Zobrazeno 1 - 10
of 430
pro vyhledávání: '"Staessen, C"'
Publikováno v:
In Reproductive BioMedicine Online 2006 12(3):334-339
Autor:
De Rycke, M., Staessen, C.
Publikováno v:
In Molecular Diagnostics Edition: Third Edition. 2017:407-421
STUDY QUESTION: Does preimplantation genetic testing for aneuploidy (PGT-A) by comprehensive chromosome screening (CCS) of the first and second polar body to select embryos for transfer increase the likelihood of a live birth within 1 year in advance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f66445c1e2276e4a85df51edee2c0a4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3107086
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3107086
Autor:
Devroey P., Fauser B. C., Diedrich K., Baart E., Barrat C., Bergh C., Broekmans F., Evers J. L., Griesinger G., Keay S., Olivennes F., Serour G., Staessen C., Sunde A., Venetis C., Yarali H., Howles C. M., Jenkins J., ALVIGGI, CARLO
Publikováno v:
Human Reproduction Update
Human Reproduction Update, 15(4), 391-408. Oxford University Press
Human Reproduction Update, 15(4), 391-408. Oxford University Press
BACKGROUND Recent advances in our understanding of the causes of infertility and of assisted reproductive technology (ART) have led to the development of complex diagnostic tools, prognostic models and treatment options. The Third Evian Annual Reprod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1505768742822eb0a006735652f8bec
http://hdl.handle.net/11588/376845
http://hdl.handle.net/11588/376845
Autor:
Vanneste, E., Melotte, Cindy, Ullmann, Urielle, Staessen, C., Liebaers, Ingeborg, Voet, Thierry, Debrock, S, D'hooghe, T., Vermeesch, Joris
Preimplantation genetic diagnosis (PGD) is the genetic analysis of a single (or two) blastomere(s) from an in vitro fertilized embryo and is offered to couples to avoid the transmission of heritable genetic disorders to their potential offspring. Flu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::30e3ce2e5ccd9819bf89ee435ad0868e
https://biblio.vub.ac.be/vubir/replacement-of-fish-by-genomewide-single-cell-array-analysis-for-preimplantation-genetic-diagnosis-of-translocation-carriers(a795d7dd-c3cf-4b37-b27a-4f1d24385016).html
https://biblio.vub.ac.be/vubir/replacement-of-fish-by-genomewide-single-cell-array-analysis-for-preimplantation-genetic-diagnosis-of-translocation-carriers(a795d7dd-c3cf-4b37-b27a-4f1d24385016).html
Autor:
Mertzanidou, Afroditi, Wilton, Leeanda, Spits, Claudia, Vanneste, E., Staessen, C., Mcbain, J., Liebaers, Ingeborg, Vermeesch, Joris, Sermon, Karen
Introduction: Fluorescent in situ hybridization (FISH) is currently the main method used for aneuploidy preimplantation genetic screening (PGS). The main limitation of FISH analysis is that it usually includes only 5-10 chromosome- specific probes, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::2bdeb03e2783042dfc0f13ebe8a758f3
https://biblio.vub.ac.be/vubir/molecular-karyotyping-by-arraycgh-on-single-blastomeres-a-pilot-study(425a1484-ca4d-4068-9394-b54109753c83).html
https://biblio.vub.ac.be/vubir/molecular-karyotyping-by-arraycgh-on-single-blastomeres-a-pilot-study(425a1484-ca4d-4068-9394-b54109753c83).html
Autor:
Desmyttere, Sonja, De Schepper, Jean, Nekkebroeck, Julie, De Vos, A., De Rycke, Martine, Staessen, C., Liebaers, Ingeborg, Bonduelle, Mary-Louise
no abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::db822b8e60249433403c0c7a40af2868
https://hdl.handle.net/20.500.14017/e8866ac9-871c-4b4a-a1cc-48cf6adc2eb6
https://hdl.handle.net/20.500.14017/e8866ac9-871c-4b4a-a1cc-48cf6adc2eb6
Autor:
Donoso, P, Verpoest, W, Papanikolaou, E G, Liebaers, I, Fatemi, H M, Sermon, K, Staessen, C, Van der Elst, J, Devroey, P
BACKGROUND: The Belgian legislation imposes single embryo transfer (SET) on women of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::72e4f0475fdd51fce5846b6566fab06e
https://biblio.vub.ac.be/vubir/single-embryo-transfer-in-preimplantation-genetic-diagnosis-cycles-for-women(510ce2f5-cd9f-42a8-87ef-f55b50349dfb).html
https://biblio.vub.ac.be/vubir/single-embryo-transfer-in-preimplantation-genetic-diagnosis-cycles-for-women(510ce2f5-cd9f-42a8-87ef-f55b50349dfb).html
Aim of the study. In this study we characterize the pregnancies with cytogenetic diagnosis of trisomy 21. Materials and methods. We retrospectively looked at pregnancies in which trisomy 21 was found in chorionic villus sampling (CVS) or amniocentesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::b634685af12536eab8e85709d6daf793
https://biblio.vub.ac.be/vubir/characteristics-of-pregnancies-with-cytogenetic-diagnosis-of-trisomy-21(adfbc569-77a1-4628-98ed-54b229981ef7).html
https://biblio.vub.ac.be/vubir/characteristics-of-pregnancies-with-cytogenetic-diagnosis-of-trisomy-21(adfbc569-77a1-4628-98ed-54b229981ef7).html
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