Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: A review von Silva, M. F. B., Aires, C. C. P., Luis, P. B. M., Ruiter, J. P. N., IJlst, L., Duran, M., Wanders, R. J. A., Tavares de Almeida, I.

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Phytanic acid: production from phytol, its breakdown and role in human disease von van den Brink, D M, Wanders, R J A

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Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy von Gobin-Limballe, S., Djouadi, F., Aubey, F., Olpin, S., Andresen, B.S., Yamaguchi, S., Mandel, H., Fukao, T., Ruiter, J.P.N., Wanders, R.J.A., McAndrew, R., Kim, J.J., Bastin, J.

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Clinical variability of isovaleric acidemia in a genetically homogeneous population von Dercksen, M., Duran, M., IJlst, L., Mienie, L. J., Reinecke, C. J., Ruiter, J. P. N., Waterham, H. R., Wanders, R. J. A.

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Pyruvate dehydrogenase kinase 4 expression is synergistically induced by AMP-activated protein kinase and fatty acids von Houten, S. M, Chegary, M, te Brinke, H, Wijnen, W. J, Glatz, J. F. C, Luiken, J. J. F. P, Wijburg, F. A, Wanders, R. J. A

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Fatty acid metabolism in Saccharomyces cerevisiae von van Roermund, C W T, Waterham, H R, Ijlst, L, Wanders, R J A

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Phytanic acid impairs mitochondrial respiration through protonophoric action von Komen, J. C, Distelmaier, F, Koopman, W. J. H, Wanders, R. J. A, Smeitink, J, Willems, P. H. M. G

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Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency von Derks, T. G. J., Boer, T. S., van Assen, A., Bos, T., Ruiter, J., Waterham, H. R., Niezen-Koning, K. E., Wanders, R. J. A., Rondeel, J. M. M., Loeber, J. G., ten Kate, L. P., Smit, G. P. A., Reijngoud, D.-J.

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Polyunsaturated fatty acid status in treated isovaleric acidemia patients von Dercksen, M, Kulik, W, Mienie, L J, Reinecke, C J, Wanders, R J A, Duran, M

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The Inflammatory Response in Acyl-CoA Oxidase 1 Deficiency (Pseudoneonatal Adrenoleukodystrophy) von El Hajj, H. I, Vluggens, A, Andreoletti, P, Ragot, K, Mandard, S, Kersten, S, Waterham, H. R, Lizard, G, Wanders, R. J. A, Reddy, J. K, Cherkaoui-Malki, Mustapha

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Mutations in the Gene Encoding Peroxisomal Sterol Carrier Protein X (SCPx) Cause Leukencephalopathy with Dystonia and Motor Neuropathy von Ferdinandusse, S., Kostopoulos, P., Denis, S., Rusch, H., Overmars, H., Dillmann, U., Reith, W., Haas, D., Wanders, R.J.A., Duran, M., Marziniak, M.

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Rhabdomyolysis: Review of the literature von Zutt, R, van der Kooi, A.J, Linthorst, G.E, Wanders, R.J.A, de Visser, M

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MRI as diagnostic tool in early-onset peroxisomal disorders von VAN DER KNAAP, M. S, WASSMER, E, WOLF, N. I, FERREIRA, P, TOPCU, M, WANDERS, R. J. A, WATERHAM, H. R, FERDINANDUSSE, S

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RELAPSING RHABDOMYOLYSIS DUE TO PEROXISOMAL α-METHYLACYL-COA RACEMASE DEFICIENCY von KAPINA, V, SEDEL, F, TRUFFERT, A, HORVATH, J, WANDERS, R. J. A, WATERHAM, H. R, PICARD, F

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Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress von Spiekerkoetter, U., Tokunaga, C., Wendel, U., Mayatepek, E., Exil, V., Duran, M., Wijburg, F. A., Wanders, R. J. A., Strauss, A. W.

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High activity of fatty acid oxidation enzymes in human placenta: Implications for fetal‐maternal disease von Oey, N. A., Den Boer, M. E. J., Ruiter, J. P. N., Wanders, R. J. A., Duran, M., Waterham, H. R., Boer, K., der Post, J. A. M., Wijburg, F. A.

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Peroxisomes, lipid metabolism and lipotoxicity von Wanders, R.J.A., Ferdinandusse, S., Brites, P., Kemp, S.

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Identification and Characterization of Three Novel Missense Mutations in Mevalonate Kinase cDNA Causing Mevalonic Aciduria, a Disorder of Isoprene Biosynthesis von Houten, S. M., Romeijn, G. J., Koster, J., Gray, R. G. F., Darbyshire, P., Smit, G. P. A., de Klerk, J. B. C., Duran, M., Gibson, K. M., Wanders, R. J. A., Waterham, H. R.

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Relapsing encephalopathy in a patient with α-methylacyl-CoA racemase deficiency von Thompson, S A, Calvin, J, Hogg, S, Ferdinandusse, S, Wanders, R J A, Barker, R A

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Catecholamine excretion profiles identify clinical subgroups of neuroblastoma patients von Verly, I.R.N., Leen, R., Meinsma, J.R., Hooijer, G.K.J., Savci-Heijink, C.D., van Nes, J., Broekmans, M., Wanders, R.J.A., van Kuilenburg, A.B.P., Tytgat, G.A.M.

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