Wanders RJA - Search Results

1

Enantiomer-specific pharmacokinetics of D,L-3-hydroxybutyrate: Implications for the treatment of multiple acyl-CoA dehydrogenase deficiency.

van Rijt WJ, Van Hove JLK, Vaz FM, Havinga R, Allersma DP, Zijp TR, Bedoyan JK, Heiner-Fokkema MR, Reijngoud DJ, Geraghty MT, Wanders RJA, Oosterveer MH, Derks TGJ. van Rijt WJ, et al. Among authors: wanders rja. J Inherit Metab Dis. 2021 Jul;44(4):926-938. doi: 10.1002/jimd.12365. Epub 2021 Feb 15. J Inherit Metab Dis. 2021. PMID: 33543789 Free PMC article.

2

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.

Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.

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. 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. J Inherit Metab Dis. 1992;15(3):356-8. doi: 10.1007/BF02435975. J Inherit Metab Dis. 1992. PMID: 1405469 No abstract available.

5

X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect.

Wanders RJ, van Roermund CW, Lageweg W, Jakobs BS, Schutgens RB, Nijenhuis AA, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(4):634-44. doi: 10.1007/BF01799620. J Inherit Metab Dis. 1992. PMID: 1528022 Review.

6

Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.

van Roermund CW, Brul S, Tager JM, Schutgens RB, Wanders RJ. van Roermund CW, et al. J Inherit Metab Dis. 1991;14(2):152-64. doi: 10.1007/BF01800588. J Inherit Metab Dis. 1991. PMID: 1679469

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. 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. 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: 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. J Inherit Metab Dis. 1991;14(3):325-8. doi: 10.1007/BF01811694. J Inherit Metab Dis. 1991. PMID: 1770784 No abstract available.

10

Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: implications for Zellweger syndrome.

Wanders RJ, van Roermund CW, Jakobs C, ten Brink HJ. Wanders RJ, et al. J Inherit Metab Dis. 1991;14(3):349-52. doi: 10.1007/BF01811700. J Inherit Metab Dis. 1991. PMID: 1770789 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

720 results

Search Page