Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency von Bleeker, Jeannette C., Visser, Gepke, Clarke, Kieran, Ferdinandusse, Sacha, Haan, Ferdinand H., Houtkooper, Riekelt H., IJlst, Lodewijk, Kok, Irene L., Langeveld, Mirjam, Pol, W. Ludo, Sain‐van der Velden, Monique G. M., Sibeijn‐Kuiper, Anita, Takken, Tim, Wanders, Ronald J. A., Weeghel, Michel, Wijburg, Frits A., Woude, Luc H., Wüst, Rob C. I., Cox, Pete J., Jeneson, Jeroen A. L.

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Impact of newborn screening for very‐long‐chain acyl‐CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes von Bleeker, Jeannette C., Kok, Irene L., Ferdinandusse, Sacha, van der Pol, W. Ludo, Cuppen, Inge, Bosch, Annet M., Langeveld, Mirjam, Derks, Terry G. J., Williams, Monique, de Vries, Maaike, Mulder, Margot F., Gozalbo, Estela R., de Sain‐van der Velden, Monique G. M., Rennings, Alexander J., Schielen, Peter J. C. I., Dekkers, Eugenie, Houtkooper, Riekelt H., Waterham, Hans R., Pras‐Raves, Mia L., Wanders, Ronald J. A., van Hasselt, Peter M., Schoenmakers, Marja, Wijburg, Frits A., Visser, Gepke

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Misdiagnosis of CTX due to propofol: The interference of total intravenous propofol anaesthesia with bile acid profiling von Claesen, Joep L. A., Koomen, Erik, Schene, Imre F., Jans, Judith J. M., Mast, Natalia, Pikuleva, Irina A., Ham, Maria, Velden, Monique G. M., Fuchs, Sabine A.

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Direct Infusion Based Metabolomics Identifies Metabolic Disease in Patients' Dried Blood Spots and Plasma von Haijes, Hanneke A, Willemsen, Marcel, Van der Ham, Maria, Gerrits, Johan, Pras-Raves, Mia L, Prinsen, Hubertus C M T, Van Hasselt, Peter M, De Sain-van der Velden, Monique G M, Verhoeven-Duif, Nanda M, Jans, Judith J M

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Vitamin B6 in plasma and cerebrospinal fluid of children von Albersen, Monique, Bosma, Marjolein, Jans, Judith J M, Hofstede, Floris C, van Hasselt, Peter M, de Sain-van der Velden, Monique G M, Visser, Gepke, Verhoeven-Duif, Nanda M

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Pyridoxine or pyridoxal‐5‐phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort study von Bayat, Allan, Aledo‐Serrano, Angel, Gil‐Nagel, Antonio, Korff, Christian M., Thomas, Ashley, Boßelmann, Christian, Weber, Yvonne, Gardella, Elena, Lund, Allan M, Sain‐van der Velden, Monique G. M., Møller, Rikke S

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Identification of human D lactate dehydrogenase deficiency von Monroe, Glen R., van Eerde, Albertien M., Tessadori, Federico, Duran, Karen J., Savelberg, Sanne M. C., van Alfen, Johanna C., Terhal, Paulien A., van der Crabben, Saskia N., Lichtenbelt, Klaske D., Fuchs, Sabine A., Gerrits, Johan, van Roosmalen, Markus J., van Gassen, Koen L., van Aalderen, Mirjam, Koot, Bart G., Oostendorp, Marlies, Duran, Marinus, Visser, Gepke, de Koning, Tom J., Calì, Francesco, Bosco, Paolo, Geleijns, Karin, de Sain-van der Velden, Monique G. M., Knoers, Nine V., Bakkers, Jeroen, Verhoeven-Duif, Nanda M., van Haaften, Gijs, Jans, Judith J.

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A Delphi Survey Study to Formulate Statements on the Treatability of Inherited Metabolic Disorders to Decide on Eligibility for Newborn Screening von Veldman, Abigail, Kiewiet, M. B. Gea, Westra, Dineke, Bosch, Annet M, Brands, Marion M. G, de Coo, René I. F. M, Derks, Terry G. J, Fuchs, Sabine A, van den Hout, Johanna. M. P, Huidekoper, Hidde H, Kluijtmans, Leo A. J, Koop, Klaas, Lubout, Charlotte M. A, Mulder, Margaretha F, Panis, Bianca, Rubio-Gozalbo, M. Estela, de Sain-van der Velden, Monique G, Schaefers, Jaqueline, Schreuder, Andrea B, Visser, Gepke, Wevers, Ron A, Wijburg, Frits A, Heiner-Fokkema, M. Rebecca, van Spronsen, Francjan J

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Cross-Omics: Integrating Genomics with Metabolomics in Clinical Diagnostics von Kerkhofs, Marten H. P. M., Haijes, Hanneke A., Willemsen, A. Marcel, van Gassen, Koen L. I., van der Ham, Maria, Gerrits, Johan, de Sain-van der Velden, Monique G. M., Prinsen, Hubertus C. M. T., van Deutekom, Hanneke W. M., van Hasselt, Peter M., Verhoeven-Duif, Nanda M., Jans, Judith J. M.

