Show 5 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="DE MEIRLEIR, L" or (type exact bookEditor and editor="DE MEIRLEIR, L") Add to list Journal Article A1 open access Clinical implementation of gene panel testing for lysosomal storage diseases A Gheldof, S Seneca, K Stouffs, W Lissens, A Jansen, H Laeremans, Patrick Verloo (UGent) , AS Schoonjans, M Meuwissen, D Barca, et al. (2019) MOLECULAR GENETICS & GENOMIC MEDICINE. 7(2). Add to list Conference Paper C3 Database crossing allows better understanding of neuromuscular disorders epidemiology: the Belgian example C Bleyenheuft, P Van Damme, N Goemans, Jan De Bleecker (UGent) , Rudy Van Coster (UGent) , P De Jonghe, D Beysen, P Van den Bergh, F Christiaens, A Maertens de Noordhout, et al. (2016) NEUROMUSCULAR DISORDERS. 26(suppl. 2). p.S207-S207 Add to list Journal Article A1 open access Multiple phenotypes in phosphoglucomutase 1 deficiency LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, K Raymond, P He, M Ichikawa, J Veltman, et al. (2014) NEW ENGLAND JOURNAL OF MEDICINE. 370(6). p.533-542 Add to list Journal Article A1 TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria AC Jansen, Ann Oostra (UGent) , B Desprechins, Y De Vlaeminck, Helene Verhelst (UGent) , L Regal, Patrick Verloo (UGent) , N Bockaert, K Keymolen, S Seneca, et al. (2011) NEUROLOGY. 76(11). p.988-992 Add to list Journal Article A1 Mutations in SACS cause atypical and late-onset forms of ARSACS J Baets, T Deconinck, K Smets, D Goossens, P Van Den Bergh, K Dahan, E Schmedding, Patrick Santens (UGent) , Milic V Rasic, P Van Damme, et al. (2010) NEUROLOGY. 75(13). p.1181-1188 1 2 3 4 … 10 11 Next →