Zobrazeno 1 - 10
of 106
pro vyhledávání: '"CHRISTIAENS, G. C. M. L."'
Autor:
Van Der Sijs-Bos, C. J. M., Stigter, R. H., Christiaens, G. C. M. L., Leschot, N. J., Gravholt, Claus Højbjerg, Juul, Svend, Naeraa, Rune Weis
Publikováno v:
BMJ: British Medical Journal, 1996 Jul 01. 313(7048), 47-48.
Externí odkaz:
https://www.jstor.org/stable/29732202
Autor:
Hochstenbach, R.1 p.f.r.hochstenbach@umcutrecht.nl, Page-Christiaens, G. C. M. L.2 l.christiaens@umcutrecht.nl, van Oppen, A. C. C.2 a.c.c.vanoppen@umcutrecht.nl, Lichtenbelt, K. D.1 k.d.lichtenbelt@umcutrecht.nl, van Harssel, J. J. T.1 j.vanharssel@umcutrecht.nl, Brouwer, T.1 tbrouwer@umcutrecht.nl, Manten, G. T. R.2 g.t.r.manten@umcutrecht.nl, van Zon, P.1 p.h.a.vanzon@umcutrecht.nl, Elferink, M.1 m.elferink@umcutrecht.nl, Kusters, K.1 k.kusters@umcutrecht.nl, Akkermans, O.1 o.d.akkermans-2@umcutrecht.nl, Ploos van Amstel, J. K.1 j.k.ploosvanamstel@umcutrecht.nl, Schuring-Blom, G. H.1 g.h.schuring-blom@umcutrecht.nl
Publikováno v:
Case Reports in Genetics. 6/7/2015, Vol. 2015, p1-7. 7p.
Autor:
Dutch Study Group On Prevention Of Neonatal Hepatitis, Grosheide, P. M., Waldimiroff, J. W., Heijtink, R. A., Mazel, J. A., Christiaens, G. C. M. L., Nuijten, A. S. M., Schalm, S. W.
Publikováno v:
BMJ: British Medical Journal, 1995 Nov 01. 311(7014), 1197-1199.
Externí odkaz:
https://www.jstor.org/stable/29729365
Publikováno v:
Clinical Genetics, 89(5). Wiley
Clinical Genetics, 89(5), 531. Wiley-Blackwell
Clinical Genetics, 89(5), 531. Wiley-Blackwell
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3981211f8ad56cd2f02e36d00f74b7a0
https://cris.maastrichtuniversity.nl/en/publications/6750d580-b4e0-4fff-bf7e-1ddda8106514
https://cris.maastrichtuniversity.nl/en/publications/6750d580-b4e0-4fff-bf7e-1ddda8106514
Autor:
Lichtenbelt, K. D., Diemel, B. D M, Koster, M. P H, Manten, G. T R, Siljee, J., Schuring-Blom, G. H., Page-Christiaens, G. C M L
Publikováno v:
Prenatal Diagnosis, 35(7), 663. John Wiley and Sons Ltd
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 t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fb3c7c77584fa7ae501297b8f0ab5518
https://dspace.library.uu.nl/handle/1874/331313
https://dspace.library.uu.nl/handle/1874/331313
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 159. Bohn Stafleu van Loghum
The non-invasive prenatal test (NIPT) is an accurate and safe test in which blood from the pregnant woman is used to investigate if the unborn child possibly has trisomy 21 (Down's syndrome), trisomy 18 (Edwards' syndrome) or trisomy 13 (Patau syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::6659f68cc9bcd67a04d80a2994282651
https://research.vumc.nl/en/publications/27b03acc-9795-4656-93f1-60c022cd6072
https://research.vumc.nl/en/publications/27b03acc-9795-4656-93f1-60c022cd6072
Autor:
Thurik, F. F., Ait Soussan, A., Bossers, B., Woortmeijer, H., Veldhuisen, B., Page-Christiaens, G. C M L, de Haas, M., van der Schoot, C. E.
