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Page 1
Peroxisomal disorders in neurology.
Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM. Wanders RJ, et al. Among authors: barth pg. 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.
Peroxisomal disorders: a review.
Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. Among authors: barth pg. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 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: barth pg. J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330. J Inherit Metab Dis. 1990. PMID: 2109148 Review.
High incidence of hyperoxaluria in generalized peroxisomal disorders.
van Woerden CS, Groothoff JW, Wijburg FA, Duran M, Wanders RJ, Barth PG, Poll-The BT. van Woerden CS, et al. Among authors: barth pg. Mol Genet Metab. 2006 Aug;88(4):346-50. doi: 10.1016/j.ymgme.2006.03.004. Epub 2006 Apr 18. Mol Genet Metab. 2006. PMID: 16621644
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. J Inherit Metab Dis. 1987;10(3):253-9. doi: 10.1007/BF01800071. J Inherit Metab Dis. 1987. PMID: 3123783
251 results