Researcher
Linda De Meirleir
- Keywords:Medicine
Affiliations
- Pediatrics (Department)
Member
From1 Feb 2016 → 15 Oct 2018 - Clinical sciences (Department)
Member
From1 Jan 2014 → 31 Oct 2018 - Neurogenetics (Research group)
Responsible
From29 Jun 2011 → 31 Oct 2018 - Reproduction and Genetics (Research group)
Member
From21 Jun 2010 → 31 Oct 2018 - Pediatrics (Department)
Member
From1 Jan 2008 → 31 Oct 2018 - Pediatrics (Department)
Member
From1 Feb 1997 → 31 Dec 2013
Projects
1 - 1 of 1
- Development of diagnostic, biochemical and molecular methods, the prevention and the study of treatment of OXPHOS deficiency.From1 Jan 2010 → 31 Dec 2013Funding: FWO research project (including WEAVE projects)
Publications
21 - 30 of 63
- How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?(2016)
Authors: Charles Sèbiyo Batcho, Peter Y K Van den Bergh, Philip Van Damme, Anna J Roy, Jean-Louis Thonnard, Massimo Penta, Linda De Meirleir
Pages: 211-220 - Impact of age at onset and newborn screening on outcome in organic acidurias(2016)
Authors: Jana Heringer, Vassili Valayannopoulos, Allan Meldgaard Lund, Frits A Wijburg, Peter Freisinger, Ivo Barić, Matthias R Baumgartner, Peter Burgard, Alberto B Burlina, Kimberly A Chapman, et al.
Pages: 341-353 - Normal cognitive outcome in a PEX6 deficient girl despite neonatal multisystem presentation(2016)
Authors: Peter Witters, Luc Régal, Hans R Waterham, Linda De Meirleir, Ronald J A Wanders, Eva Morava
Pages: 1642-1646 - The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2(2015)
Authors: Stefan Kölker, Vassili Valayannopoulos, Alberto B Burlina, Jolanta Sykut-Cegielska, Frits A Wijburg, Elisa Leão Teles, Jirí Zeman, Carlo Dionisi-Vici, Ivo Barić, Daniela Karall, et al.
Pages: 1059-1074 - The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1(2015)
Authors: Stefan Kölker, Angeles Garcia-Cazorla, Vassili Valayannopoulos, Allan Meldgaard Lund, Alberto B Burlina, Jolanta Sykut-Cegielska, Frits A Wijburg, Elisa Leão Teles, Jirí Zeman, Carlo Dionisi-Vici, et al.
Pages: 1041-1057 - Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data(2015)
Authors: M. Huemer, C Bürer, Pavel Ješina, V Kožich, M A Landolt, T Suormala, B. Fowler, P Augoustides-Savvopoulou, E Blair, K Brennerova, et al.
Pages: 957-967 - Phenotypic plasticity and the perception-action-cognition-environment paradigm in neurodevelopmental genetic disorders(2015)
Authors: Bernard Dan, Karine Pelc, Linda De Meirleir, Guy Cheron
Pages: 52-54 - Eyes on MEGDEL(2015)
Authors: Saskia B Wortmann, Peter M van Hasselt, Ivo Barić, Alberto Burlina, Niklas Darin, Friederike Hörster, Mahmut Coker, Sema Kalkan Ucar, Zita Krumina, Karin Naess, et al.
Pages: 98-103 - Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2)(2015)
Authors: Arnaud V Vanlander, Björn Menten, Joél Smet, Linda De Meirleir, Tom Sante, Boel De Paepe, Sara Seneca, Sarah F Pearce, Christopher A Powell, Sarah Vergult, et al.
Pages: 222-231 - ALG11-CDG(2015)
Authors: Luc Régal, Peter M van Hasselt, F Foulquier, I Cuppen, Hcmt Prinsen, K Jansen, L Keldermans, Linda De Meirleir, G. Matthijs, J. Jaeken
Pages: 16-19