Vreken P[au] - Search Results

Year	Number of Results
1987	1
1988	1
1991	1
1992	2
1993	1
1995	1
1996	1
1997	7
1998	17
1999	15
2000	11
2001	9
2002	5
2003	5
2005	1
2023	0

1

Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.

Ferdinandusse S, Overmars H, Denis S, Waterham HR, Wanders RJ, Vreken P. Ferdinandusse S, et al. Among authors: vreken p. J Lipid Res. 2001 Jan;42(1):137-41. J Lipid Res. 2001. PMID: 11160375 Free article.

2

The rate-limiting step in yeast PGK1 mRNA degradation is an endonucleolytic cleavage in the 3'-terminal part of the coding region.

Vreken P, Raué HA. Vreken P, et al. Mol Cell Biol. 1992 Jul;12(7):2986-96. doi: 10.1128/mcb.12.7.2986-2996.1992. Mol Cell Biol. 1992. PMID: 1320194 Free PMC article.

3

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060.

Barth PG, Wanders RJ, Vreken P. Barth PG, et al. Among authors: vreken p. J Pediatr. 1999 Sep;135(3):273-6. doi: 10.1016/s0022-3476(99)70118-6. J Pediatr. 1999. PMID: 10484787 Review. No abstract available.

4

Disorders of mitochondrial fatty acyl-CoA beta-oxidation.

Wanders RJ, Vreken P, den Boer ME, Wijburg FA, van Gennip AH, IJlst L. Wanders RJ, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 Jun;22(4):442-87. doi: 10.1023/a:1005504223140. J Inherit Metab Dis. 1999. PMID: 10407780 Review.

5

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).

Barth PG, Wanders RJ, Vreken P, Janssen EA, Lam J, Baas F. Barth PG, et al. Among authors: vreken p. J Inherit Metab Dis. 1999 Jun;22(4):555-67. doi: 10.1023/a:1005568609936. J Inherit Metab Dis. 1999. PMID: 10407787 Review.

6

Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.

Van Kuilenburg AB, Vreken P, Abeling NG, Bakker HD, Meinsma R, Van Lenthe H, De Abreu RA, Smeitink JA, Kayserili H, Apak MY, Christensen E, Holopainen I, Pulkki K, Riva D, Botteon G, Holme E, Tulinius M, Kleijer WJ, Beemer FA, Duran M, Niezen-Koning KE, Smit GP, Jakobs C, Smit LM, Van Gennip AH, et al. Van Kuilenburg AB, et al. Among authors: vreken p. Hum Genet. 1999 Jan;104(1):1-9. doi: 10.1007/pl00008711. Hum Genet. 1999. PMID: 10071185 Review.

7

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.

8

Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases.

Wanders RJ, Vreken P, Ferdinandusse S, Jansen GA, Waterham HR, van Roermund CW, Van Grunsven EG. Wanders RJ, et al. Among authors: vreken p. Biochem Soc Trans. 2001 May;29(Pt 2):250-67. doi: 10.1042/0300-5127:0290250. Biochem Soc Trans. 2001. PMID: 11356164 Review.

9

Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong.

Tang NL, Hui J, Law LK, To KF, Mak TW, Cheung KL, Vreken P, Wanders RJ, Fok TF. Tang NL, et al. Among authors: vreken p. Clin Chim Acta. 2001 Nov;313(1-2):195-201. doi: 10.1016/s0009-8981(01)00673-8. Clin Chim Acta. 2001. PMID: 11694259 Review.

10

Isoforms of human CTP synthetase.

van Kuilenburg AB, Meinsma R, Vreken P, Waterham HR, van Gennip AH. van Kuilenburg AB, et al. Among authors: vreken p. Adv Exp Med Biol. 2000;486:257-61. doi: 10.1007/0-306-46843-3_50. Adv Exp Med Biol. 2000. PMID: 11783495 No abstract available.

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