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Tijdschrift Voor Kindergeneeskunde|December 1, 1984
[Diagnosis of Zellweger's cerebrohepatorenal syndrome]R B Schutgens, H S Heymans, R Purvis, et al.Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Clinical and Laboratory Diagnosis of Peroxisomal DisordersRonald J A Wanders, Femke C C Klouwer, Sacha Ferdinandusse, et al.Pflugers Archiv : European Journal of Physiology|October 14, 2006
The peroxisomal ABC transporter familyRonald J A Wanders, Wouter F Visser, Carlo W T van Roermund, et al.Biochemical and Biophysical Research Communications|April 10, 2007
Demonstration of bile acid transport across the mammalian peroxisomal membraneWouter F Visser, Carlo W T van Roermund, Lodewijk Ijlst, et al.Molecular Genetics and Metabolism|February 20, 2004
Human mevalonate pyrophosphate decarboxylase is localized in the cytosolSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2010
Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophySacha Ferdinandusse, Simon Barker, Katherine Lachlan, et al.BMC Cancer|October 21, 2011
Cancer associated epigenetic transitions identified by genome-wide histone methylation binding profiles in human colorectal cancer samples and paired normal mucosaStefan Enroth, Alvaro Rada-Iglesisas, Robin Andersson, et al.Biochimie|January 1, 1993
Ether lipid synthesis and its deficiency in peroxisomal disordersH van den Bosch, G Schrakamp, D Hardeman, et al.Annals of the New York Academy of Sciences|December 27, 1996
Metabolic aspects of peroxisomal disordersR J Wanders, G Jansen, C W van Roermund, et al.Obesity (Silver Spring, Md.)|June 18, 2019
Dietary Methionine Restriction Reduces Inflammation Independent of FGF21 ActionShaligram Sharma, Taylor Dixon, Sean Jung, et al.Pageof 132