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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. Eur J Pediatr. 1986 Feb;144(5):430-40. doi: 10.1007/BF00441734. Eur J Pediatr. 1986. PMID: 3514227 Review. No abstract available.
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase.
Behbehani AW, Goebel H, Osse G, Gabriel M, Langenbeck U, Berden J, Berger R, Schutgens RB. Behbehani AW, et al. Among authors: schutgens rb. Eur J Pediatr. 1984 Nov;143(1):67-71. doi: 10.1007/BF00442753. Eur J Pediatr. 1984. PMID: 6096151
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: schutgens rb. Eur J Pediatr. 1986 Apr;145(1-2):136-8. doi: 10.1007/BF00441876. Eur J Pediatr. 1986. PMID: 3732317
Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome.
Jakobs C, ten Brink H, Kok RM, Stellaard F, Kleijer WJ, Wanders RJ, Schutgens RB. Jakobs C, et al. Among authors: schutgens rb. Eur J Pediatr. 1989 Apr;148(6):581. doi: 10.1007/BF00441567. Eur J Pediatr. 1989. PMID: 2744027 No abstract available.
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: schutgens rb. Eur J Pediatr. 1986 Aug;145(3):172-5. doi: 10.1007/BF00446057. Eur J Pediatr. 1986. PMID: 2429839
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course.
Barth PG, Wanders RJ, Schutgens RB, Bleeker-Wagemakers EM, van Heemstra D. Barth PG, et al. Among authors: schutgens rb. Eur J Pediatr. 1990 Jul;149(10):722-6. doi: 10.1007/BF01959531. Eur J Pediatr. 1990. PMID: 2209666
Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient.
Santer R, Claviez A, Oldigs HD, Schaub J, Schutgens RB, Wanders RJ. Santer R, et al. Among authors: schutgens rb. Eur J Pediatr. 1993 Apr;152(4):339-42. doi: 10.1007/BF01956749. Eur J Pediatr. 1993. PMID: 8482286
A new type of peroxisomal disorder with variable expression in liver and fibroblasts.
Mandel H, Espeel M, Roels F, Sofer N, Luder A, Iancu TC, Aizin A, Berant M, Wanders RJ, Schutgens RB. Mandel H, et al. Among authors: schutgens rb. J Pediatr. 1994 Oct;125(4):549-55. doi: 10.1016/s0022-3476(94)70006-0. J Pediatr. 1994. PMID: 7931872
Bile acids in peroxisomal disorders.
Van Eldere JR, Parmentier GG, Eyssen HJ, Wanders RJ, Schutgens RB, Vamecq J, Van Hoof F, Poll-The BT, Saudubray JM. Van Eldere JR, et al. Among authors: schutgens rb. Eur J Clin Invest. 1987 Oct;17(5):386-90. doi: 10.1111/j.1365-2362.1987.tb01131.x. Eur J Clin Invest. 1987. PMID: 2446876
Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients.
Theil AC, Schutgens RB, Wanders RJ, Heymans HS. Theil AC, et al. Among authors: schutgens rb. Eur J Pediatr. 1992 Feb;151(2):117-20. doi: 10.1007/BF01958955. Eur J Pediatr. 1992. PMID: 1371465
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