Show 10 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, LJ*" or (type exact bookEditor and editor="De Meirleir, LJ*") Add to list Conference Paper C3 ACUTE RHABDOMYOLYSIS IN YOUNG CHILDREN DUE TO MUTATIONS IN THE LPIN1 GENE LJ De Meirleir, Patrick Verloo (UGent) , Rudy Van Coster (UGent) , Joél Smet (UGent) , B Wuyts, L Huber and P Delonlay (2009) MOLECULAR GENETICS AND METABOLISM. 98(1-2). Add to list Conference Paper C3 ORGANIC ACIDURIA AND LATE ONSET OPTIC ATROPHY LJ De Meirleir, P Goyens, Patrick Verloo (UGent) , Joél Smet (UGent) , M Vandriessche, K Corthouts, Bart Leroy (UGent) and Rudy Van Coster (UGent) (2009) MOLECULAR GENETICS AND METABOLISM. 98(1-2). Add to list Conference Paper C3 Preliminary screening results for fabry disease in young stroke patients reveals a new mutation Dimitri Hemelsoet (UGent) , Bruce Poppe (UGent) , Anne Sieben (UGent) , FREDERIK VANHEE, PASCAL PROOT, M De Clerck, Bart Leroy (UGent) , Julie De Backer (UGent) , BIRGIT WUYTS (UGent) , LJ De Meirleir, et al. (2007) EUROPEAN JOURNAL OF NEUROLOGY. 14(suppl. 1). p.166-167 Add to list Journal Article A1 Aminoacylase I deficiency: A novel inborn error of metabolism Rudy Van Coster (UGent) , EA GERLO, TG GIARDINA, UF ENGELKE, Joél Smet (UGent) , Claudine De Praeter (UGent) , VALERIE MEERSSCHAUT (UGent) , LJ DE MEIRLEIR, SH SENECA, Bart Devreese (UGent) , et al. (2005) BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 338(3). p.1322-1326