Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Caterina M Bilardo"'
Autor:
Francesca Bardi, Merel Bakker, Ayten Elvan-Taşpınar, Monique J A Kenkhuis, Jeske Fridrichs, Marian K Bakker, Erwin Birnie, Caterina M Bilardo
Publikováno v:
PLoS ONE, Vol 18, Iss 2, p e0279770 (2023)
IntroductionFirst-trimester anatomical screening (FTAS) by ultrasound has been introduced in many countries as screening for aneuploidies, but also as early screening for fetal structural abnormalities. While a lot of emphasis has been put on the det
Externí odkaz:
https://doaj.org/article/6b68aee404684deaa0c8b2c566494163
Autor:
Francesca Bardi, Merel Bakker, Monique J A Kenkhuis, Adelita V Ranchor, Marian K Bakker, Ayten Elvan, Erwin Birnie, Caterina M Bilardo
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245938 (2021)
IntroductionThe primary aim of this study is to investigate the impact of a 13-week anomaly scan on the experienced levels of maternal anxiety and well-being. Secondly, to explore women's knowledge on the possibilities and limitations of the scan and
Externí odkaz:
https://doaj.org/article/179a72f79e10424aa9bf4048f93bdbb9
Autor:
Iris Bekkering, Mariëtte Leeuwerke, Jozien C Tanis, Mirthe H Schoots, Rikst Nynke Verkaik-Schakel, Torsten Plösch, Caterina M Bilardo, Jasper J H Eijsink, Arend F Bos, Sicco A Scherjon
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0221972 (2019)
BackgroundIn Fetal Growth Restriction 'fetal programming' may take place via DNA methylation, which has implications for short-term and long-term health outcomes. Small-for-gestational age fetuses are considered fetal growth restricted, characterized
Externí odkaz:
https://doaj.org/article/ab3b86b537444d429f40d93c55b19793
Autor:
Anne S. Siegmund, Tineke P. Willems, Petronella G. Pieper, Caterina M. Bilardo, Thomas M. Gorter, Berto J. Bouma, Monique R. M. Jongbloed, Gertjan Tj. Sieswerda, Jolien W. Roos-Hesselink, Arie P. J. van Dijk, Dirk J. van Veldhuisen, Michael G. Dickinson
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 22, Iss 1, Pp 1-8 (2020)
Abstract Background Maternal right ventricular (RV) dysfunction (measured by echocardiography) is associated with impaired uteroplacental circulation, however echocardiography has important limitations in the assessment of RV function. We therefore a
Externí odkaz:
https://doaj.org/article/8b921f6954b04bcfa42b2cc4289ae345
Autor:
Anne E. Richter, Sahar Salavati, Elisabeth M. W. Kooi, Anne E. den Heijer, Anne B. Foreman, Mirthe H. Schoots, Caterina M. Bilardo, Sicco A. Scherjon, Jozien C. Tanis, Arend F. Bos
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Objectives: To assess the role of fetal brain-sparing and postnatal cerebral oxygen saturation (rcSO2) as determinants of long-term neurodevelopmental outcome following fetal growth restriction (FGR).Methods: This was a prospective follow-up study of
Externí odkaz:
https://doaj.org/article/e87218f405904a2a9c48a4d0564fa19d
Autor:
Anne E Richter, Arend F. Bos, Torsten Plösch, Rikst Nynke Verkaik-Schakel, Elisabeth M. W. Kooi, Iris Bekkering-Bauer, Mariëtte Leeuwerke, Sicco A. Scherjon, Jozien C. Tanis, Caterina M. Bilardo
Publikováno v:
Richter, A E, Bekkering-Bauer, I, Verkaik-Schakel, R N, Leeuwerke, M, Tanis, J C, Bilardo, C M, Kooi, E M W, Scherjon, S A, Bos, A F & Plösch, T 2021, ' Altered neurodevelopmental DNA methylation status after fetal growth restriction with brain-sparing ', Journal of Developmental Origins of Health and Disease . https://doi.org/10.1017/S2040174421000374
Journal of developmental origins of health and disease, 13(3), 378-389. Cambridge University Press
Journal of Developmental Origins of Health and Disease. Cambridge University Press
Journal of developmental origins of health and disease, 13(3), 378-389. Cambridge University Press
Journal of Developmental Origins of Health and Disease. Cambridge University Press
It is under debate how preferential perfusion of the brain (brain-sparing) in fetal growth restriction (FGR) relates to long-term neurodevelopmental outcome. Epigenetic modification of neurotrophic genes by altered fetal oxygenation may be involved.
