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beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities.
van Kuilenburg AB, Meinsma R, Beke E, Assmann B, Ribes A, Lorente I, Busch R, Mayatepek E, Abeling NG, van Cruchten A, Stroomer AE, van Lenthe H, Zoetekouw L, Kulik W, Hoffmann GF, Voit T, Wevers RA, Rutsch F, van Gennip AH. van Kuilenburg AB, et al. Among authors: stroomer ae. Hum Mol Genet. 2004 Nov 15;13(22):2793-801. doi: 10.1093/hmg/ddh303. Epub 2004 Sep 22. Hum Mol Genet. 2004. PMID: 15385443
No circadian variation of dihydropyrimidine dehydrogenase, uridine phosphorylase, beta-alanine, and 5-fluorouracil during continuous infusion of 5-fluorouracil.
Van Kuilenburg AB, Poorter RL, Peters GJ, Van Gennip AH, Van Lenthe H, Stroomer AE, Smid K, Noordhuis P, Bakker PJ, Veenhof CH. Van Kuilenburg AB, et al. Among authors: stroomer ae. Adv Exp Med Biol. 1998;431:811-6. doi: 10.1007/978-1-4615-5381-6_156. Adv Exp Med Biol. 1998. PMID: 9598176 No abstract available.
12 results