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

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Medical nutrition therapy in patients with HIBCH and ECHS1 defects: Clinical and biochemical response to low valine diet von Abdenur, J.E., Sowa, M., Simon, M., Steenari, M., Skaar, J., Eftekharian, S., Chang, R., Ferdinandusse, S., Pitt, J.

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Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene von Ebberink, Merel S, Csanyi, Barbara, Chong, Wui K, Denis, Simone, Sharp, Peter, Mooijer, Petra A W, Dekker, Conny J M, Spooner, Claire, Ngu, Lock H, De Sousa, Carlos, Wanders, Ronald J A, Fietz, Michael J, Clayton, Peter T, Waterham, Hans R, Ferdinandusse, Sacha

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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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Diagnostic pitfall in antenatal manifestations of CPT II deficiency von Boemer, F., Deberg, M., Schoos, R., Caberg, J.-H., Gaillez, S., Dugauquier, C., Delbecque, K., François, A., Maton, P., Demonceau, N., Senterre, G., Ferdinandusse, S., Debray, F.-G.

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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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Subcellular localization and physiological role of alpha-methylacyl-CoA racemase von Ferdinandusse, S, Denis, S, IJlst, L, Dacremont, G, Waterham, H R, Wanders, R J

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A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways von Gloerich, J., van Vlies, N., Jansen, G.A., Denis, S., Ruiter, J.P.N., van Werkhoven, M.A., Duran, M., Vaz, F.M., Wanders, R.J.A., Ferdinandusse, S.

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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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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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Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene von Jansen, Gerbert A, Oftnan, Rob, Ferdinandusse, Sacha, Ijlst, Lodewijk, Muijsers, Anton O, Skjeldal, Ola H, Stokke, Oddvar, Jakobs, Cornells, Besley, Guy T.N, Wraith, J. Ed, Wanders, Ronald J.A

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520P Periodic paralysis in a child with thermosensitive mitochondrial trifunctional protein deficiency von Al-Amrani, F., Ruiter, J., Doolaard, M., Kumar, A., Ferdinandusse, S., Al-Thihli, K.

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Bezafibrate induces FALDH in human fibroblasts; implications for Sjögren-Larsson syndrome von Gloerich, J., IJlst, L., Wanders, R.J.A., Ferdinandusse, S.

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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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Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders von Ferdinandusse, S, Rusch, H, van Lint, A E M, Dacremont, G, Wanders, R J A, Vreken, P

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Tremor and deep white matter changes in α-methylacyl-CoA racemase deficiency von CLARKE, C. E, ALGER, S, PREECE, M. A, BURDON, M. A, CHAVDA, S, DENIS, S, FERDINANDUSSE, S, WANDERS, R. J. A

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Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder von Maxit, C., Denzler, I., Marchione, D., Agosta, G., Koster, J., Wanders, R. J. A., Ferdinandusse, S., Waterham, H. R.

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Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder von GOOTJES, J, SKOVBY, F, CHRISTENSEN, E, WANDERS, R. J. A, FERDINANDUSSE, S

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Autosomal dominant Zellweger Spectrum Disorder caused by de novo variants in PEX14 gene von Waterham, Hans R., Koster, Janet, Ebberink, Merel S., Jesina, Pavel, Zeman, Jiri, Noskova, Lenka, Kmoch, Stanislav, Devic, Perrine, Cheillan, David, Wanders, Ronald J.A., Ferdinandusse, Sacha

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Pitfall in Metabolic Screening in a Patient with Fatal Peroxisomal β-Oxidation Defect von Rosewich, H., Waterham, H. R., Wanders, R. J. A., Ferdinandusse, S., Henneke, M., Hunneman, D., Gärtner, J.

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