Zobrazeno 1 - 10
of 19
pro vyhledávání: '"G. C. M. L. Page-Christiaens"'
Autor:
R. Hochstenbach, G. C. M. L. Page-Christiaens, A. C. C. van Oppen, K. D. Lichtenbelt, J. J. T. van Harssel, T. Brouwer, G. T. R. Manten, P. van Zon, M. Elferink, K. Kusters, O. Akkermans, J. K. Ploos van Amstel, G. H. Schuring-Blom
Publikováno v:
Case Reports in Genetics, Vol 2015 (2015)
Noninvasive prenatal testing (NIPT) validation studies show high sensitivity and specificity for detection of trisomies 13, 18, and 21. False negative cases have rarely been reported. We describe a false negative case of trisomy 13 and another of tri
Externí odkaz:
https://doaj.org/article/a38909954ee340b2a7d4715161c46828
Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes
Autor:
Ahmad Javadi, Anneke Kwee, Marije Lamain – de Ruiter, G. C. M. L. Page-Christiaens, Maria P.H. Koster, Arie Franx, Heleen Woortmeijer, Florentine F. Thurik, C. Ellen van der Schoot
Publikováno v:
Prenatal Diagnosis. 36:1104-1111
OBJECTIVE: To study associations of first trimester cell-free fetal DNA levels (in this paper referred to as cell-free placental DNA (cfpDNA) levels) and preeclampsia (PE), pregnancy-induced hypertension (PIH), gestational diabetes (GDM) and spontane
Autor:
Ron Hochstenbach, Klaske D. Lichtenbelt, Jeske J.T. van Harssel, Martin G Elferink, Patrick H.A. van Zon, G. C. M. L. Page-Christiaens, Heleen Schuring-Blom
Publikováno v:
Clinical case reports, 6(5), 788. John Wiley and Sons Ltd
Clinical Case Reports
Clinical Case Reports
Key Clinical Message One of the confounders in noninvasive prenatal testing (NIPT) is the vanishing twin phenomenon. Prolonged contribution to the maternal Cell‐free DNA (cfDNA) pool by cytotrophoblasts representing a demised, aneuploid cotwin may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4755dad5d7ccdbda01b61a32a200ccd
https://dspace.library.uu.nl/handle/1874/365151
https://dspace.library.uu.nl/handle/1874/365151
Autor:
G. C. M. L. Page-Christiaens, Bernadette Bossers, M. de Haas, C. E. Van Der Schoot, Heleen Woortmeijer, Florentine F. Thurik, A. Ait Soussan, Barbera Veldhuisen
Publikováno v:
Prenatal Diagnosis. 35:754-760
Objectives We aim to elucidate causes of false-positive fetal RHD screening results obtained with cell-free DNA. Methods Fetal RHD screening was performed in 32 222 samples from RhD-negative women by multiplex real-time PCR in triplicate for RHD exon
Autor:
J. Siljee, Klaske D. Lichtenbelt, G. H. Schuring-Blom, B. D. M. Diemel, Maria P.H. Koster, G. C. M. L. Page-Christiaens, Gwendolyn T. R. Manten
Publikováno v:
Prenatal Diagnosis. 35:663-668
Objectives The objective of this study is to determine what percentage of fetal chromosomal anomalies remains undetected when first trimester combined testing is replaced by non-invasive prenatal testing for trisomies 13, 18, and 21. We focused on th
Autor:
A. Ait Soussan, O. J. H. M. Verhagen, C. E. Van Der Schoot, M. de Haas, P. G. Scheffer, G. C. M. L. Page-Christiaens, Dick Oepkes
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 118:1392-1395
Please cite this paper as: Scheffer P, Ait Soussan A, Verhagen O, Page-Christiaens G, Oepkes D, de Haas M, van der Schoot C. Noninvasive fetal genotyping of human platelet antigen-1a. BJOG 2011;118:1392–1395. We describe a reliable noninvasive feta
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 118:1340-1348
Please cite this paper as: Scheffer P, van der Schoot C, Page-Christiaens G, de Haas M. Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience. BJOG 2011;118:134
Autor:
Joke A. M. Hunfeld, J.J.H.M. Erwich, M.J. Korenromp, C.M.A.A. Potters, Eduard J. H. Mulder, G. C. M. L. Page-Christiaens, J. R. Beekhuis, J.T.J. Brons, C.J.M. van Binsbergen, J. van den Bout, Gerhard Henk Visser, A.W.J. Omtzigt
Publikováno v:
Prenatal Diagnosis, 27(8), 709-716. John Wiley & Sons Ltd.
Prenatal Diagnosis, 27(8), 709-716. Wiley-Blackwell
Prenatal Diagnosis, 27(8), 709-716. Wiley-Blackwell
Objective To identify short-term factors influencing psychological outcome of termination of pregnancy for fetal anomaly, in order to define those patients most vulnerable to psychopathology.Study Design A prospective cohort of 217 women and 169 men
Publikováno v:
Clinical genetics. 89(5)
The practice of prenatal screening is undergoing important changes as a result of the introduction of genomic testing technologies at different stages of the screening trajectory. It is expected that eventually it will become possible to routinely ob
Autor:
F F, Thurik, A, Ait Soussan, B, Bossers, H, Woortmeijer, B, Veldhuisen, G C M L, Page-Christiaens, M, de Haas, C E, van der Schoot
Publikováno v:
Prenatal diagnosis. 35(8)
We aim to elucidate causes of false-positive fetal RHD screening results obtained with cell-free DNA.Fetal RHD screening was performed in 32,222 samples from RhD-negative women by multiplex real-time PCR in triplicate for RHD exons 5 and 7 using cell