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Journal of the Neurological Sciences|August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case reportR J Wanders, E Boltshauser, B Steinmann, et al.
Kidney International|November 1, 1996
Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluriaK J Van Acker, F J Eyskens, M F Espeel, et al.
Molecular Genetics and Metabolism|September 2, 2003
Evidence for increased oxidative stress in peroxisomal D-bifunctional protein deficiencySacha Ferdinandusse, Barbara Finckh, Yvette C de Hingh, et al.
The Journal of Biological Chemistry|May 15, 1993
The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidneyG F Vanhove, P P Van Veldhoven, M Fransen, et al.
BMJ (Clinical Research Ed.)|November 25, 2016
Intake of individual saturated fatty acids and risk of coronary heart disease in US men and women: two prospective longitudinal cohort studiesGeng Zong, Yanping Li, Anne J Wanders, et al.
Biochemical Pharmacology|February 14, 1995
Meta-iodobenzylguanidine inhibits complex I and III of the respiratory chain in the human cell line Molt-4J Cornelissen, R J Wanders, A H Van Gennip, et al.
European Journal of Cancer (Oxford, England : 1990)|March 15, 2005
Phase I study and pharmacokinetic of CHS-828, a guanidino-containing compound, administered orally as a single dose every 3 weeks in solid tumours: an ECSG/EORTC studyAlain Ravaud, Thomas Cerny, Catherine Terret, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Molecular Genetics and Metabolism|September 17, 2005
Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiencyAndrás N Spaan, Lodewijk Ijlst, Carlo W T van Roermund, et al.
The Journal of Clinical Investigation|March 1, 1993
Impaired degradation of leukotrienes in patients with peroxisome deficiency disordersE Mayatepek, W D Lehmann, J Fauler, et al.
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