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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: schutgens rb. J Inherit Metab Dis. 1992;15(4):634-44. doi: 10.1007/BF01799620. J Inherit Metab Dis. 1992. PMID: 1528022 Review.
Zellweger syndrome in a preterm, small for gestational age infant.
Samsom JF, Jakobs C, van de Klei-van Moorsel J, Smit LM, Schutgens RB, Wanders RJ. Samsom JF, et al. Among authors: schutgens rb. J Inherit Metab Dis. 1992;15(1):75-83. doi: 10.1007/BF01800347. J Inherit Metab Dis. 1992. PMID: 1583879
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: schutgens rb. 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: schutgens rb. J Inherit Metab Dis. 1988;11 Suppl 2:161-4. doi: 10.1007/BF01804225. J Inherit Metab Dis. 1988. PMID: 3141699 No abstract available.
Peroxisomal functions in mulibrey nanism.
Schutgens RB, Ryynänen M, Wanders RJ. Schutgens RB, et al. J Inherit Metab Dis. 1994;17(5):626. doi: 10.1007/BF00711603. J Inherit Metab Dis. 1994. PMID: 7837772 No abstract available.
205 results