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6. Fatty acid composition of tissues in Refsum's disease (herodopathia atactica polyneuritiformis). Estimation of total phytanic acid accumulation. Malmendier CL; Jonniaux G; Voet W; Van Den Bergen CJ Biomedicine; 1974 Nov; 20(6):398-407. PubMed ID: 4141904 [No Abstract] [Full Text] [Related]
7. Disorders related to the metabolism of phytanic acid. Stokke O; Skjeldal OH; Høie K Scand J Clin Lab Invest Suppl; 1986; 184():3-10. PubMed ID: 2438746 [TBL] [Abstract][Full Text] [Related]
8. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders. Poll-The BT; Skjeldal OH; Stokke O; Poulos A; Demaugre F; Saudubray JM Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial oxidation of phytanic acid in human and monkey liver: implication that Refsum's disease is not a peroxisomal disorder. Watkins PA; Mihalik SJ Biochem Biophys Res Commun; 1990 Mar; 167(2):580-6. PubMed ID: 1690986 [TBL] [Abstract][Full Text] [Related]
10. Evidence against alpha-hydroxyphytanic acid as an intermediate in the metabolism of phytanic acid. Skjeldal OH; Stokke O Scand J Clin Lab Invest; 1988 Feb; 48(1):97-102. PubMed ID: 2464193 [TBL] [Abstract][Full Text] [Related]
11. Clinical and biochemical heterogeneity in conditions with phytanic acid accumulation. Skjeldal OH; Stokke O; Refsum S; Norseth J; Petit H J Neurol Sci; 1987 Jan; 77(1):87-96. PubMed ID: 2433405 [TBL] [Abstract][Full Text] [Related]
13. Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver. Scotto JM; Hadchouel M; Odievre M; Laudat MH; Saudubray JM; Dulac O; Beucler I; Beaune P J Inherit Metab Dis; 1982; 5(2):83-90. PubMed ID: 6188882 [TBL] [Abstract][Full Text] [Related]
14. Tissue distribution of phytanic acid and its analogues in a kinship with Refsum's disease. Yao JK; Dyck PJ Lipids; 1987 Feb; 22(2):69-75. PubMed ID: 2436023 [TBL] [Abstract][Full Text] [Related]
15. 3-Methyladipate excretion in animals fed a phytol supplement with reference to Refsum's disease. Krywawych S; Brenton DP; Jackson MJ; Forte C; Walker DK; Lawson AM J Inherit Metab Dis; 1985; 8 Suppl 2():147-8. PubMed ID: 2413274 [No Abstract] [Full Text] [Related]
17. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders. Molzer B; Kainz-Korschinsky M; Sundt-Heller R; Bernheimer H J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624 [TBL] [Abstract][Full Text] [Related]
18. Peroxisomes, Refsum's disease and the alpha- and omega-oxidation of phytanic acid. Wanders RJ; Komen JC Biochem Soc Trans; 2007 Nov; 35(Pt 5):865-9. PubMed ID: 17956234 [TBL] [Abstract][Full Text] [Related]
19. Heredopathia atactica polyneurotiformis: therapeutic and pathogenetic aspects. Refsum S Riv Patol Nerv Ment; 1976 Jun; 97(3):115-26. PubMed ID: 74082 [TBL] [Abstract][Full Text] [Related]
20. CYP4 isoform specificity in the omega-hydroxylation of phytanic acid, a potential route to elimination of the causative agent of Refsum's disease. Xu F; Ng VY; Kroetz DL; de Montellano PR J Pharmacol Exp Ther; 2006 Aug; 318(2):835-9. PubMed ID: 16707724 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]