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A far advanced case of gyrate atrophy in a 12-year-old girl.
Bakker HD, Abeling NG, van Schooneveld MJ, Wanders RJ, van Gennip AH. Bakker HD, et al. Among authors: wanders rj. J Inherit Metab Dis. 1991;14(3):379-81. doi: 10.1007/BF01811708. J Inherit Metab Dis. 1991. PMID: 1770797 No abstract available.
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.
Peroxisomal disorders in neurology.
Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM. Wanders RJ, et al. J Neurol Sci. 1988 Dec;88(1-3):1-39. doi: 10.1016/0022-510x(88)90203-1. J Neurol Sci. 1988. PMID: 3066850 Review.
A sibship with a mild variant of Zellweger syndrome.
Barth PG, Schutgens RB, Wanders RJ, Heymans HS, Moser AE, Moser HW, Bleeker-Wagemakers EM, Jansonius-Schultheiss K, Derix M, Nelck GF. Barth PG, et al. Among authors: wanders rj. J Inherit Metab Dis. 1987;10(3):253-9. doi: 10.1007/BF01800071. J Inherit Metab Dis. 1987. PMID: 3123783
Peroxisomal disorders: a review.
Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 Review.
1,020 results