Wanders RJA - Search Results

1

Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disorders.

Herzog K, van Lenthe H, Wanders RJA, Vaz FM, Waterham HR, Ferdinandusse S. Herzog K, et al. Among authors: wanders rja. Mol Genet Metab. 2017 Jul;121(3):279-282. doi: 10.1016/j.ymgme.2017.05.003. Epub 2017 May 6. Mol Genet Metab. 2017. PMID: 28566232

2

Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography.

ten Brink HJ, Stellaard F, van den Heuvel CM, Kok RM, Schor DS, Wanders RJ, Jakobs C. ten Brink HJ, et al. J Lipid Res. 1992 Jan;33(1):41-7. J Lipid Res. 1992. PMID: 1372637 Free article.

3

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. J Lipid Res. 1992 Oct;33(10):1449-57. J Lipid Res. 1992. PMID: 1385561 Free article.

4

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. J Inherit Metab Dis. 1991;14(5):681-4. doi: 10.1007/BF01799934. J Inherit Metab Dis. 1991. PMID: 1779614

5

The inborn errors of peroxisomal beta-oxidation: a review.

Wanders RJ, van Roermund CW, Schutgens RB, Barth PG, Heymans HS, van den Bosch H, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330. J Inherit Metab Dis. 1990. PMID: 2109148 Review.

6

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

7

Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.

Wanders RJ, van Wijland MJ, van Roermund CW, Schutgens RB, van den Bosch H, Tager JM, Nijenhuis A, Tromp A. Wanders RJ, et al. Clin Chim Acta. 1987 Jun 15;165(2-3):303-10. doi: 10.1016/0009-8981(87)90175-6. Clin Chim Acta. 1987. PMID: 3652452

8

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.

9

Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studies.

Barth PG, Wanders RJ, Schutgens RB, Staalman CR. Barth PG, et al. Am J Med Genet. 1996 Mar 15;62(2):164-8. doi: 10.1002/(SICI)1096-8628(19960315)62:2<164::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8882397

10

Metabolic aspects of peroxisomal disorders.

Wanders RJ, Jansen G, van Roermund CW, Denis S, Schutgens RB, Jakobs BS. Wanders RJ, et al. Ann N Y Acad Sci. 1996 Dec 27;804:450-60. doi: 10.1111/j.1749-6632.1996.tb18636.x. Ann N Y Acad Sci. 1996. PMID: 8993564

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