IJlst L - Search Results

1

Maintenance of cellular vitamin B₆ levels and mitochondrial oxidative function depend on pyridoxal 5'-phosphate homeostasis protein.

Ciapaite J, van Roermund CWT, Bosma M, Gerrits J, Houten SM, IJlst L, Waterham HR, van Karnebeek CDM, Wanders RJA, Zwartkruis FJT, Jans JJ, Verhoeven-Duif NM. Ciapaite J, et al. Among authors: ijlst l. J Biol Chem. 2023 Sep;299(9):105047. doi: 10.1016/j.jbc.2023.105047. Epub 2023 Jul 13. J Biol Chem. 2023. PMID: 37451483 Free PMC article.

2

Genistein in Sanfilippo disease: a randomized controlled crossover trial.

de Ruijter J, Valstar MJ, Narajczyk M, Wegrzyn G, Kulik W, Ijlst L, Wagemans T, van der Wal WM, Wijburg FA. de Ruijter J, et al. Among authors: ijlst l. Ann Neurol. 2012 Jan;71(1):110-20. doi: 10.1002/ana.22643. Ann Neurol. 2012. PMID: 22275257 Clinical Trial.

3

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

4

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.

5

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.

6

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

7

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

8

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.

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

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype.

Ijlst L, Uskikubo S, Kamijo T, Hashimoto T, Ruiter JP, de Klerk JB, Wanders RJ. Ijlst L, et al. J Inherit Metab Dis. 1995;18(2):241-4. doi: 10.1007/BF00711778. J Inherit Metab Dis. 1995. PMID: 7564258 No abstract available.

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