Wanders RJ - Search Results

1

X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management.

Engelen M, Kemp S, de Visser M, van Geel BM, Wanders RJ, Aubourg P, Poll-The BT. Engelen M, et al. Among authors: wanders rj. Orphanet J Rare Dis. 2012 Aug 13;7:51. doi: 10.1186/1750-1172-7-51. Orphanet J Rare Dis. 2012. PMID: 22889154 Free PMC article.

2

Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders.

ten Brink HJ, Schor DS, Kok RM, Poll-The BT, Wanders RJ, Jakobs C. ten Brink HJ, et al. Among authors: wanders rj. J Lipid Res. 1992 Oct;33(10):1449-57. J Lipid Res. 1992. PMID: 1385561 Free article.

3

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.

4

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.

5

Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase.

ten Brink HJ, Poll-The BT, Saudubray JM, Wanders RJ, Jakobs C. ten Brink HJ, et al. Among authors: wanders rj. J Inherit Metab Dis. 1991;14(5):681-4. doi: 10.1007/BF01799934. J Inherit Metab Dis. 1991. PMID: 1779614

6

Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.

Wanders RJ, van Roermund CW, van Wijland MJ, Heikoop J, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Poll-Thé BT, Saudubray JM, et al. Wanders RJ, et al. Clin Chim Acta. 1987 Jul 15;166(2-3):255-63. doi: 10.1016/0009-8981(87)90428-1. Clin Chim Acta. 1987. PMID: 2441904

7

Bile acids in peroxisomal disorders.

Van Eldere JR, Parmentier GG, Eyssen HJ, Wanders RJ, Schutgens RB, Vamecq J, Van Hoof F, Poll-The BT, Saudubray JM. Van Eldere JR, et al. Among authors: wanders rj. Eur J Clin Invest. 1987 Oct;17(5):386-90. doi: 10.1111/j.1365-2362.1987.tb01131.x. Eur J Clin Invest. 1987. PMID: 2446876

8

Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease.

Wanders RJ, Heymans HS, Schutgens RB, Poll-Thé BT, Saudubray JM, Tager JM, Schrakamp G, van den Bosch H. Wanders RJ, et al. J Neurol Sci. 1988 Apr;84(2-3):147-55. doi: 10.1016/0022-510x(88)90120-7. J Neurol Sci. 1988. PMID: 2454298

9

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW, et al. Poll-The BT, et al. Among authors: wanders rj. Am J Hum Genet. 1988 Mar;42(3):422-34. Am J Hum Genet. 1988. PMID: 2894756 Free PMC article.

10

Peroxisomal disorders: concentrations of metabolites in cerebrospinal fluid compared with plasma.

ten Brink HJ, van den Heuvel CM, Poll-The BT, Wanders RJ, Jakobs C. ten Brink HJ, et al. Among authors: wanders rj. J Inherit Metab Dis. 1993;16(3):587-90. doi: 10.1007/BF00711689. J Inherit Metab Dis. 1993. PMID: 7609459 Clinical Trial. No abstract available.

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