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Molecular Genetics and Metabolism|July 14, 2006
Bezafibrate induces FALDH in human fibroblasts; implications for Sjögren-Larsson syndromeJ Gloerich, L Ijlst, R J A Wanders, et al.Biochimica Et Biophysica Acta|January 13, 2010
Peroxisomes, lipid metabolism and lipotoxicityR J A Wanders, S Ferdinandusse, P Brites, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 28, 2002
A new defect of peroxisomal function involving pristanic acid: a case reportB N McLean, J Allen, S Ferdinandusse, et al.Neurology|June 9, 2004
Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorderJ Gootjes, F Skovby, E Christensen, et al.Journal of Lipid Research|March 8, 2000
Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed methodS Ferdinandusse, S Denis, E van Berkel, et al.JIMD Reports|September 26, 2015
Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyP Bala, S Ferdinandusse, S E Olpin, et al.Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.Journal of Lipid Research|February 13, 2001
Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiencyS Ferdinandusse, H Overmars, S Denis, et al.Biochemical and Biophysical Research Communications|September 16, 1999
Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acidsS Ferdinandusse, J Mulders, L IJlst, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 23, 2007
Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiencyS A Thompson, J Calvin, S Hogg, et al.Pageof 3