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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Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography–mass spectrometry as a diagnostic test for Barth... von Houtkooper, Riekelt H., Rodenburg, Richard J., Thiels, Charlotte, Lenthe, Henk van, Stet, Femke, Poll-The, Bwee Tien, Stone, Janet E., Steward, Colin G., Wanders, Ronald J., Smeitink, Jan, Kulik, Willem, Vaz, Frédéric M.

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Bloodspot Assay Using HPLC-Tandem Mass Spectrometry for Detection of Barth Syndrome von Kulik, Willem, van Lenthe, Henk, Stet, Femke S, Houtkooper, Riekelt H, Kemp, Helena, Stone, Janet E, Steward, Colin G, Wanders, Ronald J, Vaz, Frederic M

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Clinical Implications of Dihydropyrimidine Dehydrogenase (DPD) Deficiency in Patients with Severe 5-Fluorouracil-associated Toxicity: Identification of New Mutations in the DPD Gen... von VAN KUILENBURG, André B. P, HAASJES, Janet, RICHEL, Dick J, ZOETEKOUW, Lida, VAN LENTHE, Henk, DE ABREU, Ronney A, MARING, Jan G, VREKEN, Peter, VAN GENNIP, Albert H

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Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia von Vaz, Frédéric M, McDermott, John H, Alders, Mariëlle, Wortmann, Saskia B, Kölker, Stefan, Pras-Raves, Mia L, Vervaart, Martin A T, van Lenthe, Henk, Luyf, Angela C M, Elfrink, Hyung L, Metcalfe, Kay, Cuvertino, Sara, Clayton, Peter E, Yarwood, Rebecca, Lowe, Martin P, Lovell, Simon, Rogers, Richard C, van Kampen, Antoine H C, Ruiter, Jos P N, Wanders, Ronald J A, Ferdinandusse, Sacha, van Weeghel, Michel, Engelen, Marc, Banka, Siddharth

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A mutation creating an upstream translation initiation codon in SLC22A5 5′UTR is a frequent cause of primary carnitine deficiency von Ferdinandusse, Sacha, te Brinke, Heleen, Ruiter, Jos P.N., Haasjes, Janet, Oostheim, Wendy, Lenthe, Henk, IJlst, Lodewijk, Ebberink, Merel S., Wanders, Ronald J.A., Vaz, Frédéric M., Waterham, Hans R.

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An improved functional assay in blood spot to diagnose Barth syndrome using the monolysocardiolipin/cardiolipin ratio von Vaz, Frédéric M., Lenthe, Henk, Vervaart, Martin A. T., Stet, Femke S., Klinkspoor, Johanne H., Vernon, Hilary J., Goorden, Susan M. I., Houtkooper, Riekelt H., Kulik, Willem, Wanders, Ronald J. A.

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A sensitive mass spectrometry platform identifies metabolic changes of life history traits in C. elegans von Gao, Arwen W., Chatzispyrou, Iliana A., Kamble, Rashmi, Liu, Yasmine J., Herzog, Katharina, Smith, Reuben L., van Lenthe, Henk, Vervaart, Martin A. T., van Cruchten, Arno, Luyf, Angela C., van Kampen, Antoine, Pras-Raves, Mia L., Vaz, Frédéric M., Houtkooper, Riekelt H.

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A Multiplex Assay for the Diagnosis of Mucopolysaccharidoses and Mucolipidoses von Langereis, Eveline J, Wagemans, Tom, Kulik, Wim, Lefeber, Dirk J, van Lenthe, Henk, Oussoren, Esmee, van der Ploeg, Ans T, Ruijter, George J, Wevers, Ron A, Wijburg, Frits A, van Vlies, Naomi

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Supernatant of stored platelets causes lung inflammation and coagulopathy in a novel in vivo transfusion model von Vlaar, Alexander P.J., Hofstra, Jorrit J., Kulik, Wim, van Lenthe, Henk, Nieuwland, Rienk, Schultz, Marcus J., Levi, Marcel M., Roelofs, Joris J.T.H., Tool, Anton T.J., de Korte, Dirk, Juffermans, Nicole P.

