Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Liebaers, Ingeborg"'
Autor:
Belva, Florence, Hes, Frederik Jan, Tournaye, Herman, Bonduelle, Mary-Louise, Liebaers, Ingeborg, Verheyen, Greta, Van Steirteghem, Andre
Publikováno v:
Human Reproduction. 37
Intracytoplasmic sperm injection (ICSI), developed 30 years ago in our Center, allowed men with low to extremely low sperm quality to become the genetic father of their child. Overall, ICSI is now applied in up to 70% of all ART cycles and has result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ff39600bcf8afbe2d3ae9994fde0668
https://doi.org/10.1093/humrep/deac104.052
https://doi.org/10.1093/humrep/deac104.052
Publikováno v:
In Reproductive BioMedicine Online 2003 7(5):509-513
Autor:
Berckmoes, Veerle, Verdyck, Pieter, De Becker, Pascale, De Vos, Anick, Verheyen, Greta, Verpoest, Willem, Van der Niepen, Patricia, Liebaers, Ingeborg, Bonduelle, Maryse, De Rycke, Martine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::9fc572ca2e3d4e264214ad9df3d8f255
https://biblio.vub.ac.be/vubir/preimplantation-genetic-testing-for-polycystic-kidney-disease-is-an-option-for-affected-families(4a857692-8048-4a5f-9a27-ed9e2db73648).html
https://biblio.vub.ac.be/vubir/preimplantation-genetic-testing-for-polycystic-kidney-disease-is-an-option-for-affected-families(4a857692-8048-4a5f-9a27-ed9e2db73648).html
Autor:
Borry, Pascal, Cassiman, Jean-Jacques, Hulstaert, Frank, Liebaers, Ingeborg, Mortier, Geert, Peeters, Hilde, Van den Bulcke, Marc, Van Nerom, Anne, Van Oyen, Herman, Verellen-Dumoulin, Christine
status: published
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1131::5b3865a5855d99172bf964aaefdccddb
https://lirias.kuleuven.be/handle/123456789/579989
https://lirias.kuleuven.be/handle/123456789/579989
Autor:
De Paepe, Caroline, Cauffman, Greet, Verheyen, Greta, Dominic, Stoop, Liebaers, Ingeborg, Van De Velde, Hilde
Study question How are the trophectoderm (TE) key regulators CDX2, TEAD4 and YAP expressed during early human embryogenesis? Summary answer In human embryos, the restriction of TE-specific components to the TE occurs after expansion of the embryo, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::cc5e679b60c5c0980a17d4abfcf6c27b
https://biblio.vub.ac.be/vubir/differentiation-during-early-human-embryogenesis(59215ee7-af5b-4ef6-9a73-013422229f94).html
https://biblio.vub.ac.be/vubir/differentiation-during-early-human-embryogenesis(59215ee7-af5b-4ef6-9a73-013422229f94).html
Autor:
Van Dooren, Sonia, Endels, Kristof, Keymolen, Kathelijne, Seneca, Sara, Liebaers, Ingeborg, Lissens, Willy
Background: Hemoglobinopathies are common monogenic diseases forming a major public health problem due to their severity and disabling nature. Genetic identification of the two most frequently observed missense mutations in the beta-globin gene, HbS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::af4893c583f5a146318925ec0ed3c1a1
https://biblio.vub.ac.be/vubir/rapid-sensitive-and-discriminatory-hbs-and-hbc-mutation-detection-using-high-resolution-melting-analysis(5c279976-e110-43e2-a6b4-0019f8703551).html
https://biblio.vub.ac.be/vubir/rapid-sensitive-and-discriminatory-hbs-and-hbc-mutation-detection-using-high-resolution-melting-analysis(5c279976-e110-43e2-a6b4-0019f8703551).html
no abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::93a86eb548c03c43ceebf5cc7bfa5976
https://biblio.vub.ac.be/vubir/preimplantation-genetic-diagnosis-of-reduced-penetrance-alleles-in-huntingtons-disease-controversial-but-morally-justified(81d03502-dfab-4624-bbf1-47f86b8c815d).html
https://biblio.vub.ac.be/vubir/preimplantation-genetic-diagnosis-of-reduced-penetrance-alleles-in-huntingtons-disease-controversial-but-morally-justified(81d03502-dfab-4624-bbf1-47f86b8c815d).html
Autor:
De Rademaeker, Marjan, Moutou, Céline, Van Rij, Maartje, Dreesen, J., De Rycke, Martine, Liebaers, Ingeborg, Viville, Stéphane, Geraedts, J., De Die, Christine
No abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::c7500f507cb5cd13d09a61d4053af2b0
https://biblio.vub.ac.be/vubir/the-combined-experience-of-three-european-centres-with-preimplantation-genetic-diagnosis-for-huntington-disease(d6b57257-b9b0-4af9-9ca4-14c38817fc8d).html
https://biblio.vub.ac.be/vubir/the-combined-experience-of-three-european-centres-with-preimplantation-genetic-diagnosis-for-huntington-disease(d6b57257-b9b0-4af9-9ca4-14c38817fc8d).html
Autor:
De Rycke, Martine, Verpoest, Willem, De Becker, Pascale, Van De Velde, Hilde, Liebaers, Ingeborg, Bonduelle, Mary-Louise
Cartilage-hair hypoplasia (CHH) is a rare autosomal recessive disorder, characterised by dwarfism, hypoplastic hair and immunodeficiency. Allogeneic hematopoietic stem cell transplantation (HSCT) has been shown to be an effective treatment for CHH pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::2192eee26b2aaa6df8425b812060c163
https://biblio.vub.ac.be/vubir/preimplantation-genetic-diagnosis-pgd-for-cartilage-hair-hypopasia-combined-with-human-leukocyte-antigen-hla(f70996be-6bcd-4401-86b7-f332e6b634ce).html
https://biblio.vub.ac.be/vubir/preimplantation-genetic-diagnosis-pgd-for-cartilage-hair-hypopasia-combined-with-human-leukocyte-antigen-hla(f70996be-6bcd-4401-86b7-f332e6b634ce).html
Autor:
Seneca, Sara, Smet, J., Vancoster, R., Van Dooren, Sonia, Lissens, Willy, Bonduelle, Mary-Louise, Liebaers, Ingeborg, De Meirleir, Linda
Mitochondrial DNA (mtDNA) copy number reduction, known as the mitochondrial DNA depletion syndrome (MDS), is a common cause of severe mitochondrial disorders of infancy and early childhood. MDS results from defects in nuclear encoded factors involved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::599ac8518bb96e89959cf5b1124eeca1
https://biblio.vub.ac.be/vubir/deleterious-mutations-in-rrm2b-causing-severe-mitochondrial-dna-depletion-in-infancy(9b6e053d-7a11-4221-b240-196980bbbedd).html
https://biblio.vub.ac.be/vubir/deleterious-mutations-in-rrm2b-causing-severe-mitochondrial-dna-depletion-in-infancy(9b6e053d-7a11-4221-b240-196980bbbedd).html