Onderzoeker
Linda De Meirleir
- Trefwoorden:Geneeskunde
Affiliaties
- Pediatrie (kind) (Departement)
Lid
Vanaf1 feb 2016 → 15 okt 2018 - Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 jan 2014 → 31 okt 2018 - Neurogenetica (Onderzoeksgroep)
Verantwoordelijke
Vanaf29 jun 2011 → 31 okt 2018 - Reproductie en Genetica (Onderzoeksgroep)
Lid
Vanaf21 jun 2010 → 31 okt 2018 - Pediatrie (kind) (Departement)
Lid
Vanaf1 jan 2008 → 31 okt 2018 - Pediatrie (Departement)
Lid
Vanaf1 feb 1997 → 31 dec 2013
Projecten
1 - 1 of 1
- Ontwikkeling van diagnostische, biochemische en moleculaire methoden, de preventie en de studie van behandelingsmogelijkheden bij OXPHOS deficiënties.Vanaf1 jan 2010 → 31 dec 2013Financiering: FWO Onderzoeksproject (incl. WEAVE projecten)
Publicaties
31 - 40 van 63
- Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?(2015)
Auteurs: Sara Seneca, Kim Vancampenhout, Rudy Van Coster, Joél Smet, Willy Lissens, A. Vanlander, Boel De Paepe, An Jonckheere, Katrien Stouffs, Linda De Meirleir
Pagina's: 41-48 - Early treatment of a child with NAGS deficiency using N-carbamyl glutamate results in a normal neurological outcome(2014)
Auteurs: Anouk Van Leynseele, Anna C Jansen, Philippe Goyens, Geert Martens, S. Peeters, An Jonckheere, Linda De Meirleir
Pagina's: 1635-1638 - Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: Improved survival by prompt diagnosis.(2014)
Auteurs: E. Scalais, Jean Bottu, R.j.a. Wanders, H. Waterham, Sacha Ferdinandusse, Linda De Meirleir
Pagina's: 211-214 - Congenital mirror movements(2014)
Auteurs: Aurélie Méneret, Christel Depienne, Florence Riant, Oriane Trouillard, Delphine Bouteiller, Massimo Cincotta, Pierre Bitoun, Julia Wickert, Isabelle Lagroua, Ana Westenberger, et al.
Pagina's: 1999-2002 - Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature(2014)
Auteurs: Caroline De Bruyn, Tim Vanderhasselt, Ibrahim Tanyalcin, K. Keymolen, Katrijn Van Rompaey, Linda De Meirleir, Anna C Jansen
Pagina's: 420-426 - A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome(2014)
Auteurs: Kim Vancampenhout, Ben Caljon, C Spits, Katrien Stouffs, An Jonckheere, Linda De Meirleir, Willy Lissens, A. Vanlander, Joél Smet, Boel De Paepe, et al.
- Characterization of CoQ₁₀ biosynthesis in fibroblasts of patients with primary and secondary CoQ₁₀ deficiency(2014)
Auteurs: Nuria Buján, Angela Arias, Raquel Montero, Judit García-Villoria, Willy Lissens, Sara Seneca, Carmen Espinós, Plácido Navas, Linda De Meirleir, Rafael Artuch, et al.
Pagina's: 53-62 - DGUOK-related mitochondrial DNA depletion syndrome in a child with an early diagnosis of glycogen storage disease(2013)
Auteurs: Ciğdem S Kasapkara, Leyla Tümer, Aynur Küçükçongar, Alev Hasanoğlu, Sara Seneca, Linda De Meirleir
Pagina's: e28-e29 - Reply to 'Methicillin-resistant Staphylococcus Aureus'(2013)
Auteurs: E. Vanderhelst, Linda De Meirleir, Sylvia Verbanck, Denis Pierard, Walter Vincken, Anne Malfroot
Pagina's: 183-183 - Influence of Botulinum Toxin Therapy on Postural Control and Lower Limb Intersegmental Coordination in Children with Spastic Cerebral Palsy(2013)
Auteurs: M Degelaen, Ludo De Borre, Eric Kerckhofs, Linda De Meirleir, Ronald Buyl, G Cheron, Bernard Dan, Med Florian Lang
Pagina's: 93-105