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
1 - 10 van 63
- Parenteral hydroxocobalamin dose intensification in five patients with different types of early onset intracellular cobalamin defects(2019)
Auteurs: Emmanuel Scalais, Elise Osterheld, Christine Geron, Charlotte Pierron, Ronit Chafai, Vincent Schlesser, Patricia Borde, Luc Régal, Hilde Laeremans, Koen L I van Gassen, et al.
Pagina's: 70-79 - Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial(2019)
Auteurs: Stefan Groeneweg, Robin P. Peeters, Carla Moran, Mb Athanasia Stoupa, Francoise Auriol, Davide Tonduti, Alice Dica, Laura Paone, Klara Rozenkova, Jana Malikova, et al.
Pagina's: 695-706 - Research activity and capability in the European reference network MetabERN(2019)
Auteurs: Jean-Michel Heard, Cinzia Bellettato, Corine van Lingen, Francois-Guillaume Debray, Marie-Cecile Nassogne, Rudy Van Coster, Linda De Meirleir, Francois Eyskens, Eva Morava, Ivo Baric, et al.
Pagina's: 119 - Multidisciplinary diagnostic settings for children with a neurobiological developmental delay or disorder in Flanders: comparison of governmental regulations.(2019)Edition: S2Volume: 61
Auteurs: Linda De Meirleir
Pagina's: 7-7Aantal pagina's: 1 - Clinical implementation of gene panel testing for lysosomal storage diseases(2019)
Auteurs: Alexander Gheldof, Sara Seneca, Katrien Stouffs, Willy Lissens, Anna C Jansen, Hilde Laeremans, Patrick Verloo, An-Sofie Schoonjans, Marije Meuwissen, Diana Barca, et al.
- Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases(2019)
Auteurs: Roland Posset, Sven F. Garbade, S P Nikolas Boy, Alberto B Burlina, Carlo Dionisi-Vici, Dries Dobbelaere, Angeles Garcia-Cazorla, Pascale De Lonlay, Elisa Leao Teles, Roshni Vara, et al.
Pagina's: 93-106 - Efficacy and safety of Velmanase alfa in the treatment of patients with alpha-mannosidosis(2018)
Auteurs: Line Borgwardt, Nathalie Guffon, Yasmina Amraoui, Christine I. Dali, Linda De Meirleir, Mercedes Gil Campos, Bénédicte Heron, Silvia Geraci, Diego Ardigò, Federica Cattaneo, et al.
Pagina's: 1215-1223 - Comprehensive long-term efficacy and safety of recombinant human alpha-mannosidase (velmanase alfa) treatment in patients with alpha-mannosidosis(2018)
Auteurs: Allan Meldgaard Lund, Line Borgwardt, Federica Cattaneo, Diego Ardigò, Silvia Geraci, Mercedes Gil Campos, Linda De Meirleir, Cécile Laroche, Philippe Dolhem, Duncan Cole, et al.
Pagina's: 1225-1233 - International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome(2018)
Auteurs: Rossella Parini, Alexander Broomfield, Maureen Anne Cleary, Linda De Meirleir, Maja Di Rocco, Waseem Mahmoud Fathalla, Nathalie Guffon, Christina Lampe, Allan Meldgaard Lund, Maurizio Scarpa, et al.
Pagina's: 2059-2065 - Easy-to-use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment(2018)
Auteurs: Anna Tylki-Szymańska, Linda De Meirleir, Maja Di Rocco, Waseem M Fathalla, Nathalie Guffon, Christina Lampe, Allan Meldgaard Lund, Rossella Parini, Frits A Wijburg, Jiri Zeman, et al.
Pagina's: 1402-1408