-
Congenital lymphedema presenting with increased nuchal translucency at 13 weeks of gestation.
Souka AP, Krampl E, Geerts L, Nicolaides KH.
Prenat Diagn 2002;22:91-2. -
Hypophosphatasia associated with increased nuchal translucency: a report of two affected pregnancies.
Souka AP, Raymond FL, Mornet E, Geerts L, Nicolaides KH.
Ultrasound Obstet Gynecol 2002;20:294-5. -
Blackfan-Diamond anemia and dyserythropoietic anemia presenting with increased nuchal translucency at 12 weeks of gestation.
Souka AP, Bower S, Geerts L, Huggon I, Nicolaides KH.
Ultrasound Obstet Gynecol 2002;20:197-9. -
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS alpha2gammabetaS) in sickle cell disease.
Ofori-Acquah SF, Green BN, Davies SC, Nicolaides KH, Serjeant GR, Layton DM.
Anal Biochem 2001;298:76-82. -
Prenatal ultrasound diagnosis of Leroy I cell disease.
Lees C, Homfray T, Nicolaides KH.
Ultrasound Obstet Gynecol 2001;18:275-6. -
Screening for trisomy 13 by fetal nuchal translucency and maternal serum free beta hCG and PAPP-A at 10-14 weeks of gestation.
Spencer K, Ong C, Skentou H, Liao AW, Nicolaides KH.
Prenat Diagn 2000;20:411-6. -
Increased fetal nuchal translucency: possible association with esophageal atresia.
Brown RN, Nicolaides KH.
Ultrasound Obstet Gynecol 2000;15:531-2. -
Increased nuchal translucency in trisomy 13 fetuses at 10-14 weeks of gestation.
Snijders RJ, Sebire NJ, Nayar R, Souka A, Nicolaides KH.
Am J Med Genet 1999;86:205-7. -
First-trimester determination of fetal gender by ultrasound.
Efrat Z, Akinfenwa Y, Nicolaides KH.
Ultrasound Obstet Gynecol 1999;13:305-7. -
Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
Seller MJ, Pal K, Moscoso G, Nicolaides K, Hyett JA.
Clin Dysmorphol 1998;7:41-4. -
Audit of prenatal diagnosis for hemoglobin disorders in the United Kingdom The first twenty years.
Modell B, Petrou M, Layton M, Varnavides L, Moisely C, Ward RH, Rodeck C, Nicolaides K, Fitches A, Old J.
Ann N Y Acad Sci 1998;850:420-2. -
Perinatal lung function measurements and prediction of respiratory problems in infancy.
Greenough A, Naik S, Itakura Y, Yuksel B, Cheeseman P, Nicolaides KH.
Physiol Meas 1998;19:421-6. -
Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks gestation.
Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH.
Am J Obstet Gynecol 1997;176:316-9. -
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: The first 20 years.
Modell B, Petrou M, Layton M, Varnavides L, Slater C, Ward R H, Rodeck C, Nicolaides KH, Gibbons S, Fitches A, Old J.
BMJ 1997;315:779-84. -
Prenatal diagnosis of an extensive fetal lymphangioma using ultrasonography, magnetic resonance imaging and cytology.
Kaminopetros P, Jauniaux E, Kane P, Weston M, Nicolaides KH, Campbell DJ.
Br J Radiol 1997;70:750-3. -
Ultrasound screening for congenital uterine anomalies.
Jurkovic D, Gruboeck K, Tailor A, Nicolaides KH.
BJOG 1997;104:1320-1. -
Ultrasound screening for anencephaly at 10-14 of gestation.
Johnson SP, Sebire NJ, Snijders RJM, Tunkel S, Nicolaides KH.
Ultrasound Obstet Gynecol 1997;9:14-6. -
Lethal congenital arthrogryposis presents with increased nuchal translucency at 10-14 weeks of gestation.
Hyett JH, Noble P, Sebire NJ, Snijders RJM, Nicolaides KH.
Ultrasound Obstet Gynecol 1997;9:310-3. -
Evolution of sonographic findings in a fetus with agenesis of the urethra, vagina and rectum.
Carroll SG, Hyett J, Eustace D, Seller MJ, Nicolaides KH.
Prenat Diagn 1996;16:931-3. -
Prenatal diagnosis of triosephosphate isomerase deficiency.
Arya R, Lalloz MR, Nicolaides KH, Bellingham AJ, Layton DM.
Blood 1996;87:4507-9.