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Table representation of search results timeline featuring number of search results per year.

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
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78 results
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Page 1
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.
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.
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.
78 results