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
41 - 50 of 63
- Air leaks localized with lung ventilation SPECT(2012)
Authors: Gaëtane Ceulemans, Linda De Meirleir, Douwe Erwin Verdries, Walter Vincken
Pages: 1182-1183 - Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.(2010)
Authors: Yasmin Namavar, P.g. Barth, Paul Kasher, Fred Van Ruiiiissen, Knut Brockmann, Günther Bernert, Karin Wriiiitzlll, Edith Cheng, Donna Ferriiiiero, Lina Basellll-Vanagaiiiite, et al.
Pages: 143-156 - Mutations in PEX10 are a cause of autosomal recessive ataxia.(2010)
Authors: Luc Régal, M. Ebberink, Nathalie Goemans, R.j.a. Wanders, Linda De Meirleir, J. Jaeken, Maarten Schrooten, R. Vancoster, H. Waterham
Pages: 259-263 - Mutations in TMEM70 causes severe encephalocardiomyopathy as well as mild encephalopathy(2010)
Authors: R. Vancoster, Joél Smet, Willy Lissens, Boél De Paepe, Sara Seneca, Linda De Meirleir, M. Spilioti, X. Fitsioris, A. Evangeliou
Pages: 85-85 - Deleterious mutations in RRM2B result in severe reduction of mtDNA content in skeletal muscle(2010)
Authors: R. Vancoster, Joél Smet, Boél De Paepe, Willy Lissens, Linda De Meirleir, Sara Seneca
Pages: 86-86 - LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood.(2010)
Authors: Caroline Michot, Laurence Hubert, Linda De Meirleir, Vassili Valayannopoulos, Wolfgang Müller-Felber, Ramesh Venkateswaran, Hélène Ogier, Isabelle Desguerre, Cécilia Altuzarra, Elisabeth Thompson, et al.
Pages: 1564-1573 - Home treatment with intravenous enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II - data from the Hunter Outcome Survey.(2010)
Authors: Bk. Burton, N. Guffon, J. Roberts, Ans Van Der Ploeg, Simon Jones, Linda De Meirleir, Hos Investigators
Pages: 123-129 - Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome
due to m.14487T>C.(2010)
Authors: Bart Dermaut, Sara Seneca, L. Dom, Joél Smet, Boél De Paepe, S. Tousseyn, S. Weckhuysen, M. Gewillig, P. Pals, Paul Parizel, et al.
Pages: 90-93 - Effect of ankle-foot orthoses on gait in typically developing children: Developmental trend in segmental coordination(2010)
Authors: M Degelaen, Eric Kerckhofs, Linda De Meirleir, Bernard Dan, Ludo De Borre, G Cheron, F Leurs
Pages: 163-170 - Mutational study in the PDHA1 gene of 40 patients suspected of pyruvate dehydrogenase
complex deficiency.(2010)
Authors: E. Quintana, L. Gort, C. Busquets, A. Navarro-Sastre, Willy Lissens, S. Moliner, M. Lluch, Ma. Vilaseca, Linda De Meirleir, A. Ribes, et al.
Pages: 474-482