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Lu, Z., Zhang, R., Diasio, R.B., 1993, Dihydropyrimidine dehydrogenase activity in human peripheral blood mononuclear cells and liver: population characteristics, newly identified deficient patients, and clinical implication in 5-fluorouracil chemotherapy. Cancer Res. 55:5433–5438
Wei, X., McLeod, H.L., McMurrough, J., Gonzalez, F.J., Fernandez-Salguero, P., 1996, Molecular basis of the human dihydropyrimidine dehydrogenase deficiency and 5-fluorouracil toxicity. J. Clin. Invest. 98:610–615.
Van Kuilenburg, A.B.P., Vreken, P., Beex, L.V.A.M., Meinsma, J.R., Van Lenthe, H., De Abreu, R.A., Van Gennip, A H., 1997, Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity. Eur. J. Cancer 13:2258–2264.
Sumi, S., Imaeda, M., Kidouchi, K., Ohba, S., Hamajima, N., Kodama, K., Togari, H., Wada, Y., 1998, Population and family studies of dihydropyrimidinuria — prevalence, inheritance mode, and risk of fluorouracil toxicity. Am. J. Med. Gen. 78(4):336–340.
Van Gennip, A.H., Busch, S., Elzinga, L., Stroomer, A.E.M., Van Cruchten, A.C., Scholten, E.G., Abeling, N.G.G.M., 1993, Application of simple chromatographic methods for the diagnosis of defects in pyrimidine degradation. Clin. Chem. 39:380–385.
Van Gennip, A.H., 1990, Screening for inborn errors of purine and pyrimidine metabolism by bi-dimensional TLC and HPLC. In: CRC handbook of chromatography, (Zweig, G., Sherma, J., eds), Molume I: Part A, Nucleic acids and related compounds, Boca Ration: CRC press, pp.22l–245.
Simmonds, H.A., Duley, J.A., Davies, P.M., 1991, Analysis of purines and pyrimidines in blood, urine, and other physiological fluids. In: Techniques in diagnostic human biochemical genetics: A 1aboratorty manual (Hommes, F.A., ed). New York: Wiley-Liss, pp.397–424.
Duran, M., Dorland, L., Meulemann, E.E.E., Allers, P., Berger, R., 1997, Inherited defects of purine and pyrimidine metabolism: Laboratory methods for diagnosis. J. Inher. Metab. Dis. 20:227–236.
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Van Gennip, A.H. et al. (2002). HPLC/ESI Tandem-MS of Liquid Urine or Urine Soaked Filter-Paper Strips for the Detection of Thymine-Uraciluria and Dihydropyrimidinuria. In: Zoref-Shani, E., Sperling, O. (eds) Purine and Pyrimidine Metabolism in Man X. Advances in Experimental Medicine and Biology, vol 486. Springer, Boston, MA. https://doi.org/10.1007/0-306-46843-3_72
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DOI: https://doi.org/10.1007/0-306-46843-3_72
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