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Peroxisomal disorders: a newly recognised group of genetic diseases.
Schutgens RB, Heymans HS, Wanders RJ, van den Bosch H, Tager JM. Schutgens RB, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Feb;144(5):430-40. doi: 10.1007/BF00441734. Eur J Pediatr. 1986. PMID: 3514227 Review. No abstract available.
Impaired plasmalogen metabolism in infantile Refsum's disease.
Poll-Thé BT, Ogier H, Saudubray JM, Schutgens RB, Wanders RJ, van den Bosch H, Schrakamp G. Poll-Thé BT, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Feb;144(5):513-4. doi: 10.1007/BF00441753. Eur J Pediatr. 1986. PMID: 2420599 No abstract available.
A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells.
Wanders RJ, Schrakamp G, van den Bosch H, Tager JM, Schutgens RB. Wanders RJ, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Apr;145(1-2):136-8. doi: 10.1007/BF00441876. Eur J Pediatr. 1986. PMID: 3732317
Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins.
Wanders RJ, Schutgens RB, Schrakamp G, van den Bosch H, Tager JM, Schram AW, Hashimoto T, Poll-Thé BT, Saudubrau JM. Wanders RJ, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Aug;145(3):172-5. doi: 10.1007/BF00446057. Eur J Pediatr. 1986. PMID: 2429839
Prenatal and perinatal diagnosis of peroxisomal disorders.
Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H. Schutgens RB, et al. Among authors: van den bosch h. J Inherit Metab Dis. 1989;12 Suppl 1:118-34. doi: 10.1007/BF01799291. J Inherit Metab Dis. 1989. PMID: 2509803 Review.
Peroxisomal disorders in neurology.
Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM. Wanders RJ, et al. Among authors: van den bosch h. 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.
Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
van den Bosch H, Schalkwijk CG, Schrakamp G, Wanders RJ, Schutgens RB, Schram AW, Tager JM. van den Bosch H, et al. Prog Clin Biol Res. 1988;282:139-50. Prog Clin Biol Res. 1988. PMID: 3071794 Review.
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.
Schrakamp G, Schalkwijk CG, Schutgens RB, Wanders RJ, Tager JM, van den Bosch H. Schrakamp G, et al. Among authors: van den bosch h. J Lipid Res. 1988 Mar;29(3):325-34. J Lipid Res. 1988. PMID: 3379344
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.
Genetic relation between the Zellweger syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata.
Wanders RJ, Saelman D, Heymans HS, Schutgens RB, Westerveld A, Poll-Thé BT, Saudubray JM, Van den Bosch H, Strijland A, Schram AW, et al. Wanders RJ, et al. Among authors: van den bosch h. N Engl J Med. 1986 Mar 20;314(12):787-8. doi: 10.1056/NEJM198603203141216. N Engl J Med. 1986. PMID: 2419755 No abstract available.
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