Wanders R - Search Results

1

Biochemical aspects of X-linked adrenoleukodystrophy.

Kemp S, Wanders R. Kemp S, et al. Among authors: wanders r. Brain Pathol. 2010 Jul;20(4):831-7. doi: 10.1111/j.1750-3639.2010.00391.x. Brain Pathol. 2010. PMID: 20626744 Free PMC article. Review.

2

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.

3

Peroxisomal fatty acid beta-oxidation in relation to adrenoleukodystrophy.

Wanders RJ, Tager JM. Wanders RJ, et al. Dev Neurosci. 1991;13(4-5):262-6. doi: 10.1159/000112171. Dev Neurosci. 1991. PMID: 1817031 Review.

4

Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids.

Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, van den Bosch H, Schram AW, Tager JM. Wanders RJ, et al. Biochem Biophys Res Commun. 1988 Jun 16;153(2):618-24. doi: 10.1016/s0006-291x(88)81140-9. Biochem Biophys Res Commun. 1988. PMID: 3382393

5

X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.

Wanders RJ, van Roermund CW, van Wijland MJ, Nijenhuis AA, Tromp A, Schutgens RB, Brouwer-Kelder EM, Schram AW, Tager JM, van den Bosch H, et al. Wanders RJ, et al. Clin Chim Acta. 1987 Jun 15;165(2-3):321-9. doi: 10.1016/0009-8981(87)90177-x. Clin Chim Acta. 1987. PMID: 3652454

6

A misdiagnosis of X-linked adrenoleukodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acids.

Gray RG, Green A, Cole T, Davidson V, Giles M, Schutgens RB, Wanders RJ. Gray RG, et al. Among authors: wanders rj. Prenat Diagn. 1995 May;15(5):486-90. doi: 10.1002/pd.1970150514. Prenat Diagn. 1995. PMID: 7644440

7

Clinical and biochemical characteristics of peroxisomal disorders: an update.

Wanders RJ, Barth PG, Schutgens RB, Tager JM. Wanders RJ, et al. Eur J Pediatr. 1994;153(7 Suppl 1):S44-8. doi: 10.1007/BF02138777. Eur J Pediatr. 1994. PMID: 7957386 Review.

8

Delay in diagnosis of X-linked adrenoleukodystrophy.

van Geel BM, Assies J, Haverkort EB, Barth PG, Wanders RJ, Schutgens RB, Keyser A, Zwetsloot CP. van Geel BM, et al. Among authors: wanders rj. Clin Neurol Neurosurg. 1993 Jun;95(2):115-20. doi: 10.1016/0303-8467(93)90004-z. Clin Neurol Neurosurg. 1993. PMID: 8344008

9

Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.

Schutgens RB, Bouman IW, Nijenhuis AA, Wanders RJ, Frumau ME. Schutgens RB, et al. Among authors: wanders rj. Clin Chem. 1993 Aug;39(8):1632-7. Clin Chem. 1993. PMID: 8353949

10

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ. Kemp S, et al. Among authors: wanders rj. J Inherit Metab Dis. 1996;19(5):667-74. doi: 10.1007/BF01799844. J Inherit Metab Dis. 1996. PMID: 8892025

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