Update of the Pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants. 29/05/2013 Lees meer
Characteristics of early MRI in children and adolescents with vanishing white matter. 19/03/2013 Lees meer
Autumn meeting of the Belgian Society of Pediatric Neurology:‘Spinal cord and plexus’ 19/10/2012 Lees meer
Methylation defect in imprinted genes detected in patients with an Albright’s hereditary osteodystrophy like phenotype and platelet Gs hypofunction. 05/06/2012 Lees meer
