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5. Analysis of very long-chain fatty acids and plasmalogen in the erythrocyte membrane: a simple method for the detection of peroxisomal disorders and discrimination between adrenoleukodystrophy and Zellweger syndrome. Tanaka K; Nishizawa K; Yamamoto H; Naruto T; Izeki E; Taga T; Shimada M; Saeki Y Neuropediatrics; 1990 Aug; 21(3):119-23. PubMed ID: 2234315 [TBL] [Abstract][Full Text] [Related]
7. Two siblings with phenotypes mimicking peroxisomal disorders but with discordant biochemical findings. Pietrzyk JJ; Turowska-Heydel D; Klimek M; Kaczmarski F; Kaluza J Clin Pediatr (Phila); 1990 Aug; 29(8):479-84. PubMed ID: 2208910 [TBL] [Abstract][Full Text] [Related]
8. Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects. Paton BC; Sharp PC; Crane DI; Poulos A J Clin Invest; 1996 Feb; 97(3):681-8. PubMed ID: 8609223 [TBL] [Abstract][Full Text] [Related]
10. An improved method for quantification of very long chain fatty acids in plasma. Vallance H; Applegarth D Clin Biochem; 1994 Jun; 27(3):183-6. PubMed ID: 7522996 [TBL] [Abstract][Full Text] [Related]
11. Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders. Kremser K; Roscher A J Clin Chem Clin Biochem; 1989 May; 27(5):315-7. PubMed ID: 2760566 [TBL] [Abstract][Full Text] [Related]
12. [Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?]. Schmitt K; Molzer B; Stöckler S; Tulzer G; Tulzer W Wien Klin Wochenschr; 1993; 105(11):320-2. PubMed ID: 7687405 [TBL] [Abstract][Full Text] [Related]
14. Peroxisomal disorders: clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families. Steinberg SJ; Elçioglu N; Slade CM; Sankaralingam A; Dennis N; Mohammed SN; Fensom AH Am J Med Genet; 1999 Aug; 85(5):502-10. PubMed ID: 10405451 [TBL] [Abstract][Full Text] [Related]
15. Peroxisomal disorders: clinical commentary and future prospects. Wilson GN; Holmes RD; Hajra AK Am J Med Genet; 1988 Jul; 30(3):771-92. PubMed ID: 2461077 [TBL] [Abstract][Full Text] [Related]
16. Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes. Poulos A; Sharp P; Johnson D Neurology; 1989 Jan; 39(1):44-7. PubMed ID: 2462697 [TBL] [Abstract][Full Text] [Related]
17. Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes. Kelley RI; Datta NS; Dobyns WB; Hajra AK; Moser AB; Noetzel MJ; Zackai EH; Moser HW Am J Med Genet; 1986 Apr; 23(4):869-901. PubMed ID: 3515938 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of inborn errors in peroxisomal beta-oxidation. Wanders RJ; Schutgens RB; van den Bosch H; Tager JM; Kleijer WJ Prenat Diagn; 1991 Apr; 11(4):253-61. PubMed ID: 1896411 [TBL] [Abstract][Full Text] [Related]
19. [Liver pathologies due to peroxisome disorders]. Lovisetto P; Raviolo P Recenti Prog Med; 1994 Feb; 85(2):134-41. PubMed ID: 8184191 [TBL] [Abstract][Full Text] [Related]
20. Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls. Moser AB; Kreiter N; Bezman L; Lu S; Raymond GV; Naidu S; Moser HW Ann Neurol; 1999 Jan; 45(1):100-10. PubMed ID: 9894883 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]