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Value of routine ultrasound examination at 35-37 weeks' gestation in diagnosis of fetal abnormalities.
Ficara A, Syngelaki A, Hammami A, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol 2020;55:75-80. pdf -
Diagnosis of fetal defects in twin pregnancies at routine 11-13-week ultrasound examination.
Syngelaki A, Cimpoca B, Litwinska E, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol 2020;55:474-481. pdf -
Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation.
Syngelaki A, Hammami A, Bower S, Zidere V, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol 2019;54:468-476. pdf -
Maternal autoimmune disorders and fetal defects.
Panaitescu AM, Nicolaides K.
J Matern Fetal Neonatal Med 2018;31:1798-1806. pdf -
Impact of holoprosencephaly, exomphalos, megacystis and increased nuchal translucency on first-trimester screening for chromosomal abnormalities.
Syngelaki A, Guerra L, Ceccacci I, Efeturk T, Nicolaides KH.
Ultrasound Obstet Gynecol 2017;50:45-48. pdf -
Embryo-fetal erythroid cell selection from celomic fluid allows earlier prenatal diagnosis of hemoglobinopathies.
Giambona A, Damiani G, Leto F, Jakil C, Renda D, Cigna V, Schillaci G, Picciotto F, Nicolaides KH, Passarello C, Makrydimas G, Maggio A.
Prenat Diagn 2016;36:375-81. pdf -
Maternal and pregnancy characteristics affect plasma fibrin monomer complexes and D-dimer reference ranges for venous thromboembolism in pregnancy.
Grossman KB, Arya R, Peixoto AB, Akolekar R, Staboulidou I, Nicolaides KH.
Am J Obstet Gynecol 2016;215:466.e1-8. pdf -
A case-control study of maternal periconceptual and pregnancy recreational drug use and fetal malformation using hair analysis.
David AL, Holloway A, Thomasson L, Syngelaki A, Nicolaides K, Patel RR, Sommerlad B, Wilson A, Martin W, Chitty LS.
PLoS One 2014;9:e111038. pdf -
Clinical significance of first-trimester chorionic bumps: a matched case-control study.
Sana Y, Appiah A, Davison A, Nicolaides KH, Johns J, Ross JA.
Ultrasound Obstet Gynecol 2013;42:585-9. -
Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks.
Syngelaki A, Chelemen T, Dagklis T, Allan L, Nicolaides KH.
Prenat Diagn 2011;31:90-102. -
A model for a new pyramid of prenatal care based on the 11 to 13 weeks' assessment.
Nicolaides KH.
Prenat Diagn 2011;31:3-6. -
Turning the pyramid of prenatal care.
Nicolaides KH.
Fetal Diagn Ther 2011;29:183-96. -
Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis.
Giambona A, Makrydimas G, Leto F, Damiani G, Jakil MC, Picciotto F, Renda D, Fiorino R, Renda MC, Schillaci G, Gueli-Alletti D, Nicolaides KH, Maggio A.
Br J Haematol 2011;153:268-72. -
The 11-13-week scan: diagnosis and outcome of holoprosencephaly, exomphalos and megacystis.
Kagan KO, Staboulidou I, Syngelaki A, Cruz JJ, Nicolaides KH.
Ultrasound Obstet Gynecol 2010;36:10-4. -
Isolated single umbilical artery: need for specialist fetal echocardiography.
Defigueiredo D, Dagklis T, Zidere V, Allan L, Nicolaides KH.
Ultrasound Obstet Gynecol 2010;36:553-5. -
Choroid plexus cyst, intracardiac echogenic focus, hyperechogenic bowel and hydronephrosis in screening for trisomy 21 at 11 + 0 to 13 + 6 weeks.
Dagklis T, Plasencia W, Maiz N, Duarte L, Nicolaides KH.
Ultrasound Obstet Gynecol 2008;31:132-5. -
Some thoughts on the true value of ultrasound.
Nicolaides KH.
Ultrasound Obstet Gynecol 2007;30:671-4. -
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variation.
Gerovassili A, Nicolaides KH, Thein SL, Rees DC.
Br J Haematol 2006;135:738-41. -
Increased nuchal translucency with normal karyotype.
Souka AP, Von Kaisenberg CS, Hyett JA, Sonek JD, Nicolaides KH.
Am J Obstet Gynecol 2005;192:1005-21. -
Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester.
Souka AP, Krampl E, Bakalis S, Heath V, Nicolaides KH.
Ultrasound Obstet Gynecol 2001;18:9-17.