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Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome von Magnée, Maurice J C M, Lamme, Victor A F, de Sain-van der Velden, Monique G M, Vorstman, Jacob A S, Kemner, Chantal

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Quantification of metabolites in dried blood spots by direct infusion high resolution mass spectrometry von de Sain-van der Velden, Monique G.M., van der Ham, Maria, Gerrits, Johan, Prinsen, Hubertus C.M.T., Willemsen, Marcel, Pras-Raves, Mia L., Jans, Judith J., Verhoeven-Duif, Nanda M.

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Optimising urinary catecholamine metabolite diagnostics for neuroblastoma von Matser, Yvette A. H., Verly, Iedan R. N., Ham, Maria, Sain‐van der Velden, Monique G. M., Verhoeven‐Duif, Nanda M., Ash, Shifra, Cangemi, Giuliana, Barco, Sebastiano, Popovic, Maja Beck, Kuilenburg, André B. P., Tytgat, Godelieve A. M., Cañete, Adela, Wieczorek, Aleksandra, Vicha, Ales, Alba, Amparo, Ryan, Anne L, Brichard, Bénédicte, Yalçın, Bilgehan, Martínez, Blanca, Márquez, Catalina, Klapkova, Eva, Schleiermacher, Gudrun, Deubzer, Hedwig, Ryberg, Henrik, Øra, Ingrid, Sastry, Jairam, Bugajska, Jolanta, Gray, Juliet C, Baka, Margarita, Martínez, Maria Luisa, Phillips, Marianne B., Renard, Marleen, Vermeersch, Pieter, Alvaro, Raquel Hladun, Almaraz, Ricardo López, Simon, Thorsten, Ek, Torben, Segura, Vanessa, Papadakis, Vassilios

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Whole body composition analysis by the BodPod air-displacement plethysmography method in children with phenylketonuria shows a higher body fat percentage von Albersen, Monique, Bonthuis, Marjolein, de Roos, Nicole M., van den Hurk, Dorine A. M., Carbasius Weber, Ems, Hendriks, Margriet M. W. B., de Sain-van der Velden, Monique G. M., de Koning, Tom J., Visser, Gepke

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Untargeted Metabolomics for Metabolic Diagnostic Screening with Automated Data Interpretation Using a Knowledge-Based Algorithm von Haijes, Hanneke A., van der Ham, Maria, Prinsen, Hubertus C. M. T., Broeks, Melissa H., van Hasselt, Peter M., de Sain-van der Velden, Monique G. M., Verhoeven-Duif, Nanda M., Jans, Judith J. M.

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Yield of additional metabolic studies in neurodevelopmental disorders von Engbers, Hannelie M., Berger, Ruud, van Hasselt, Peter, de Koning, Tom, de Sain-van der Velden, Monique G. M., Kroes, Hester Y., Visser, Gepke

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Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency von Bleeker, Jeannette C., Kok, Irene L., Ferdinandusse, Sacha, de Vries, Maaike, Derks, Terry G.J., Mulder, Margot F., Williams, Monique, Gozalbo, Estela Rubio, Bosch, Annet M., van den Hurk, Dorine T., de Sain‐van der Velden, Monique G.M., Waterham, Hans R., Wijburg, Frits A., Visser, Gepke

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Metabolic profiles in children during fasting von van Veen, Merel R, van Hasselt, Peter M, de Sain-van der Velden, Monique G M, Verhoeven, Nanda, Hofstede, Floris C, de Koning, Tom J, Visser, Gepke

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Assessment of carnitine excretion and its ratio to plasma free carnitine as a biomarker for primary carnitine deficiency in newborns von Crefcoeur, Loek L., Heiner‐Fokkema, M. Rebecca, Maase, Rose E., Visser, Gepke, Sain‐van der Velden, Monique G. M.

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Liquid chromatography–tandem mass spectrometry assay for the quantification of free and total sialic acid in human cerebrospinal fluid von van der Ham, Maria, de Koning, Tom J., Lefeber, Dirk, Fleer, André, Prinsen, Berthil H.C.M.T., de Sain-van der Velden, Monique G.M.

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Two Mass-Spectrometric Techniques for Quantifying Serine Enantiomers and Glycine in Cerebrospinal Fluid: Potential Confounders and Age-Dependent Ranges von Fuchs, Sabine A, de Sain-van der Velden, Monique G. M, de Barse, Martina M. J, Roeleveld, Martin W, Hendriks, Margriet, Dorland, Lambertus, Klomp, Leo W. J, Berger, Ruud, de Koning, Tom J

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