Crop residue management and oxalate-extractable iron and aluminium explain long-term soil organic carbon sequestration and dynamics von Van De Vreken, P., Gobin, A., Baken, S., Van Holm, L., Verhasselt, A., Smolders, E., Merckx, R.

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An exponential change decline function to estimate soil organic carbon stocks and their changes from topsoil measurements von Ottoy, S., Elsen, A., Van De Vreken, P., Gobin, A., Merckx, R., Hermy, M., Van Orshoven, J.

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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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Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency von VAN KUILENBURG, A. B. P, VREKEN, P, CHRISTENSEN, E, HOLOPAINEN, I, PULKKI, K, RIVA, D, BOTTEON, G, HOLME, E, TULINIUS, M, KLEIJER, W. J, BEEMER, F. A, DURAN, M, ABELING, N. G. G. M, NIEZEN-KONING, K. E, SMIT, G. P. A, JAKOBS, C, SMIT, L. M. E, MOOG, U, SPAAPEN, L. J. M, VAN GENNIP, A. H, BAKKER, H. D, MEINSMA, R, VAN LENTHE, H, DE ABREU, R. A, SMEITINK, J. A. M, KAYSERILI, H, APAK, M. Y

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Peroxisomal D-hydroxyacyl-CoA Dehydrogenase Deficiency: Resolution of the Enzyme Defect and Its Molecular Basis in Bifunctional Protein Deficiency von Van Grunsven, Elisabeth G., Van Berkel, Emanuel, Ijlst, Lodewijk, Vreken, Peter, Johannis B. C. De Klerk, Adamski, Jerzy, Lemonde, Hugh, Clayton, Peter T., Cuebas, Dean A., Ronald J. A. Wanders

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Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity von Van Kuilenburg, A.B.P., Vreken, P., Beex, L.V.A.M., Meinsma, R., Van Lenthe, H., De Abreu, R.A., Van Gennip, A.H.

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Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene von Hamajima, Naoki, Kouwaki, Masanori, Vreken, Peter, Matsuda, Kouichi, Sumi, Satoshi, Imaeda, Masayuki, Ohba, Satoru, Kidouchi, Kiyoshi, Nonaka, Masaru, Sasaki, Makoto, Tamaki, Nanaya, Endo, Yuichi, De Abreu, Ronnie, Rotteveel, Jan, van Kuilenburg, André, van Gennip, Albert, Togari, Hajime, Wada, Yoshiro

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A point mutation in an invariant splice donor site leads to exon skipping in two unrelated Dutch patients with dihydropyrimidine dehydrogenase deficiency von Vreken, P., Van Kuilenburg, A. B. P., Meinsma, R., Smit, G. P. A., Bakker, H. D., De Abreu, R. A., Gennip, A. H.

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Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: no association with neuroaxonal dystrophy? von Bakker, H D, de Sonnaville, M L, Vreken, P, Abeling, N G, Groener, J E, Keulemans, J L, van Diggelen, O P

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Identification of a four-base deletion (deITCAT296-299) in the dihydropyrimidine dehydrogenase gene with variable clinical expression von VREKEN, P, VAN KUILENBURG, A. B. P, MEINSMA, R, DE ABREU, R. A, VAN GENNIP, A. H

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Severe 5‐fluorouracil toxicity caused by reduced dihydropyrimidine dehydrogenase activity due to heterozygosity for a G→A point mutation von Kuilenburg, A. B. P., Vreken, P., Beex, L. V. A. M., De Abreu, R. A., Gennip, A. H.

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Dihydropyrimidine dehydrogenase deficiency: A novel mutation and expression of missense mutations in E. coli von VREKEN, P, VAN KUILENBURG, A. B. P, MEINSMA, R, BEEMER, F. A, DURAN, M, VAN GENNIP, A. H

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Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria von Gennip, A. H., Abreu, R. A., Lenthe, H., Bakkeren, J., Rotteveel, J., Vreken, P., Kuilenburg, A. B. P.

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Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria von VAN GENNIP, A. H, DE ABREU, R. A, VAN LENTHE, H, BAKKEREN, J, ROTTEVEEL, J, VREKEN, P, VAN KUILENBURG, A. B. P

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Human [alpha]-N-acetylgalactosaminidase ([alpha]-NAGA) deficiency: no association with neuroaxonal dystrophy? von Bakker, Henk D, Marie-Louise CS de Sonnaville, Vreken, Peter, Abeling, Nico GGM, Groener, Johanna EM, Keulemans, Joke LM, van Diggelen, Otto P

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Clinical and biochemical aspects of dihydropyrimidinase deficiency von van Gennip, A.H., de Abreu, R.A., Hoffmann, G.F., Vreken, P., van Kuilenburg, A.B.P.

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Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity von Van Kuilenburg, A.B.P., Vreken, P., Beex, L.V.A.M., Meinsma, R., van Lenthe, H., De Abreu, R.A., Van Gennip, A.H.

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Turnover rate of yeast PGK mRNA can be changed by specific alterations in its trailer structure von Vreken, P., van der Veen, R., de Regt, V.C.H.F., de Maat, A.L., Planta, R.J., Raué, H.A.

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Substituted indolepyridinium as anti-infective compounds von KESTELEYN BART R.R, VAN DE VREKEN WIM, DE VROEY VERONIQUE CORINE P, KINDERMANS NATALIE M.F, JOCHMANS DIRK E.D, HERTOGS KURT, BETTENS EVA, CANARD MAXIME FRANCIS J

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Neerlandia. Jaargang 21 von [tijdschrift] Neerlandia

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