R. A. Wevers

Oligosaccharide excretion in adult Gaucher disease

R. Wevers, C. Hollak, S. van Weely, 1998, Journal of Inherited Metabolic Disease.

Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder

R. Wevers, J. Jaeken, R. Steet, 2005, Journal of Inherited Metabolic Disease.

Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidine

L. Vissers, U. Engelke, K. Coene, 2019, Journal of inherited metabolic disease.