Search Results - "Linskens, I."

Why are congenital heart defects being missed? by Nisselrooij, A. E. L., Teunissen, A. K. K., Clur, S. A., Rozendaal, L., Pajkrt, E., Linskens, I. H., Rammeloo, L., Lith, J. M. M., Blom, N. A., Haak, M. C.

“…ABSTRACT Objective Congenital heart defects (CHD) are still missed frequently in prenatal screening programs, which can result in severe morbidity or even…”
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Adverse pregnancy outcome in fetuses with early increased nuchal translucency: prospective cohort study by Bet, B. B., Lugthart, M. A., Linskens, I. H., van Maarle, M. C., van Leeuwen, E., Pajkrt, E.

“…ABSTRACT Objectives An increased nuchal translucency (NT) thickness of ≥ 3.5 mm is a well‐established marker for congenital anomalies and adverse pregnancy…”
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Fetal premature atrial contractions: natural course, risk factors and adverse outcome by Bet, B. B., Eijsbroek, F. C., van Leeuwen, E., Linskens, I. H., Knobbe, I., Clur, S. A., Pajkrt, E.

“…ABSTRACT Objectives Fetal premature atrial contractions (PAC) are usually benign but may be associated with congenital heart defect (CHD) and tachyarrhythmia,…”
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EP06.01: Motor assessment is influenced by experience in systematic motor assessment, elucidated by eye tracking visual approaches: a pilot case‐control study by Tjon, J., Jarodzka, H., Knoop, B., Linskens, I., Vries, J.I.

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EP23.08: Postnatal outcomes of sonographically suspected congenital lung anomalies by Heinrich, H., Kooter, D., Linskens, I., Leeuwen, L., Gorter, R., Oomen, M., Pajkrt, E.

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VP26.10: Metabolic disease with prenatal findings of lissencephaly: progressive porencephaly by Linskens, I., Tjon, J., Elting, M., Pol, L., Vries, J.I.

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Congenital small bowel obstruction: Prenatal detection and outcome by Heinrich, H, Pijpers, A G H, Linskens, I H, van Leeuwen, E, Schattenkerk, L D Eeftinck, Derikx, J P M, Pajkrt, E

“…To evaluate and compare the outcome of fetuses and neonates with congenital small bowel obstructions (SBO), evaluate the screening performance of prenatal…”
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Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies by Lugthart, M. A., Heinrich, H., Ertugrul, I., Nsiah‐Asare, E. N., Kamp, K., Linskens, I. H., Maarle, M. C., Leeuwen, E., Pajkrt, E.

“…Objective To determine whether implementation of cell‐free DNA (cfDNA) testing for aneuploidy as a first‐tier test and subsequent abolition of first trimester…”
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OP05.09: Fetal demise in congenital heart defects: do placenta factors play a role? by Snoep, M., Bet, B., Zwanenburg, F., Knobbe, I., Linskens, I., Clur, S., Rozendaal, L., Van der Meeren, L., Pajkrt, E., Haak, M.C.

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Eye-tracking visual patterns of sonographers with and without fetal motor assessment expertise by Tjon, J.K., Jarodzka, H., Linskens, I.H., Van der Knoop, B.J., De Vries, J.I.P.

“…Fetal motor assessment (FMA) in addition to structural anomaly scan enhances prenatal detection of arthrogryposis multiplex congenita (AMC). In the Amsterdam…”
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EP08.10: Recurrent arachnoid cysts: no known genetic cause? by Tjon, J., Wolf, N., Zwijnenburg, P., Van der Crabben, S., Bakker, P., Linskens, I., Vries, J.I.

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Postnatal outcome of fetal isolated ventricular size disproportion in the absence of aortic coarctation by van Nisselrooij, A. E. L., Rozendaal, L., Linskens, I. H., Clur, S. A., Hruda, J., Pajkrt, E., van Velzen, C. L., Blom, N. A., Haak, M. C.

“…ABSTRACT Objective Cardiac ventricular size disproportion is a marker for aortic coarctation (CoA) in fetal life, but approximately 50% of fetuses do not have…”
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Impact of extracardiac pathology on head growth in fetuses with congenital heart defect by Nisselrooij, A. E. L., Jansen, F. A. R., Geloven, N., Linskens, I. H., Pajkrt, E., Clur, S.‐A., Rammeloo, L. A., Rozendaal, L., Lith, J. M. M., Blom, N. A., Haak, M. C.

“…ABSTRACT Objective Neurodevelopmental delay is frequently encountered in children with a congenital heart defect (CHD). Fetuses with major CHD have a smaller…”
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VP17.13: Timing of prenatal detection of isolated severe congenital heart defects by Lugthart, M.A., Verbaarschot, E., Nisselrooij, A., Kamp, K., Kleinrouweler, E., Haak, M.C., Rozendaal, L., Linskens, I., Hruda, J., Clur, S., Leeuwen, E., Snijders, R., Pajkrt, E.

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OC21.02: The incidence of genetic variants in fetuses with severe congenital heart defects by Nisselrooij, A., Lugthart, M., Santen, G., Aten, E., Clur, S.B., Linskens, I., Pajkrt, E., Rammeloo, L., Van Lith, J., Blom, N., Haak, M.C.

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OC11.01: Why congenital heart defects are being missed by Nisselrooij, A., Teunissen, K., Rozendaal, L., Pajkrt, E., Linskens, I., Hruda, J., Blom, N., Clur, S.B., Haak, M.C.

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OC13.07: The impact of additional anomalies on head growth in fetuses with congenital heart defects by Nisselrooij, A., Jansen, F.A., Geloven, N., Linskens, I., Pajkrt, E., Clur, S.B., Hruda, J., Van Lith, J., Blom, N., Haak, M.C.

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Early first-trimester free β-hCG and PAPP-A serum distributions in monochorionic and dichorionic twins by Linskens, I. H., Spreeuwenberg, M. D., Blankenstein, M. A., van Vugt, J. M. G.

“…Background In the Netherlands, prenatal screening for trisomy 21 in the first trimester of pregnancy for singletons is conducted through a combined test based…”
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A trend toward increased first trimester free β-hCG and PAPP-A in monochorionic twins complicated by Twin-to-Twin Transfusion syndrome by Linskens, I. H., Engels, M., Oepkes, D., Heijboer, A. C., Blankenstein, M. A., van Vugt, J. M. G.

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ADAM12s as a first-trimester screening marker of trisomy by Wortelboer, E. J., Linskens, I. H., Koster, M. P. H., Stoutenbeek, P., Cuckle, H., Blankenstein, M. A., Visser, G. H. A., van Vugt, J. M. G., Schielen, P. C. J. I.

“…Objective To evaluate the potential of maternal serum A Disintegrin And Metalloprotease 12‐S (ADAM12s) as an additional marker for the combined test in the…”
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