Nicholas J. Cowans
Harold Wood Hospital
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Publication
Featured researches published by Nicholas J. Cowans.
Ultrasound in Obstetrics & Gynecology | 2007
Kevin Spencer; Nicholas J. Cowans; Ilana Chefetz; J. Tal; Hamutal Meiri
To evaluate whether measurement of maternal serum placental protein‐13 (PP‐13) and pregnancy‐associated plasma protein‐A (PAPP‐A) at 11 + 0 to 13 + 6 weeks of gestation alone or in combination with second‐trimester uterine artery pulsitility measured by Doppler velocimetry is useful in predicting those women who will develop pre‐eclampsia
Ultrasound in Obstetrics & Gynecology | 2008
Kevin Spencer; Nicholas J. Cowans; K. Avgidou; F. Molina; Kypros H. Nicolaides
To examine the clinical utility of the first‐trimester biochemical markers of aneuploidy in their ability to predict subsequent delivery of a small‐for‐gestational age (SGA) infant.
Ultrasound in Obstetrics & Gynecology | 2008
Kevin Spencer; Nicholas J. Cowans; F. Molina; Karl Oliver Kagan; Kypros H. Nicolaides
To examine the clinical utility of the first‐trimester markers of aneuploidy in their ability to predict preterm delivery.
Ultrasound in Obstetrics & Gynecology | 2010
Asma Khalil; Nicholas J. Cowans; Kevin Spencer; Sergey Goichman; Hamutal Meiri; Kevin Harrington
To investigate the predictive value of the combination of first‐trimester serum placental protein 13 (PP13), uterine artery Doppler pulsatility index (PI) and pulse wave analysis (augmentation index at a heart rate of 75 beats per min (AIx‐75)), and to evaluate concurrent and contingent strategies using this combination for assessing the risk of pre‐eclampsia in high‐risk women.
Ultrasound in Obstetrics & Gynecology | 2006
Kevin Spencer; Nicholas J. Cowans; K. Avgidou; Kypros H. Nicolaides
To examine the clinical utility of the first‐trimester markers of aneuploidy in their ability to predict future fetal loss.
Prenatal Diagnosis | 2008
Kevin Spencer; Nicholas J. Cowans; Anastasia Stamatopoulou
To examine whether maternal serum ADAM12s, a potential first‐ and second‐trimester marker of fetal aneuploidy and fetal growth, had altered concentrations in the first or second trimester of pregnancies subsequently developing pre‐eclampsia.
Prenatal Diagnosis | 2006
Jennie Laigaard; Kevin Spencer; Michael Christiansen; Nicholas J. Cowans; Severin Olesen Larsen; Bent Nørgaard Pedersen; Ulla M. Wewer
A Disintegrin And Metalloprotease 12 (ADAM 12) is a glycoprotein synthesised by placenta and it has been shown to be a potential first‐trimester maternal serum marker for Down syndrome (DS) in two small series. Here we analyse further, the potential of ADAM 12 as a marker for DS in a large collection of first‐trimester serum samples.
Prenatal Diagnosis | 2009
Asma Khalil; Nicholas J. Cowans; Kevin Spencer; Sergey Goichman; Hamutal Meiri; Kevin Harrington
To evaluate whether first trimester maternal serum PP13 can predict pre‐eclampsia among women with a priori high risk.
Ultrasound in Obstetrics & Gynecology | 2008
Kevin Spencer; Nicholas J. Cowans; Kypros H. Nicolaides
To evaluate whether measurement of maternal serum inhibin‐A and activin‐A at 11 + 0 to 13 + 6 weeks of gestation, alone or in combination with second‐trimester uterine artery pulsatility measured by Doppler velocimetry, is useful in predicting those women who will develop pre‐eclampsia.
Prenatal Diagnosis | 2008
Nicholas J. Cowans; Kevin Spencer; Hamutal Meiri
In a previous study, reduced levels of maternal serum placental protein 13 (PP13) in the first trimester have been correlated with adverse pregnancy outcomes. The objective of this study was to compare first‐trimester PP13 levels in control pregnancies with pregnancies resulting in one or more of the following adverse outcomes: intrauterine growth restriction (IUGR), small and very small (3rd, 5th, 10th centile) for gestational age (SGA), low (<1.5 and < 2.5 kg) birth weight (LBW), macrosomia (the > 90th centile), large birth weight (>4.5 kg), preterm (35–36 weeks) and very early (<34 weeks) delivery (PTD), and intrauterine fetal demise (IUFD).