Researcher
Alexander Gheldof
- Keywords:Medicine
- Disciplines:Other basic sciences not elsewhere classified
Affiliations
- Neurogenetics (Research group)
Member
From15 Apr 2015 → Today - Medical Genetics (Department)
Member
From1 Jan 2014 → Today - Clinical sciences (Department)
Member
From1 Feb 2021 → Today - Clinical sciences (Department)
Member
From1 Feb 2021 → 20 Oct 2022 - Clinical sciences (Department)
Member
From17 Feb 2020 → Today - Clinical sciences (Department)
Member
From17 Feb 2020 → 20 Oct 2022 - Basic (bio-) Medical Sciences (Department)
Member
From15 Apr 2015 → 14 Apr 2017
Publications
1 - 10 of 21
- The Diagnostic and Therapeutic Challenges of Fabry Nephropathy—A Review of the Literature, Illustrated by a Clinical Case(2023)
Authors: Stefan Eric Van Cauwelaert, Caroline Geers, Dominique Vandervelde, Esther Scheirlynck, Alexander Gheldof, Karl Martin Wissing
Pages: 349-360 - A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development(2023)
Authors: 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.
Pages: 218-232 - EDIR(2023)
Authors: 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)
Authors: 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)
Authors: 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)
Authors: Kaoutar Tazi, Vanessa Guy-Viterbo, Alexander Gheldof, Aurélie Empain, Anne Paternoster, Corinne De Laet
Pages: 316-321 - Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder(2022)
Authors: 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.
Pages: 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)
Authors: 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)
Authors: 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)
Authors: Christina Markouli, Edouard Couvreu De Deckersberg, Dominika Alicja Dziedzicka, Marius Regin, Silvie Franck, Alexander Scott Keller, Alexander Gheldof, Mieke Geens, Karen Sermon, C Spits