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Onderzoeker
Elise Vantroys
- Disciplines:Endocrinologie en metabole ziekten, Pediatrie en neonatologie, Verpleegkunde
Affiliaties
- Vakgroep Inwendige ziekten en Pediatrie (Departement)
Lid
Vanaf1 okt 2018 → 22 sep 2019 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 dec 2014 → 30 sep 2018
Publicaties
1 - 5 van 5
- Mitochondria lost in translation : mitochondrial DNA translation defects caused by nuclear gene deficiencies(2019)
Auteurs: Elise Vantroys
- Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C > T mutation in MTFMT(2018)
Auteurs: Dimitri Hemelsoet, Arnaud Vanlander, Joél Smet, Elise Vantroys, Marjan Acou, Ingeborg Goethals, Tom Sante, Sara Seneca, Björn 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 Vanlander, Sarah Vergult, Ruth De Bruyne, Hedwig Stepman, Herbert Roeyers
- New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disordersVolume: 123
Auteurs: Kaz Knight, Marisa W Friederich, Rudy Van Coster, Joél Smet, Elise Vantroys, Michio Hirano, Amy Goldstein, Johan LK Van Hove
Pagina's: 202 - 202 - Subcomplexes of complex V in a patient with Perrault syndrome due to pathogenic mutations in C10orf2Volume: 39
Auteurs: PATRICK VERLOO, Joél Smet, Elise Vantroys, Arnaud Vanlander, Sarah Vergult, Tom Sante, Rudy Van Coster
Pagina's: S164 - S164