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Journal of Inherited Metabolic Disease|November 7, 2008
The biochemistry, metabolism and inherited defects of the pentose phosphate pathway: a reviewM M C Wamelink, E A Struys, C JakobsActa Clinica Belgica|April 4, 2014
Pyroglutamic acid-induced metabolic acidosis: a case reportS Luyasu, M M C Wamelink, L Galanti, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Analysis of polyols in urine by liquid chromatography-tandem mass spectrometry: a useful tool for recognition of inborn errors affecting polyol metabolismM M C Wamelink, D E C Smith, C Jakobs, et al.Molecular Genetics and Metabolism|October 23, 2010
4-Hydroxybutyric aciduria associated with catheter usage: a diagnostic pitfall in the identification of SSADH deficiencyM M C Wamelink, B Roos, E E W Jansen, et al.Molecular Genetics and Metabolism|January 4, 2011
Elevated concentrations of sedoheptulose in bloodspots of patients with cystinosis caused by the 57-kb deletion: implications for diagnostics and neonatal screeningM M C Wamelink, E A Struys, E E W Jansen, et al.Neuropediatrics|May 6, 2011
N-acetylaspartylglutamate in CNS hypomyelinationM M C Wamelink, E Struys, U Holwerda, et al.Journal of Medical Genetics|May 7, 2013
Phenotype and genotype in 101 males with X-linked creatine transporter deficiencyJ M van de Kamp, O T Betsalel, S Mercimek-Mahmutoglu, et al.Pageof 1