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108 results
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A lethal defect of mitochondrial and peroxisomal fission.
Waterham HR, Koster J, van Roermund CW, Mooyer PA, Wanders RJ, Leonard JV. Waterham HR, et al. Among authors: van roermund cw. N Engl J Med. 2007 Apr 26;356(17):1736-41. doi: 10.1056/NEJMoa064436. N Engl J Med. 2007. PMID: 17460227
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: van roermund cw. Prog Clin Biol Res. 1992;375:507-19. Prog Clin Biol Res. 1992. PMID: 1438395 Review. No abstract available.
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. Among authors: van roermund cw. J Inherit Metab Dis. 1992;15(4):634-44. doi: 10.1007/BF01799620. J Inherit Metab Dis. 1992. PMID: 1528022 Review.
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. Among authors: van roermund cw, van den bosch h. J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330. J Inherit Metab Dis. 1990. PMID: 2109148 Review.
Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.
Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Tager JM, van den Bosch H, Thomas GH. Wanders RJ, et al. Among authors: van roermund cw, van wijland mj, van den bosch h. J Inherit Metab Dis. 1988;11 Suppl 2:161-4. doi: 10.1007/BF01804225. J Inherit Metab Dis. 1988. PMID: 3141699 No abstract available.
X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts.
Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Schram AW, Tager JM, van den Bosch H, Schalkwijk C. Wanders RJ, et al. Among authors: van roermund cw, van wijland mj, van den bosch h. J Inherit Metab Dis. 1988;11 Suppl 2:173-7. doi: 10.1007/BF01804228. J Inherit Metab Dis. 1988. PMID: 3141702 No abstract available.
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. Among authors: van roermund cw, van wijland mj, van den bosch h. 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
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