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Researcher
Elise Vantroys
- Disciplines:Endocrinology and metabolic diseases, Paediatrics and neonatology, Nursing
Affiliations
- Department of Internal Medicine and Pediatrics (Department)
Member
From1 Oct 2018 → 22 Sep 2019 - Department of Pediatrics and medical genetics (Department)
Member
From1 Dec 2014 → 30 Sep 2018
Publications
1 - 5 of 5
- Mitochondria lost in translation : mitochondrial DNA translation defects caused by nuclear gene deficiencies(2019)
Authors: Elise Vantroys
- Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C > T mutation in MTFMT(2018)
Authors: 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)
Authors: 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
Authors: Kaz Knight, Marisa W Friederich, Rudy Van Coster, Joél Smet, Elise Vantroys, Michio Hirano, Amy Goldstein, Johan LK Van Hove
Pages: 202 - 202 - Subcomplexes of complex V in a patient with Perrault syndrome due to pathogenic mutations in C10orf2Volume: 39
Authors: PATRICK VERLOO, Joél Smet, Elise Vantroys, Arnaud Vanlander, Sarah Vergult, Tom Sante, Rudy Van Coster
Pages: S164 - S164