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Kidney International|July 16, 2004
Clinical implications of mutation analysis in primary hyperoxaluria type 1Christiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.The Biochemical Journal|February 25, 2005
Demonstration and characterization of phosphate transport in mammalian peroxisomesWouter F Visser, Carlo W Van Roermund, Lodewijk Ijlst, et al.International Journal of Methods in Psychiatric Research|July 3, 2019
Practical consequences of model misfit when using rating scales to assess the severity of attention problems in childrenDaniela R Crișan, Jorge N Tendeiro, Rob B K Wanders, et al.JIMD Reports|August 26, 2016
Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum DisorderC Maxit, I Denzler, D Marchione, et al.Molecular Microbiology|December 4, 2003
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndromeZhiming Gu, Fredoen Valianpour, Shuliang Chen, et al.Journal of Inherited Metabolic Disease|January 1, 1989
Deficient oxidation of trihydroxycoprostanic acid in liver homogenates from patients with peroxisomal diseasesM Casteels, C W Van Roermund, L Schepers, et al.Annals of Neurology|July 12, 2002
Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiencyRegina Ensenauer, Helmut Niederhoff, Jos P N Ruiter, et al.Circulation Research|January 29, 2019
Associations of Monounsaturated Fatty Acids From Plant and Animal Sources With Total and Cause-Specific Mortality in Two US Prospective Cohort StudiesMarta Guasch-Ferré, Geng Zong, Walter C Willett, et al.Journal of the Neurological Sciences|December 1, 1988
Peroxisomal disorders in neurologyR J Wanders, H S Heymans, R B Schutgens, et al.Journal of Inherited Metabolic Disease|April 8, 2006
Fatty acid oxidation in the human fetus: implications for fetal and adult diseaseNadia A Oey, Jos P N Ruiter, Tania Attié-Bitach, et al.Pageof 132