidence of major structural cardiac defects associated with increased nuchal translucency but normal karyotype. Ultrasound Obstet Gynecol. 2001;18(6):610–614.
- Alanen J, Leskinen M, Sairanen M, et al. Fetal nuchal translucency in severe congenital heart defects: experiences in Northern Finland. J Matern Fetal Neonatal Med. 2017;3:1–7.
- Ruiz A, Ferrer Q, Sánchez O, et al. Placenta-related complications in women carrying a foetus with congenital heart disease. J Matern Fetal Neonatal Med. 2016;29(20):3271–3275.
- Fantasia I, Kasapoglu D, Kasapoglu T, et al. Fetal major cardiac defects and placental dysfunction at 11–13 weeks. Ultrasound Obstet Gynecol. 2017;51(2):194–198.
- Llurba E, Sánchez O, Ferrer Q, et al. Maternal and foetal angiogenic imbalance in congenital heart defects. Eur Heart J. 2014;35(11):701–707.
- Merilainen A, Peuhkurinen S, Honkasalo T, et al. Combined first-trimester screening in northern Finland: experiences of the first ten years. Clin Med Insights Reprod Health. 2014;8(8):45–49.
- Borelli M, Baer RJ, Chambers CD, et al. Critical congenital heart defects and abnormal levels of routinely collected first- and second-trimester biomarkers. Am J Med Genet A. 2017;173(2):368–374.