Development and validation of a gas chromatography–mass spectrometry method to analyze octanoate enrichments at low concentrations in human plasma by van Harskamp, Dewi, Knottnerus, Suzan J. G., Visser, Gepke, van Goudoever, Johannes B., Schierbeek, Henk

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Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle by Knottnerus, Suzan J. G., Bleeker, Jeannette C., Wüst, Rob C. I., Ferdinandusse, Sacha, IJlst, Lodewijk, Wijburg, Frits A., Wanders, Ronald J. A., Visser, Gepke, Houtkooper, Riekelt H.

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Tracer‐based lipidomics enables the discovery of disease‐specific candidate biomarkers in mitochondrial β‐oxidation disorders by 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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Prediction of phenotypic severity in mucopolysaccharidosis type IIIA by Knottnerus, Suzan J. G., Nijmeijer, Stephanie C. M., IJlst, Lodewijk, te Brinke, Heleen, van Vlies, Naomi, Wijburg, Frits A.

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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates by Knottnerus, Suzan J G, Mengarelli, Isabella, Wüst, Rob C I, Baartscheer, Antonius, Bleeker, Jeannette C, Coronel, Ruben, Ferdinandusse, Sacha, Guan, Kaomei, IJlst, Lodewijk, Li, Wener, Luo, Xiaojing, Portero, Vincent M, Ulbricht, Ying, Visser, Gepke, Wanders, Ronald J A, Wijburg, Frits A, Verkerk, Arie O, Houtkooper, Riekelt H, Bezzina, Connie R

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Exploring the metabolic fate of medium-chain triglycerides in healthy individuals using a stable isotope tracer by Knottnerus, Suzan J.G., van Harskamp, Dewi, Schierbeek, Henk, Bleeker, Jeannette C., Crefcoeur, Loek L., Ferdinandusse, Sacha, van Goudoever, Johannes B., Houtkooper, Riekelt H., IJlst, Lodewijk, Langeveld, Mirjam, Wanders, Ronald J.A., Vaz, Frédéric M., Wijburg, Frits A., Visser, Gepke

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Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots by Knottnerus, Suzan J.G., Pras-Raves, Mia L., van der Ham, Maria, Ferdinandusse, Sacha, Houtkooper, Riekelt H., Schielen, Peter C.J.I., Visser, Gepke, Wijburg, Frits A., de Sain-van der Velden, Monique G.M.

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Subclinical effects of long‐chain fatty acid β‐oxidation deficiency on the adult heart: A case‐control magnetic resonance study by Knottnerus, Suzan J. G., Bleeker, Jeannette C., Ferdinandusse, Sacha, Houtkooper, Riekelt H., Langeveld, Mirjam, Nederveen, Aart J., Strijkers, Gustav J., Visser, Gepke, Wanders, Ronald J. A., Wijburg, Frits A., Boekholdt, S. Matthijs, Bakermans, Adrianus J.

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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation by Verkerk, Arie O, Knottnerus, Suzan J G, Portero, Vincent, Bleeker, Jeannette C, Ferdinandusse, Sacha, Guan, Kaomei, IJlst, Lodewijk, Visser, Gepke, Wanders, Ronald J A, Wijburg, Frits A, Bezzina, Connie R, Mengarelli, Isabella, Houtkooper, Riekelt H

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