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Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor von Barendsen, Rinse W, Dijkstra, Inge M E, Visser, Wouter F, Alders, Mariëlle, Bliek, Jet, Boelen, Anita, Bouva, Marelle J, van der Crabben, Saskia N, Elsinghorst, Ellen, van Gorp, Ankie G M, Heijboer, Annemieke C, Jansen, Mandy, Jaspers, Yorrick R J, van Lenthe, Henk, Metgod, Ingrid, Mooij, Christiaan F, van der Sluijs, Elise H C, van Trotsenburg, A S Paul, Verschoof-Puite, Rendelien K, Vaz, Frédéric M, Waterham, Hans R, Wijburg, Frits A, Engelen, Marc, Dekkers, Eugènie, Kemp, Stephan

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Comparison of the Diagnostic Performance of C26:0-Lysophosphatidylcholine and Very Long-Chain Fatty Acids Analysis for Peroxisomal Disorders von Jaspers, Yorrick R J, Ferdinandusse, Sacha, Dijkstra, Inge M E, Barendsen, Rinse Willem, van Lenthe, Henk, Kulik, Wim, Engelen, Marc, Goorden, Susan M I, Vaz, Frédéric M, Kemp, Stephan

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Gallstone Formation Follows a Different Trajectory in Bariatric Patients Compared to Nonbariatric Patients von Haal, Sylke, Guman, Maimoena S S, Acherman, Yair I Z, Jansen, Johannes P G, van Weeghel, Michel, van Lenthe, Henk, Wever, Eric J M, Gerdes, Victor E A, Voermans, Rogier P, Groen, Albert K

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Identification and characterization of human cardiolipin synthase von Houtkooper, Riekelt H., Akbari, Hana, van Lenthe, Henk, Kulik, Willem, Wanders, Ronald J.A., Frentzen, Margrit, Vaz, Frédéric M.

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Corrigendum: Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor von Barendsen, Rinse W, Dijkstra, Inge M E, Visser, Wouter F, Alders, Mariëlle, Bliek, Jet, Boelen, Anita, Bouva, Marelle J, van der Crabben, Saskia N, Elsinghorst, Ellen, van Gorp, Ankie G M, Heijboer, Annemieke C, Jansen, Mandy, Jaspers, Yorrick R J, van Lenthe, Henk, Metgod, Ingrid, Mooij, Christiaan F, van der Sluijs, Elise H C, van Trotsenburg, A S Paul, Verschoof-Puite, Rendelien K, Vaz, Frédéric M, Waterham, Hans R, Wijburg, Frits A, Engelen, Marc, Dekkers, Eugènie, Kemp, Stephan

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New insights in dihydropyrimidine dehydrogenase deficiency: a pivotal role for beta-aminoisobutyric acid? von Van Kuilenburg, André B P, Stroomer, Alida E M, Van Lenthe, Henk, Abeling, Nico G G M, Van Gennip, Albert H

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Tracer‐based lipidomics enables the discovery of disease‐specific candidate biomarkers in mitochondrial β‐oxidation disorders von Schwantje, Marit, Mosegaard, Signe, Knottnerus, Suzan J. G., Klinken, Jan Bert, Wanders, Ronald J., Lenthe, Henk, Hermans, Jill, IJlst, Lodewijk, Denis, Simone W., Jaspers, Yorrick R. J., Fuchs, Sabine A., Houtkooper, Riekelt H., Ferdinandusse, Sacha, Vaz, Frédéric M.

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Tracer-based lipidomics enables the discovery of disease-specific candidate biomarkers in mitochondrial β-oxidation disorders von Schwantje, Marit, Mosegaard, Signe, Knottnerus, Suzan J G, van Klinken, Jan Bert, Wanders, Ronald J, van Lenthe, Henk, Hermans, Jill, IJlst, Lodewijk, Denis, Simone W, Jaspers, Yorrick R J, Fuchs, Sabine A, Houtkooper, Riekelt H, Ferdinandusse, Sacha, Vaz, Frédéric M

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HPLC-Electrospray Tandem Mass Spectrometry for Rapid Determination of Dihydropyrimidine Dehydrogenase Activity von van Kuilenburg, Andre B.P, van Lenthe, Henk, Zoetekouw, Lida, Kulik, Willem

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Defects in Pyrimidine Degradation Identified by HPLC-Electrospray Tandem Mass Spectrometry of Urine Specimens or Urine-soaked Filter Paper Strips von van Lenthe, Henk, van Kuilenburg, Andre B.P, Ito, Tetsuya, Bootsma, Albert H, van Cruchten, Arno, Wada, Yoshiro, van Gennip, Albert H

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