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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: heymans hs. 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.
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders.
Brul S, Wiemer EA, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, Van den Bosch H, Tager JM. Brul S, et al. Among authors: heymans hs. Biochem Biophys Res Commun. 1988 May 16;152(3):1083-9. doi: 10.1016/s0006-291x(88)80395-4. Biochem Biophys Res Commun. 1988. PMID: 3377768
Peroxisomal dysfunction in chondrodysplasia punctata, rhizomelic type.
Oorthuys JW, Loewer-Sieger DH, Schutgens RB, Wanders RJ, Heymans HS, Bleeker-Wagemakers EM. Oorthuys JW, et al. Among authors: heymans hs. Ophthalmic Paediatr Genet. 1987 Nov;8(3):183-5. doi: 10.3109/13816818709031467. Ophthalmic Paediatr Genet. 1987. PMID: 3438058
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: heymans hs. J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330. J Inherit Metab Dis. 1990. PMID: 2109148 Review.
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
Brul S, Westerveld A, Strijland A, Wanders RJ, Schram AW, Heymans HS, Schutgens RB, van den Bosch H, Tager JM. Brul S, et al. Among authors: heymans hs. J Clin Invest. 1988 Jun;81(6):1710-5. doi: 10.1172/JCI113510. J Clin Invest. 1988. PMID: 2454948 Free PMC article.
208 results