Reduced replication of 3TC‐resistant HIV‐1 variants in primary cells due to a processivity defect of the reverse transcriptase enzyme von Back, N. K., Nijhuis, M., Keulen, W., Boucher, C. A., Oude Essink, B. O., Kuilenburg, A. B., Gennip, A. H., Berkhout, B.

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Disorders of mitochondrial fatty acyl‐CoA β‐oxidation von Wanders, R. J. A., Vreken, P., Boer, M. E. J., Wijburg, F. A., Van Gennip, A. H., IJlst, L.

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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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Quantitative plasma acylcarnitine analysis using electrospray tandem mass spectrometry for the diagnosis of organic acidaemias and fatty acid oxidation defects von Vreken, P., Lint, A. E. M., Bootsma, A. H., Overmars, H., Wanders, R. J. A., Gennip, A. H.

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Clinical features of galactokinase deficiency:A review of the literature von Bosch, A. M., Bakker, H. D., Gennip, A. H., Kempen, J. V., Wanders, R. J. A., Wijburg, F. A.

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Reduced 5-FU clearance in a patient with low DPD activity due to heterozygosity for a mutant allele of the DPYD gene von MARING, J. G, VAN KUILENBURG, A. B. P, HAASJES, J, PIERSMA, H, GROEN, H. J. M, UGES, D. R. A, VAN GENNIP, A. H, DE VRIES, E. G. E

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X-linked borderline mental retardation with prominent behavioral disturbance : phenotype, genetic localization, and evidence for disturbed monoamine metabolism von BRUNNER, H. G, NELEN, M. R, VAN ZANDVOORT, P, ABELING, N. G. G. M, VAN GENNIP, A. H, WOLTERS, E. C, KUIPER, M. A, ROPERS, H. H, VAN OOST, B. A

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Clinical features of galactokinase deficiency: A review of the literature von BOSCH, A. M, BAKKER, H. D, VAN GENNIP, A. H, VAN KEMPEN, J. V, WANDERS, R. J. A, WIJBURG, F. A

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Linoleic acid supplemention of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatment von Valianpour, F., Wanders, R.J.A., Overmars, H., Vaz, F.M., Barth, P.G., van Gennip, A.H.

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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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Rapid Screening of High-Risk Patients for Disorders of Purine and Pyrimidine Metabolism Using HPLC-Electrospray Tandem Mass Spectrometry of Liquid Urine or Urine-soaked Filter Pape... von Ito, Tetsuya, van Kuilenburg, Andre B.P, Bootsma, Albert H, Haasnoot, Anja J, van Cruchten, Arno, Wada, Yoshiro, van Gennip, Albert H

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Pitfalls in the Diagnosis of Patients with a Partial Dihydropyrimidine Dehydrogenase Deficiency von Van Kuilenburg, Andre B.P, Van Lenthe, Henk, Tromp, Annelies, Veltman, Patricia C.J, Van Gennip, Albert H

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Pharmacokinetics of S-1, an oral formulation of ftorafur, oxonic acid and 5-chloro-2,4-dihydroxypyridine (molar ratio 1:0.4:1) in patients with solid tumors von PETERS, G. J, NOORDHUIS, P, HOLWERDA, U, GIACCONE, K. Smid G, FUMOLEAU, P, VAN GROENINGEN, C. J, VAN KUILENBURG, A. B. P, SCHORNAGEL, J. H, GALL, H, TURNER, S. L, SWART, M. S, VOORN, D, VAN GENNIP, A. H, WANDERS, J

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Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: Application for selective screening of peroxisomal disorders von Bootsma, A. H., Overmars, H., Rooij, A., Lint, A. E. M., Wanders, R. J. A., Gennip, A. H., Vreken, P.

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Dihydropyrimidine dehydrogenase deficiency presenting at birth von Al‐Sanna'a, N. A., Van Kuilenburg, A. B. P., Atrak, T. M., Jabbar, M. A. Abdul, Van Gennip, A. H.

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Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspects von Gennip, A.H., Abeling, N.G.G.M., Vreken, P., Kuilenburg, A.B.P.

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Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency von Enns, G. M., Barkovich, A. J., Kuilenburg, A. B. P., Manning, M., Sanger, T., Witt, D. R., Gennip, A. H.

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Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects von Ridge, Susan A., Sludden, Julieann, Brown, Oliver, Robertson, Leigh, Wei, Xiaoxiong, Sapone, Andrea, Fernandez‐Salguero, Pedro M., Gonzalez, Frank J., Vreken, Peter, Van Kuilenburg, Andre BP, Van Gennip, Albert H., McLeod, Howard L.

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Lethal 5-fluorouracil toxicity associated with a novel mutation in the dihydropyrimidine dehydrogenase gene von van Kuilenburg, A. B. P., Baars, J. W., Meinsma, R., van Gennip, A. H.

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Defects in Pyrimidine Degradation Identified by HPLC-Electrospray Tandem Mass Spectrometry of Urine Specimens or Urine-soaked Filter Paper Strips von van Lenthe, Henk, van Kuilenburg, Andre B.P, Ito, Tetsuya, Bootsma, Albert H, van Cruchten, Arno, Wada, Yoshiro, van Gennip, Albert H

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