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8. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. Tager JM; Brul S; Wiemer EA; Strijland A; Van Driel R; Schutgens RB; Van den Bosch H; Wanders RJ; Westerveld A Prog Clin Biol Res; 1990; 321():545-58. PubMed ID: 2183242 [TBL] [Abstract][Full Text] [Related]
9. [Peroxisomal diseases--a survey]. Theron JJ; van Papendorp DH S Afr Med J; 1996 Jun; 86(6):685-90. PubMed ID: 8764428 [TBL] [Abstract][Full Text] [Related]
10. Human peroxisomal disorders. Depreter M; Espeel M; Roels F Microsc Res Tech; 2003 Jun; 61(2):203-23. PubMed ID: 12740827 [TBL] [Abstract][Full Text] [Related]
11. Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies. Schutgens RB; Wanders RJ; Nijenhuis A; van den Hoek CM; Heymans HS; Schrakamp G; Bleeker-Wagemakers EM; Delleman JW; Schram AW; Tager JM Enzyme; 1987; 38(1-4):161-76. PubMed ID: 3440444 [TBL] [Abstract][Full Text] [Related]
15. Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders. Brosius U; Gärtner J Cell Mol Life Sci; 2002 Jun; 59(6):1058-69. PubMed ID: 12169017 [TBL] [Abstract][Full Text] [Related]
16. [The diagnosis of peroxisomal disorders in Spain during the period 1987-1997]. Girós M; Ruiz M; Ribes A; Pàmpols T Rev Neurol; 1999 Jan; 28 Suppl 1():S40-4. PubMed ID: 10778487 [TBL] [Abstract][Full Text] [Related]
17. [Peroxisomal diseases--oxygen and free radicals]. Kremser K; Kovacs W; Stangl H Wien Klin Wochenschr; 1995; 107(22):690-3. PubMed ID: 8533430 [TBL] [Abstract][Full Text] [Related]
18. 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 J Clin Invest; 1988 Jun; 81(6):1710-5. PubMed ID: 2454948 [TBL] [Abstract][Full Text] [Related]
19. Straight-chain acyl-CoA oxidase knockout mouse accumulates extremely long chain fatty acids from alpha-linolenic acid: evidence for runaway carousel-type enzyme kinetics in peroxisomal beta-oxidation diseases. Infante JP; Tschanz CL; Shaw N; Michaud AL; Lawrence P; Brenna JT Mol Genet Metab; 2002 Feb; 75(2):108-19. PubMed ID: 11855929 [TBL] [Abstract][Full Text] [Related]
20. Prenatal and perinatal diagnosis of peroxisomal disorders. Schutgens RB; Schrakamp G; Wanders RJ; Heymans HS; Tager JM; van den Bosch H J Inherit Metab Dis; 1989; 12 Suppl 1():118-34. PubMed ID: 2509803 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]