Onderzoeker
Elise Vantroys
- Trefwoorden:Geneeskunde
- Disciplines:Klinische genetica en moleculaire diagnostiek
Affiliaties
- Medische genetica (Departement)
Lid
Vanaf1 jan 2019 → Heden - Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 okt 2019 → Heden - Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 okt 2019 → 20 okt 2022
Publicaties
1 - 6 van 6
- Urine lactate concentration as a non-invasive screener for metabolic abnormalities(2022)
Auteurs: Sofie Boterberg, Elise Vantroys, Boel De Paepe, Rudy Van Coster, Herbert Roeyers
- Outcome of publicly funded nationwide first-tier noninvasive prenatal screening(2021)
Auteurs: Kris Van den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener, et al.
Pagina's: 1137-1142 - Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations(2021)
Auteurs: Margot van Riel, Nathalie Brison, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Saskia Bulk, Anne De Leener, Julie Désir, Koenraad Devriendt, et al.
Pagina's: 1102-1108 - Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in MTFMT(2018)
Auteurs: Dimitri M Hemelsoet, Arnaud V Vanlander, Joél Smet, Elise Vantroys, Marjan Acou, Ingeborg Goethals, Tom Sante, Sara Seneca, Bjorn Menten, Rudy Van Coster
- Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency(2018)
Auteurs: Elise Vantroys, Joél Smet, Arnaud V Vanlander, Sarah Vergult, Ruth De Bruyne, Frank Roels, Hedwig Stepman, Herbert Roeyers, Björn Menten, Rudy Van Coster
- New insights into the phenotype of FARS2 deficiency(2017)
Auteurs: Elise Vantroys, Austin Larson, Marisa W Friederich, Kaz Knight, Michael A Swanson, Christopher A Powell, Joél Smet, Sarah Vergult, Boel De Paepe, Sara Seneca, et al.
Pagina's: 172-181