139 related articles for article (PubMed ID: 1636502)
1. Severe changes in polyunsaturated fatty acids in the brain, liver, kidney, and retina in patients with peroxisomal disorders.
Martinez M
Adv Exp Med Biol; 1992; 318():347-59. PubMed ID: 1636502
[No Abstract] [Full Text] [Related]
2. Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders.
Martinez M
Brain Res; 1992 Jun; 583(1-2):171-82. PubMed ID: 1504825
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Very long-chain fatty acids in peroxisomal disease.
Poulos A; Beckman K; Johnson DW; Paton BC; Robinson BS; Sharp P; Usher S; Singh H
Adv Exp Med Biol; 1992; 318():331-40. PubMed ID: 1378993
[TBL] [Abstract][Full Text] [Related]
5. Polyunsaturated fatty acids in the developing human brain, red cells and plasma: influence of nutrition and peroxisomal disease.
Martinez M
World Rev Nutr Diet; 1994; 75():70-8. PubMed ID: 7871835
[No Abstract] [Full Text] [Related]
6. Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation.
Clayton PT; Lake BD; Hjelm M; Stephenson JB; Besley GT; Wanders RJ; Schram AW; Tager JM; Schutgens RB; Lawson AM
J Inherit Metab Dis; 1988; 11 Suppl 2():165-8. PubMed ID: 3141700
[No Abstract] [Full Text] [Related]
7. Peroxisomal diseases.
Goldfischer SL
Prog Clin Biol Res; 1988; 282():117-37. PubMed ID: 3071793
[No Abstract] [Full Text] [Related]
8. 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
Eur J Clin Invest; 1987 Oct; 17(5):386-90. PubMed ID: 2446876
[TBL] [Abstract][Full Text] [Related]
9. Metabolism of branched chain fatty acids in peroxisomal disorders.
Singh H; Usher S; Johnson D; Poulos A
J Inherit Metab Dis; 1990; 13(3):387-9. PubMed ID: 1700192
[No Abstract] [Full Text] [Related]
10. Severe deficiency of docosahexaenoic acid in peroxisomal disorders: a defect of delta 4 desaturation?
Martínez M
Neurology; 1990 Aug; 40(8):1292-8. PubMed ID: 2143272
[TBL] [Abstract][Full Text] [Related]
11. The peroxisomal disorders.
Moser HW; Goldfischer SL
Hosp Pract (Off Ed); 1985 Sep; 20(9):61-70. PubMed ID: 3928646
[No Abstract] [Full Text] [Related]
12. Essential fatty acids and serine as plasmalogen precursors in relation to competing metabolic pathways.
Cook HW; Thomas SE; Xu Z
Biochem Cell Biol; 1991 Jul; 69(7):475-84. PubMed ID: 1793558
[TBL] [Abstract][Full Text] [Related]
13. A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblasts.
Schutgens RB; Wanders RJ; Jakobs C; Arslan-Kirchner M; Miller K; Wieacker P; Hunnemann D; Hurter P; von Schutz M
J Inherit Metab Dis; 1994; 17(3):319-22. PubMed ID: 7807942
[No Abstract] [Full Text] [Related]
14. Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome.
Martinez M
Lipids; 1989 Apr; 24(4):261-5. PubMed ID: 2755305
[TBL] [Abstract][Full Text] [Related]
15. Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain.
Sharp P; Johnson D; Poulos A
J Neurochem; 1991 Jan; 56(1):30-7. PubMed ID: 1702833
[TBL] [Abstract][Full Text] [Related]
16. Ratios for very-long-chain fatty acids in plasma of subjects with peroxisomal disorders, as determined by HPLC and validated by gas chromatography-mass spectrometry.
Hall NA; Lynes GW; Hjelm NM
Clin Chem; 1988 Jun; 34(6):1041-5. PubMed ID: 2454167
[TBL] [Abstract][Full Text] [Related]
17. Peroxisomal disorders.
Moser HW; Bergin A; Cornblath D
Biochem Cell Biol; 1991 Jul; 69(7):463-74. PubMed ID: 1724376
[TBL] [Abstract][Full Text] [Related]
18. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
Abe Y; Honsho M; Nakanishi H; Taguchi R; Fujiki Y
Biochim Biophys Acta; 2014 Apr; 1841(4):610-9. PubMed ID: 24418004
[TBL] [Abstract][Full Text] [Related]
19. Regulation of the metabolism of polyunsaturated fatty acids.
Hagve TA; Christensen E; Grønn M; Christophersen BO
Scand J Clin Lab Invest Suppl; 1988; 191():33-46. PubMed ID: 3073521
[TBL] [Abstract][Full Text] [Related]
20. [Peroxisomal disorders; newer concept and recent studies].
Kamoshita S
Nihon Rinsho; 1990 Mar; 48(3):629-38. PubMed ID: 2192101
[No Abstract] [Full Text] [Related]
[Next] [New Search]