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2. Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case report. Wanders RJ; Boltshauser E; Steinmann B; Spycher MA; Schutgens RB; van den Bosch H; Tager JM J Neurol Sci; 1990 Aug; 98(1):1-11. PubMed ID: 1700075 [TBL] [Abstract][Full Text] [Related]
3. Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease. Wanders RJ; Heymans HS; Schutgens RB; Poll-Thé BT; Saudubray JM; Tager JM; Schrakamp G; van den Bosch H J Neurol Sci; 1988 Apr; 84(2-3):147-55. PubMed ID: 2454298 [TBL] [Abstract][Full Text] [Related]
4. Infantile Refsum's disease: a peroxisomal storage disorder? Manson JI; Pollard AC; Poulos A; Carter RF Clin Exp Neurol; 1985; 21():283-7. PubMed ID: 2436838 [TBL] [Abstract][Full Text] [Related]
5. Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblasts. Beard ME; Moser AB; Sapirstein V; Holtzman E J Inherit Metab Dis; 1986; 9(4):321-34. PubMed ID: 2435984 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Refsum disease: a defect in the alpha-oxidation of phytanic acid in peroxisomes. Singh I; Pahan K; Singh AK; Barbosa E J Lipid Res; 1993 Oct; 34(10):1755-64. PubMed ID: 7504046 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. The influence of the branched-chain fatty acids pristanic acid and Refsum disease-associated phytanic acid on mitochondrial functions and calcium regulation of hippocampal neurons, astrocytes, and oligodendrocytes. Rönicke S; Kruska N; Kahlert S; Reiser G Neurobiol Dis; 2009 Nov; 36(2):401-10. PubMed ID: 19703563 [TBL] [Abstract][Full Text] [Related]
10. Studies on the degradation of [U-3H]-phytanic acid and [U-3H]-pristanic acid in cultured fibroblasts from children with peroxisomal disorders. Kase BF; Björkhem I Scand J Clin Lab Invest; 1996 May; 56(3):211-7. PubMed ID: 8761525 [TBL] [Abstract][Full Text] [Related]
11. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids. Aubourg P; Kremser K; Roland MO; Rocchiccioli F; Singh I Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868 [TBL] [Abstract][Full Text] [Related]
12. Phytanic acid and pristanic acid, branched-chain fatty acids associated with Refsum disease and other inherited peroxisomal disorders, mediate intracellular Ca2+ signaling through activation of free fatty acid receptor GPR40. Kruska N; Reiser G Neurobiol Dis; 2011 Aug; 43(2):465-72. PubMed ID: 21570468 [TBL] [Abstract][Full Text] [Related]
13. Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years. Robertson EF; Poulos A; Sharp P; Manson J; Wise G; Jaunzems A; Carter R Eur J Pediatr; 1988 Feb; 147(2):133-42. PubMed ID: 2452736 [TBL] [Abstract][Full Text] [Related]
14. Infantile Refsum's disease: a generalized peroxisomal disorder. Case report with postmortem examination. Torvik A; Torp S; Kase BF; Ek J; Skjeldal O; Stokke O J Neurol Sci; 1988 May; 85(1):39-53. PubMed ID: 2455020 [TBL] [Abstract][Full Text] [Related]
16. [Two siblings of Leber's congenital amaurosis with an increase in very long chain fatty acid in blood: relationship between peroxisomal disorders and Leber's congenital amaurosis]. Haginoya K; Aikawa J; Noro T; Watanabe M; Iinuma K; Narisawa K; Tada K No To Hattatsu; 1989 Jul; 21(4):348-53. PubMed ID: 2789858 [TBL] [Abstract][Full Text] [Related]
17. Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution. Baumgartner MR; Jansen GA; Verhoeven NM; Mooyer PA; Jakobs C; Roels F; Espeel M; Fourmaintraux A; Bellet H; Wanders RJ; Saudubray JM Ann Neurol; 2000 Jan; 47(1):109-13. PubMed ID: 10632109 [TBL] [Abstract][Full Text] [Related]
18. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]. Molzer B; Stöckler S; Bernheimer H Wien Klin Wochenschr; 1992; 104(21):665-70. PubMed ID: 1282286 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]