Ijlst L - Search Results

1

[Short-chain acyl-CoA dehydrogenase deficiency (SCADD): relatively high prevalence in the Netherlands and strongly variable fenotype; neonatal screening not indicated].

van Maldegem BT, Duran M, Wanders RJ, Niezen-Koning KE, Hogeveen M, Ijlst L, Waterham HR, Wijburg FA. van Maldegem BT, et al. Among authors: ijlst l. Ned Tijdschr Geneeskd. 2008 Jul 26;152(30):1678-85. Ned Tijdschr Geneeskd. 2008. PMID: 18714522 Dutch.

2

A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS.

Niezen-Koning KE, Wanders RJ, Nagel GT, IJlst L, Heymans HS. Niezen-Koning KE, et al. Among authors: ijlst l. Biochim Biophys Acta. 1992 Oct 13;1180(1):28-32. doi: 10.1016/0925-4439(92)90023-g. Biochim Biophys Acta. 1992. PMID: 1390941

3

Long-chain 3-hydroxyacyl-CoA dehydrogenase in leukocytes and chorionic villus fibroblasts: potential for pre- and postnatal diagnosis.

Wanders RJ, Ijlst L. Wanders RJ, et al. Among authors: ijlst l. J Inherit Metab Dis. 1992;15(3):356-8. doi: 10.1007/BF02435975. J Inherit Metab Dis. 1992. PMID: 1405469 No abstract available.

4

Molecular analysis of disorders of peroxisomal beta-oxidation.

Wanders RJ, van Roermund CW, Denis S, Schutgens RB, Ijlst L, Tager JM. Wanders RJ, et al. Among authors: ijlst l. Prog Clin Biol Res. 1992;375:507-19. Prog Clin Biol Res. 1992. PMID: 1438395 Review. No abstract available.

5

Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidation.

Wanders RJ, IJlst L, Poggi F, Bonnefont JP, Munnich A, Brivet M, Rabier D, Saudubray JM. Wanders RJ, et al. Among authors: ijlst l. Biochem Biophys Res Commun. 1992 Nov 16;188(3):1139-45. doi: 10.1016/0006-291x(92)91350-y. Biochem Biophys Res Commun. 1992. PMID: 1445348

6

Fatty acid beta-oxidation in leukocytes from control subjects and medium-chain acyl-CoA dehydrogenase deficient patients.

Wanders RJ, Ijlst L. Wanders RJ, et al. Among authors: ijlst l. Biochim Biophys Acta. 1992 Jan 16;1138(1):80-4. doi: 10.1016/0925-4439(92)90155-g. Biochim Biophys Acta. 1992. PMID: 1737072

7

Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disorders.

Wanders RJ, Ijlst L, van Elk E, de Klerk JB, Przyrembel H. Wanders RJ, et al. Among authors: ijlst l. J Inherit Metab Dis. 1991;14(3):317-20. doi: 10.1007/BF01811692. J Inherit Metab Dis. 1991. PMID: 1770782 No abstract available.

8

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients.

Wanders RJ, Ijlst L, Duran M, Jakobs C, de Klerk JB, Przyrembel H, Rocchiccioli F, Aubourg P. Wanders RJ, et al. Among authors: ijlst l. J Inherit Metab Dis. 1991;14(3):325-8. doi: 10.1007/BF01811694. J Inherit Metab Dis. 1991. PMID: 1770784 No abstract available.

9

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Przyrembel H, Jakobs C, IJlst L, de Klerk JB, Wanders RJ. Przyrembel H, et al. Among authors: ijlst l. J Inherit Metab Dis. 1991;14(5):674-80. doi: 10.1007/BF01799932. J Inherit Metab Dis. 1991. PMID: 1779613 No abstract available.

10

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.

Duran M, Wanders RJ, de Jager JP, Dorland L, Bruinvis L, Ketting D, Ijlst L, van Sprang FJ. Duran M, et al. Among authors: ijlst l. Eur J Pediatr. 1991 Jan;150(3):190-5. doi: 10.1007/BF01963564. Eur J Pediatr. 1991. PMID: 2044590

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