Fatty acid omega-oxidation as a rescue pathway for fatty acid oxidation disorders in humans von Wanders, Ronald J.A, Komen, Jasper, Kemp, Stephan

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X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management von Engelen, Marc, Kemp, Stephan, de Visser, Marianne, van Geel, Björn M, Wanders, Ronald J A, Aubourg, Patrick, Poll-The, Bwee Tien

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The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives von Bosch, Annet M, Stroek, Kevin, Abeling, Nico G, Waterham, Hans R, Ijlst, Lodewijk, Wanders, Ronald J A

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Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism von Pougovkina, Olga, te Brinke, Heleen, Wanders, Ronald J. A., Houten, Sander M., de Boer, Vincent C. J.

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enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results von Wanders, Ronald J. A, Ruiter, Jos P. N, IJlst, Lodewijk, Waterham, Hans R, Houten, Sander M

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C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man von van de Beek, Malu-Clair, Dijkstra, Inge M E, van Lenthe, Henk, Ofman, Rob, Goldhaber-Pasillas, Dalia, Schauer, Nicolas, Schackmann, Martin, Engelen-Lee, Joo-Yeon, Vaz, Frédéric M, Kulik, Wim, Wanders, Ronald J A, Engelen, Marc, Kemp, Stephan

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Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy von Gragnaniello, Vincenza, Gueraldi, Daniela, Puma, Andrea, Commone, Anna, Cazzorla, Chiara, Loro, Christian, Porcù, Elena, Stornaiuolo, Maria, Miglioranza, Paolo, Salviati, Leonardo, Wanders, Ronald J. A, Burlina, Alberto

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Impaired Bile Acid Homeostasis in Children with Severe Acute Malnutrition von Zhang, Ling, Voskuijl, Wieger, Mouzaki, Marialena, Groen, Albert K, Alexander, Jennifer, Bourdon, Celine, Wang, Alice, Versloot, Christian J, Di Giovanni, Valeria, Wanders, Ronald J A, Bandsma, Robert

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Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway von Wanders, Ronald J. A., Duran, Marinus, Loupatty, Ference J.

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The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders von Houten, Sander M, Violante, Sara, Ventura, Fatima V, Wanders, Ronald J.A

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The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders von Ferdinandusse, Sacha, Ebberink, Merel S., Vaz, Frédéric M., Waterham, Hans R., Wanders, Ronald J. A.

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The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters von Roermund, Carlo W. T., Visser, Wouter F., IJlst, Lodewijk, Cruchten, Arno, Boek, Maxim, Kulik, Wim, Waterham, Hans R., Wanders, Ronald J. A.

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Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient mice von Brites, Pedro, Ferreira, Ana Sofia, da Silva, Tiago Ferreira, Sousa, Vera F, Malheiro, Ana R, Duran, Marinus, Waterham, Hans R, Baes, Myriam, Wanders, Ronald J A

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Mice with a deficiency in Peroxisomal Membrane Protein 4 (PXMP4) display mild changes in hepatic lipid metabolism von Blankestijn, Maaike, Bloks, Vincent W., Struik, Dicky, Huijkman, Nicolette, Kloosterhuis, Niels, Wolters, Justina C., Wanders, Ronald J. A., Vaz, Frédéric M., Islinger, Markus, Kuipers, Folkert, van de Sluis, Bart, Groen, Albert K., Verkade, Henkjan J., Jonker, Johan W.

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Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acids von De Marcos Lousa, Carine, van Roermund, Carlo W. T., Postis, Vincent L. G., Dietrich, Daniela, Kerr, Ian D., Wanders, Ronald J. A., Baldwin, Stephen A., Baker, Alison, Theodoulou, Frederica L.

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Monocarboxylate Transporter 1 Deficiency and Ketone Utilization von van Hasselt, Peter M, Ferdinandusse, Sacha, Monroe, Glen R, Ruiter, Jos P.N, Turkenburg, Marjolein, Geerlings, Maartje J, Duran, Karen, Harakalova, Magdalena, van der Zwaag, Bert, Monavari, Ardeshir A, Okur, Ilyas, Sharrard, Mark J, Cleary, Maureen, O’Connell, Nuala, Walker, Valerie, Rubio-Gozalbo, M. Estela, de Vries, Maaike C, Visser, Gepke, Houwen, Roderick H.J, van der Smagt, Jasper J, Verhoeven-Duif, Nanda M, Wanders, Ronald J.A, van Haaften, Gijs

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Peroxisomal D-bifunctional protein deficiency: Three adults diagnosed by whole-exome sequencing von Lines, Matthew A, Jobling, Rebekah, Brady, Lauren, Marshall, Christian R, Scherer, Stephen W, Rodriguez, Amadeo R, Lee, Liesly, Lang, Anthony E, Mestre, Tiago A, Wanders, Ronald J.A, Ferdinandusse, Sacha, Tarnopolsky, Mark A

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general introduction to the biochemistry of mitochondrial fatty acid β-oxidation von Houten, Sander Michel, Wanders, Ronald J. A

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Mammalian peroxisomal ABC transporters: from endogenous substrates to pathology and clinical significance von Kemp, Stephan, Theodoulou, Frederica L, Wanders, Ronald JA

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NAD+ homeostasis in human health and disease von Zapata‐Pérez, Rubén, Wanders, Ronald J A, van Karnebeek, Clara D M, Houtkooper, Riekelt H

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