Autor:
Anne S. Siegmund, Petronella G. Pieper, Caterina M. Bilardo, Sanne J. Gordijn, T. Yee Khong, Wilfried Gyselaers, Dirk J. van Veldhuisen, Michael G. Dickinson
Publikováno v:
Siegmund, A S, Pieper, P G, Bilardo, C M, Gordijn, S J, Khong, T Y, Gyselaers, W, van Veldhuisen, D J & Dickinson, M G 2022, ' Cardiovascular determinants of impaired placental function in women with cardiac dysfunction ', American Heart Journal, vol. 245, pp. 126-135 . https://doi.org/10.1016/j.ahj.2021.11.020
Female heart disease has for a long time been an underrecognized problem in the field of cardiology. With an ever-growing number of these patients getting pregnant, cardiac dysfunction during pregnancy is an increasingly large medical problem. Previo
Autor:
Syanni A, Kristalijn, Karen, White, Deanna, Eerbeek, Emilia, Kostenko, Francesca Romana, Grati, Caterina M, Bilardo
Publikováno v:
BMC Pregnancy and Childbirth. 22
Background Non-invasive prenatal testing (NIPT) as a screening method for trisomy 21 and other chromosomal abnormalities has been adopted widely across the globe. However, while many clinical validation studies have been performed, less is known rega
Autor:
Francesca Bardi, Bo B. Bet, Eva Pajkrt, Ingeborg H. Linskens, Mireille N. Bekker, Erik A. Sistermans, Caterina M. Bilardo, Ayten Elvan‐Taşpınar
Publikováno v:
Prenatal Diagnosis, 42(1). Wiley-Blackwell
Prenatal diagnosis, 42(11), 1358-1367. John Wiley and Sons Ltd
Bardi, F, Bet, B B, Pajkrt, E, Linskens, I H, Bekker, M N, Sistermans, E A, Bilardo, C M & Elvan-Taspinar, A 2022, ' Additional value of advanced ultrasonography in pregnancies with two inconclusive cell-free DNA draws ', Prenatal Diagnosis, vol. 42, no. 11, pp. 1358-1367 . https://doi.org/10.1002/pd.6238
Prenatal Diagnosis, 42(11), 1358-1367. John Wiley and Sons Ltd
Prenatal diagnosis, 42(11), 1358-1367. John Wiley and Sons Ltd
Bardi, F, Bet, B B, Pajkrt, E, Linskens, I H, Bekker, M N, Sistermans, E A, Bilardo, C M & Elvan-Taspinar, A 2022, ' Additional value of advanced ultrasonography in pregnancies with two inconclusive cell-free DNA draws ', Prenatal Diagnosis, vol. 42, no. 11, pp. 1358-1367 . https://doi.org/10.1002/pd.6238
Prenatal Diagnosis, 42(11), 1358-1367. John Wiley and Sons Ltd
Objective: We aimed to evaluate the additional value of advanced fetal anatomical assessment by ultrasound in pregnancies with twice inconclusive noninvasive testing (NIPT) due to low fetal fraction (FF).Methods: We performed a multicenter-retrospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d11983c45ac442f05f804857aad8cd5
https://research.rug.nl/en/publications/2461ac3c-beea-4393-925c-2b6f1e76e5b5
https://research.rug.nl/en/publications/2461ac3c-beea-4393-925c-2b6f1e76e5b5
Autor:
Malgorzata I. Srebniak, Olav Bjørn Petersen, Karin E. M. Diderich, Diane Van Opstal, Marike Polak, Maarten F. C. M. Knapen, Caterina M. Bilardo, Eric Smith, Lidia R. Arends, Ida Vogel
Publikováno v:
Petersen, O B, Smith, E, Van Opstal, D, Polak, M, Knapen, M F C M, Diderich, K E M, Bilardo, C M, Arends, L R, Vogel, I & Srebniak, M I 2020, ' Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review ', Acta Obstetricia et Gynecologica Scandinavica, vol. 99, no. 6, pp. 765-774 . https://doi.org/10.1111/aogs.13877
Acta Obstetricia et Gynecologica Scandinavica, 99(6), 765-774. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica
Acta Obstetricia et Gynecologica Scandinavica, 99(6), 765-774. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica
Introduction: Currently fetal nuchal translucency (NT) ≥3.5 mm is an indication for invasive testing often followed by chromosomal microarray. The aim of this study was to assess the risks for chromosomal aberrations in fetuses with an NT 3.0-3.4 m