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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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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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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2‐Methyl‐3‐hydroxybutyryl‐CoA dehydrogenase deficiency in a 23‐year‐old man von Olpin, S. E., Pollitt, R. J., McMenamin, J., Manning, N. J., Besley, G., Ruiter, J. P. N., Wanders, R. J. A.

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Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy von INNES, A. M, SEARGEANT, L. E, BALACHANDRA, K, ROE, C. R, WANDERS, R. J. A, RUITER, J. P. N, CASIRO, O, GREWAR, D. A, GREENBERG, C. R

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Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders von Djouadi, F., Aubey, F., Schlemmer, D., Ruiter, J.P.N., Wanders, R.J.A., Strauss, A.W., Bastin, Jean

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Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy von Westermann, C.M, Dorland, L, Votion, D.M, de Sain-van der Velden, M.G.M, Wijnberg, I.D, Wanders, R.J.A, Spliet, W.G.M, Testerink, N, Berger, R, Ruiter, J.P.N, van der Kolk, J.H

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Carnitine supplementation induces long‐chain acylcarnitine production—Studies in the VLCAD‐deficient mouse von Liebig, M., Gyenes, M., Brauers, G., Ruiter, J. P. N., Wendel, U., Mayatepek, E., Strauss, A. W., Wanders, R. J. A., Spiekerkoetter, U.

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Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain von Oey, N.A., Ruiter, J.P.N., IJlst, L., Attie-Bitach, T., Vekemans, M., Wanders, R.J.A., Wijburg, F.A.

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Thermo‐sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy von Schwantje, Marit, Ebberink, Merel S., Doolaard, Mirjam, Ruiter, Jos P. N., Fuchs, Sabine A., Darin, Niklas, Hedberg‐Oldfors, Carola, Régal, Luc, Donker Kaat, Laura, Huidekoper, Hidde H., Olpin, Simon, Cole, Duncan, Moat, Stuart J., Visser, Gepke, Ferdinandusse, Sacha

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Succinyl-CoA :acetoacetate transferase deficiency : identification of a new patient with a neonatal onset and review of the literature von NIEZEN-KONING, K. E, WANDERS, R. J. A, RUITER, J. P. N, IJLST, L, VISSER, G, REITSMA-BIERENS, W. C. C, HEYMANS, H. S. A, REIJNGOUD, D. J, SMIT, G. P. A

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Metabolism of phytol to phytanic acid in the mouse, and the role of PPARα in its regulation von Gloerich, J., van den Brink, D.M., Ruiter, J. P.N., van Vlies, N., Vaz, F.M., Wanders, R. J.A., Ferdinandusse, S.

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Lactic acidosis in long‐chain fatty acid β‐oxidation disorders von Ventura, F. V., Ruiter, J. P. N., IJlst, L., Tavares de Almeida, I., Wanders, R. J. A.

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A new case of succinyl‐CoA:acetoacetate transferase deficiency: Favourable course despite very low residual activity von Barić, I., Sarnavka, V., Fumić, K., Maradin, M., Begović, D., Ruiter, J. P. N., Wanders, R. J. A.

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Valproate inhibits the mitochondrial pyruvate‐driven oxidative phosphorylation in vitro von Silva, M. F. B., Ruiter, J. P. N., IJlst, L., Jakobs, C., Duran, M., Almeida, I. Tavares, Wanders, R. J. A.

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Peroxisomal trans-2-enoyl-CoA reductase is involved in phytol degradation von Gloerich, J., Ruiter, J.P.N., van den Brink, D.M., Ofman, R., Ferdinandusse, S., Wanders, R.J.A.

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Inhibitory effect of 3‐hydroxyacyl‐CoAs and other long‐chain fatty acidβ‐oxidation intermediates on mitochondrial oxidative phosphorylation von Ventura, F. V., Ruiter, J. P. N., Ijlst, L., Tavares de Almeida, I., Wanders, R. J. A.

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Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype von Ijlst, L., Uskikubo, S., Kamijo, T., Hashimoto, T., Ruiter, J. P. N., Klerk, J. B. C., Wanders, R. J. A.

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Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP‐synthesis in digitonin‐permeabilized cells von Wanders, R. J. A., Ruiter, J. P. N., Wijburg, F. A., Zeman, J., Klement, P., Houstek, J.

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