Genotype-Specific Differences in the Tumor Metabolite Profile of Pheochromocytoma and Paraganglioma Using Untargeted and Targeted Metabolomics
Rao, J. U, Engelke, U. F. H, Sweep, F. C. G. J, Pacak, K, Kusters, B, Goudswaard, A. G, Hermus, A. R. M. M, Mensenkamp, A. R, Eisenhofer, G, Qin, N, Richter, S, Kunst, H. P. M, Timmers, H. J. L. M, Wevers, R. A
Published in The journal of clinical endocrinology and metabolism (01.02.2015)
Published in The journal of clinical endocrinology and metabolism (01.02.2015)
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Journal Article
Regularized MANOVA (rMANOVA) in untargeted metabolomics
Engel, J., Blanchet, L., Bloemen, B., van den Heuvel, L.P., Engelke, U.H.F., Wevers, R.A., Buydens, L.M.C.
Published in Analytica chimica acta (29.10.2015)
Published in Analytica chimica acta (29.10.2015)
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Journal Article
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)
Mochel, F., Sedel, F., Vanderver, A., Engelke, U. F. H., Barritault, J., Yang, B. Z., Kulkarni, B., Adams, D. R., Clot, F., Ding, J. H., Kaneski, C. R., Verheijen, F. W., Smits, B. W., Seguin, F., Brice, A., Vanier, M. T., Huizing, M., Schiffmann, R., Durr, A., Wevers, R. A.
Published in Brain (London, England : 1878) (01.03.2009)
Published in Brain (London, England : 1878) (01.03.2009)
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Journal Article
Elevated CSF N-acetylaspartylglutamate in patients with free sialic acid storage diseases
Mochel, F, Engelke, U F H, Barritault, J, Yang, B, McNeill, N H, Thompson, J N, Vanderver, A, Wolf, N I, Willemsen, M A, Verheijen, F W, Seguin, F, Wevers, R A, Schiffmann, R
Published in Neurology (26.01.2010)
Published in Neurology (26.01.2010)
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Journal Article
The clinical relevance of novel biomarkers as outcome parameter in adults with phenylketonuria
Wegberg, A. M. J., Weerd, J. C., Engelke, U. F. H., Coene, K. L. M., Jahja, R., Bakker, S. J. L., Huijbregts, S. C. J., Wevers, R. A., Heiner‐Fokkema, M. R., Spronsen, F. J.
Published in Journal of inherited metabolic disease (01.07.2024)
Published in Journal of inherited metabolic disease (01.07.2024)
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Journal Article
Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidine
Wevers, R. A., Christensen, M., Engelke, U. F. H., Geuer, S., Coene, K. L. M., Kwast, J. T., Lund, A. M., Vissers, L. E. L. M.
Published in Journal of inherited metabolic disease (01.05.2019)
Published in Journal of inherited metabolic disease (01.05.2019)
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Journal Article
Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolism
MOOLENAAR, S. H, ENGELKE, U. F. H, WEVERS, R. A
Published in Annals of Clinical Biochemistry (01.01.2003)
Published in Annals of Clinical Biochemistry (01.01.2003)
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Book Review
Journal Article
Leukoencephalopathy associated with a disturbance in the metabolism of polyols
Van Der Knaap, M. S., Wevers, R. A., Struys, E. A., Verhoeven, N. M., Pouwels, P. J. W., Engelke, U. F. H., Feikema, W., Valk, J., Jakobs, C.
Published in Annals of neurology (01.12.1999)
Published in Annals of neurology (01.12.1999)
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Journal Article
Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine
Moolenaar, S. H., Engelke, U. F. H., Abeling, N. G. G. M., Mandel, H., Duran, M., Wevers, R. A.
Published in Journal of inherited metabolic disease (01.12.2001)
Published in Journal of inherited metabolic disease (01.12.2001)
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Journal Article
Defect in Dimethylglycine Dehydrogenase, a New Inborn Error of Metabolism: NMR Spectroscopy Study
Moolenaar, Sytske H, Poggi-Bach, Jo, Engelke, Udo F.H, Corstiaensen, Jacqueline M.B, Heerschap, Arend, de Jong, Jan G.N, Binzak, Barbara A, Vockley, Jerry, Wevers, Ron A
Published in Clinical chemistry (Baltimore, Md.) (01.04.1999)
Published in Clinical chemistry (Baltimore, Md.) (01.04.1999)
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Journal Article
Prolidase deficiency diagnosed by ^sup 1^H NMR spectroscopy of urine
Moolenaar, S H, Engelke, U F H, N G G M Abeling, Mandel, H
Published in Journal of inherited metabolic disease (01.12.2001)
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Published in Journal of inherited metabolic disease (01.12.2001)
Journal Article
Prolidase deficiency diagnosed by 1 H NMR spectroscopy of urine
Moolenaar, S. H., Engelke, U. F. H., Abeling, N. G. G. M., Mandel, H., Duran, M., Wevers, R. A.
Published in Journal of inherited metabolic disease (01.12.2001)
Published in Journal of inherited metabolic disease (01.12.2001)
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Journal Article
1H-NMR spectroscopy of body fluids : Inborn errors of purine and pyrimidine metabolism
WEVERS, R. A, ENGELKE, U. F. H, MOOLENAAR, S. H, BRÄUTIGAM, C, DE JONG, J. G. N, DURAN, R, DE ABREU, R. A, VAN GENNIP, A. H
Published in Clinical chemistry (Baltimore, Md.) (01.04.1999)
Published in Clinical chemistry (Baltimore, Md.) (01.04.1999)
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