Genotype-Specific Differences in the Tumor Metabolite Profile of Pheochromocytoma and Paraganglioma Using Untargeted and Targeted Metabolomics von 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

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Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axis von van der Doelen, R H A, Deschamps, W, D'Annibale, C, Peeters, D, Wevers, R A, Zelena, D, Homberg, J R, Kozicz, T

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Mevalonate kinase deficiency: Evidence for a phenotypic continuum von SIMON, A, KREMER, H. P. H, WEVERS, R. A, SCHEFFER, H, DE JONG, J. G, VAN DER MEER, J. W. M, DRENTH, J. P. H

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3-Methylglutaconic aciduria type I redefined: A syndrome with late-onset leukoencephalopathy von WORTMANN, S. B, KREMER, B. H, WILCKEN, B, CRUYSBERG, J. R, DAS, A. M, MORAVA, E, WEVERS, R. A, GRAHAM, A, WILLEMSEN, M. A, LOUPATTY, F. J, HOGG, S. L, ENGELKE, U. F, KLUIJTMANS, L. A, WANDERS, R. J, ILLSINGER, S

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Ophthalmological abnormalities in children with congenital disorders of glycosylation type I von Morava, E, Wosik, H N, Sykut-Cegielska, J, Adamowicz, M, Guillard, M, Wevers, R A, Lefeber, D J, Cruysberg, J R M

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Identification of Pseudomonas aeruginosa and Aspergillus fumigatus mono- and co-cultures based on volatile biomarker combinations von Neerincx, A H, Geurts, B P, Habets, M F J, Booij, J A, van Loon, J, Jansen, J J, Buydens, L M C, van Ingen, J, Mouton, J W, Harren, F J M, Wevers, R A, Merkus, P J F M, Cristescu, S M, Kluijtmans, L A J

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Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency von SCHILLER, A, WEVERS, R. A, STEENBERGEN, G. C. H, BLAU, N, JUNG, H. H

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Glycosylation defects underlying fetal alcohol spectrum disorder: a novel pathogenetic model von Binkhorst, M., Wortmann, S. B., Funke, S., Kozicz, T., Wevers, R. A., Morava, E.

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Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency? von ORNGREEN, M. C, SCHELHAAS, H. J, JEPPESEN, T. D, AKMAN, H. O, WEVERS, R. A, ANDERSEN, S. T, TER LAAK, H. J, VAN DIGGELEN, O. P, DIMAURO, S, VISSING, J

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Elevated CSF N-acetylaspartylglutamate in patients with free sialic acid storage diseases von MOCHEL, F, ENGELKE, U. F. H, SEGUIN, F, WEVERS, R. A, SCHIFFMANN, R, BARRITAULT, J, YANG, B, MCNEILL, N. H, THOMPSON, J. N, VANDERVER, A, WOLF, N. I, WILLEMSEN, M. A, VERHEIJEN, F. W

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Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA) von 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.

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Dopa-responsive dystonia: A clinical and molecular genetic study von Bandmann, O., Valente, E. M., Holmans, P., Surtees, R. A. H., Walters, J. H., Wevers, R. A., Marsden, C. D., Wood, N. W.

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Regularized MANOVA (rMANOVA) in untargeted metabolomics von Engel, J., Blanchet, L., Bloemen, B., van den Heuvel, L.P., Engelke, U.H.F., Wevers, R.A., Buydens, L.M.C.

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Cerebrotendinous xanthomatosis without neurological involvement von Stelten, B. M. L., Raal, F. J., Marais, A. D., Riksen, N. P., Roeters van Lennep, J. E., Duell, P.B, Graaf, M., Kluijtmans, L. A. J., Wevers, R. A., Verrips, A.

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Substrate deprivation therapy in juvenile Sandhoff disease von Wortmann, S. B., Lefeber, D. J., Dekomien, G., Willemsen, M. A. A. P., Wevers, R. A., Morava, E.

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Thrombotic complications in patients with PMM2-CDG von Linssen, M., Mohamed, M., Wevers, R.A., Lefeber, D.J., Morava, E.

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The clinical relevance of novel biomarkers as outcome parameter in adults with phenylketonuria von 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.

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Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene von Waterham, Hans R., Wijburg, Frits A., Hennekam, Raoul C.M., Vreken, Peter, Poll-The, Bwee Tien, Dorland, Lambertus, Duran, Marinus, Jira, Petr E., Smeitink, Jan A.M., Wevers, Ron A., Wanders, Ronald J.A.

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Clinical and biochemical presentation of siblings with COG‐7 deficiency, a lethal multiple O‐ and N‐glycosylation disorder von Spaapen, L. J. M., Bakker, J. A., der Meer, S. B., Sijstermans, H. J., Steet, R. A., Wevers, R. A., Jaeken, J.

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Congenital disorder of glycosylation type Ix: Review of clinical spectrum and diagnostic steps von Morava, É., Wosik, H., Kárteszi, J., Guillard, M., Adamowicz, M., Sykut-Cegielska, J., Hadzsiev, K., Wevers, R. A., Lefeber, D. J.

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