Onderzoeker
Alexander Gheldof
- Trefwoorden:Geneeskunde
- Disciplines:Andere basiswetenschappen niet elders geclassificeerd
Affiliaties
- Neurogenetica (Onderzoeksgroep)
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Vanaf15 apr 2015 → Heden - Medische genetica (Departement)
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Vanaf1 jan 2014 → Heden - Observerende Klinische wetenschappen (Departement)
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Vanaf1 feb 2021 → Heden - Observerende Klinische wetenschappen (Departement)
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Vanaf1 feb 2021 → 20 okt 2022 - Observerende Klinische wetenschappen (Departement)
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Vanaf17 feb 2020 → Heden - Observerende Klinische wetenschappen (Departement)
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Vanaf17 feb 2020 → 20 okt 2022 - Basis (bio)-medische wetenschappen (Departement)
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Vanaf15 apr 2015 → 14 apr 2017
Publicaties
1 - 10 van 21
- The Diagnostic and Therapeutic Challenges of Fabry Nephropathy—A Review of the Literature, Illustrated by a Clinical Case(2023)
Auteurs: Stefan Eric Van Cauwelaert, Caroline Geers, Dominique Vandervelde, Esther Scheirlynck, Alexander Gheldof, Karl Martin Wissing
Pagina's: 349-360 - A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development(2023)
Auteurs: Annelore Van Der Kelen, Özlem Okutman, Elodie Javey, Münevver Serdarogullari, Charlotte Janssens, Manjusha S Ghosh, Bart J H Dequeker, Florence Perold, Claire Kastner, Emmanuelle Kieffer, et al.
Pagina's: 218-232 - EDIR(2023)
Auteurs: D.T. Laura Vo Ngoc, Randy Osei, Katrin Dohr, Catharina Olsen, Sara Seneca, Alexander Gheldof
- The genetic diagnosis of rare endocrine disorders of sex development and maturation(2022)
Auteurs: Luca Persani, Martine Cools, Stamatina Ioakim, S Faisal Ahmed, Silvia Andonova, Magdalena Avbelj-Stefanija, Federico Baronio, Jerome Bouligand, Hennie T Bruggenwirth, Justin H Davies, et al.
- Case report(2022)
Auteurs: Ann Cordenier, Anja Flamez, Thomy de Ravel, Alexander Gheldof, Luigi Pannone, Carlo de Asmundis, Gudrun Pappaert, Véronique Bissay
- Ascites in infantile onset type II Sialidosis(2022)
Auteurs: Kaoutar Tazi, Vanessa Guy-Viterbo, Alexander Gheldof, Aurélie Empain, Anne Paternoster, Corinne De Laet
Pagina's: 316-321 - Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder(2022)
Auteurs: Nuno M. M. Maia, Sven Potelle, Hamide Yildirim, Sandrine Duvet, Shyam K. Akula, Celine Schulz, Elsa Wiame, Alexander Gheldof, Katherine O'kane, Abbe Lai, et al.
Pagina's: 345-360 - Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing(2022)
Auteurs: Silvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, Christina Markouli, Lise Barbé, Joke Allemeersch, Pierre Hilven, Geoffrey Duqué, Maurice S Swanson, Alexander Gheldof, et al.
- Intra-amniotic levothyroxine infusions in a case of fetal goiter due to novel Thyroglobulin gene variants(2021)
Auteurs: Olivier G Pollé, Alexander Gheldof, Philippe A Lysy, Pierre Bernard
- Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm(2021)
Auteurs: Christina Markouli, Edouard Couvreu De Deckersberg, Dominika Dziedzicka, Marius Regin, Silvie Franck, Alexander Keller, Alexander Gheldof, Mieke Geens, Karen Sermon, Claudia Spits