Vreken P - Search Results

1

Dihydropyrimidine dehydrogenase (DPD) deficiency: identification and expression of missense mutations C29R, R886H and R235W.

Vreken P, Van Kuilenburg AB, Meinsma R, van Gennip AH. Vreken P, et al. Hum Genet. 1997 Dec;101(3):333-8. doi: 10.1007/s004390050637. Hum Genet. 1997. PMID: 9439663

2

A point mutation in an invariant splice donor site leads to exon skipping in two unrelated Dutch patients with dihydropyrimidine dehydrogenase deficiency.

Vreken P, Van Kuilenburg AB, Meinsma R, Smit GP, Bakker HD, De Abreu RA, van Gennip AH. Vreken P, et al. J Inherit Metab Dis. 1996;19(5):645-54. doi: 10.1007/BF01799841. J Inherit Metab Dis. 1996. PMID: 8892022

3

Inborn errors of pyrimidine degradation: clinical, biochemical and molecular aspects.

van Gennip AH, Abeling NG, Vreken P, van Kuilenburg AB. van Gennip AH, et al. Among authors: vreken p. J Inherit Metab Dis. 1997 Jun;20(2):203-13. doi: 10.1023/a:1005356806329. J Inherit Metab Dis. 1997. PMID: 9211193 Review.

4

Identification of a four-base deletion (delTCAT296-299) in the dihydropyrimidine dehydrogenase gene with variable clinical expression.

Vreken P, Van Kuilenburg AB, Meinsma R, De Abreu RA, Van Gennip AH. Vreken P, et al. Hum Genet. 1997 Aug;100(2):263-5. doi: 10.1007/s004390050502. Hum Genet. 1997. PMID: 9254861

5

Identification of novel point mutations in the dihydropyrimidine dehydrogenase gene.

Vreken P, Van Kuilenburg AB, Meinsma R, van Gennip AH. Vreken P, et al. J Inherit Metab Dis. 1997 Jul;20(3):335-8. doi: 10.1023/a:1005357307122. J Inherit Metab Dis. 1997. PMID: 9266349 No abstract available.

6

Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity.

Van Kuilenburg AB, Vreken P, Beex LV, Meinsma R, Van Lenthe H, De Abreu RA, van Gennip AH. Van Kuilenburg AB, et al. Among authors: vreken p. Eur J Cancer. 1997 Nov;33(13):2258-64. doi: 10.1016/s0959-8049(97)00261-x. Eur J Cancer. 1997. PMID: 9470816

7

Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity.

Van Kuilenburg AB, Vreken P, Beex LV, Meinsma R, Van Lenthe H, De Abreu RA, Van Gennip AH. Van Kuilenburg AB, et al. Among authors: vreken p. Adv Exp Med Biol. 1998;431:293-8. doi: 10.1007/978-1-4615-5381-6_58. Adv Exp Med Biol. 1998. PMID: 9598078 No abstract available.

8

Dihydropyrimidine dehydrogenase deficiency. Identification of two novel mutations and expression of missense mutations in E. coli.

Vreken P, van Kuilenburg AB, Meinsma R, van Gennip AH. Vreken P, et al. Adv Exp Med Biol. 1998;431:341-6. Adv Exp Med Biol. 1998. PMID: 9598088 No abstract available.

9

Dihydropyrimidine dehydrogenase deficiency: a novel mutation and expression of missense mutations in E. coli.

Vreken P, van Kuilenburg AB, Meinsma R, Beemer FA, Duran M, van Gennip AH. Vreken P, et al. J Inherit Metab Dis. 1998 Jun;21(3):276-9. doi: 10.1023/a:1005380525218. J Inherit Metab Dis. 1998. PMID: 9686374 No abstract available.

10

Severe 5-fluorouracil toxicity caused by reduced dihydropyrimidine dehydrogenase activity due to heterozygosity for a G-->A point mutation.

van Kuilenburg AB, Vreken P, Beex LV, De Abreu RA, van Gennip AH. van Kuilenburg AB, et al. Among authors: vreken p. J Inherit Metab Dis. 1998 Jun;21(3):280-4. doi: 10.1023/a:1005384609289. J Inherit Metab Dis. 1998. PMID: 9686375 No abstract available.

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