Publikováno v:
Prenatal diagnosis, 35(8), 754-760. John Wiley and Sons Ltd
Prenatal Diagnosis, 35(8), 754. John Wiley and Sons Ltd
Prenatal Diagnosis, 35(8), 754. John Wiley and Sons Ltd
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 32222 samples from RhD-negative women by multiplex real-time PCR in triplicate for RHD exons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b2ad211502c5608c486a760bbee7f3b4
https://pure.amc.nl/en/publications/analysis-of-falsepositive-results-of-fetal-rhd-typing-in-a-national-screening-program-reveals-vanishing-twins-as-potential-cause-for-discrepancy(6ebec043-f32e-453b-9af7-b83598cfd010).html
https://pure.amc.nl/en/publications/analysis-of-falsepositive-results-of-fetal-rhd-typing-in-a-national-screening-program-reveals-vanishing-twins-as-potential-cause-for-discrepancy(6ebec043-f32e-453b-9af7-b83598cfd010).html
Publikováno v:
Henneman, L, Page-Christiaens, G C M L L & Oepkes, D 2015, ' NIPT, de niet-invasieve prenatale test : uitdagingen voor de toekomst ', Nederlands Tijdschrift voor Geneeskunde, vol. 159, pp. A9479 .
The non-invasive prenatal test (NIPT) is an accurate and safe test in which blood from the pregnant woman is used to investigate if the unborn child possibly has trisomy 21 (Down's syndrome), trisomy 18 (Edwards' syndrome) or trisomy 13 (Patau syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10172::748103e0aa560261f310d2119d9129ef
https://research.vumc.nl/en/publications/27b03acc-9795-4656-93f1-60c022cd6072
https://research.vumc.nl/en/publications/27b03acc-9795-4656-93f1-60c022cd6072
Autor:
Mulder, E. J. H., Versteegh, E. M. J., Bloemenkamp, K. W. M., Lim, A. C., Mol, B. W. J., Bekedam, D. J., Kwee, A., Bruinse, H. W., Christiaens, G. C. M. L.
Publikováno v:
Ultrasound in obstetrics & gynecology, 42(3), 329-334. John Wiley and Sons Ltd
Increasingly, maternal administration of 17-α-hydroxyprogesterone caproate (17-OHPC) is utilized to prevent preterm birth, but the fetal safety of 17-OHPC is still a matter of concern. This study aimed to assess whether exposure to 17-OHPC during th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::70a6bf1f2b4d5bfe2ecb06bddc0b67c2
https://pure.amc.nl/en/publications/does-17hydroxyprogesterone-caproate-affect-fetal-biometry-and-birth-weight-in-twin-pregnancy(eecae70e-941c-4746-9e4b-b3e188f496a7).html
https://pure.amc.nl/en/publications/does-17hydroxyprogesterone-caproate-affect-fetal-biometry-and-birth-weight-in-twin-pregnancy(eecae70e-941c-4746-9e4b-b3e188f496a7).html
Publikováno v:
BJOG, 118(11), 1340-1348. Wiley-Blackwell
To evaluate the diagnostic performance of noninvasive fetal blood group genotyping. Descriptive analysis. Dutch national reference laboratory for pregnancies complicated by alloimmunisation. All consecutive alloimmunised pregnant women for whom fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::96ddff5ec8eff82f3a93e2b274e10d50
https://pure.amc.nl/en/publications/noninvasive-fetal-blood-group-genotyping-of-rhesus-d-c-e-and-of-k-in-alloimmunised-pregnant-women-evaluation-of-a-7year-clinical-experience(16a2a8da-218b-4365-aac4-1dd62672e10f).html
https://pure.amc.nl/en/publications/noninvasive-fetal-blood-group-genotyping-of-rhesus-d-c-e-and-of-k-in-alloimmunised-pregnant-women-evaluation-of-a-7year-clinical-experience(16a2a8da-218b-4365-aac4-1dd62672e10f).html