227 related articles for article (PubMed ID: 3379344)
1. Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.
Schrakamp G; Schalkwijk CG; Schutgens RB; Wanders RJ; Tager JM; van den Bosch H
J Lipid Res; 1988 Mar; 29(3):325-34. PubMed ID: 3379344
[TBL] [Abstract][Full Text] [Related]
2. Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.
van den Bosch H; Schalkwijk CG; Schrakamp G; Wanders RJ; Schutgens RB; Schram AW; Tager JM
Prog Clin Biol Res; 1988; 282():139-50. PubMed ID: 3071794
[TBL] [Abstract][Full Text] [Related]
3. The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts.
Schrakamp G; Schutgens RB; Wanders RJ; Heymans HS; Tager JM; Van den Bosch H
Biochim Biophys Acta; 1985 Jan; 833(1):170-4. PubMed ID: 3967038
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Glyceryl ethers in peroxisomal disease.
Poulos A; Bankier A; Beckman K; Johnson D; Robertson EF; Sharp P; Sheffield L; Singh H; Usher S; Wise G
Clin Genet; 1991 Jan; 39(1):13-25. PubMed ID: 1705185
[TBL] [Abstract][Full Text] [Related]
7. Fatty alcohol accumulation in the autosomal recessive form of rhizomelic chondrodysplasia punctata.
Rizzo WB; Craft DA; Judd LL; Moser HW; Moser AB
Biochem Med Metab Biol; 1993 Aug; 50(1):93-102. PubMed ID: 8373640
[TBL] [Abstract][Full Text] [Related]
8. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
Hoefler G; Hoefler S; Watkins PA; Chen WW; Moser A; Baldwin V; McGillivary B; Charrow J; Friedman JM; Rutledge L
J Pediatr; 1988 May; 112(5):726-33. PubMed ID: 2452243
[TBL] [Abstract][Full Text] [Related]
9. Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
Wanders RJ; Schutgens RB; Schrakamp G; Tager JM; Van den Bosch H; Moser AB; Moser HW
J Neurol Sci; 1987 Feb; 77(2-3):331-40. PubMed ID: 3819771
[TBL] [Abstract][Full Text] [Related]
10. The role of peroxisomes in glycerol ether lipid metabolism.
Hajra AK; Horie S; Webber KO
Prog Clin Biol Res; 1988; 282():99-116. PubMed ID: 3071810
[TBL] [Abstract][Full Text] [Related]
11. Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.
Wanders RJ; van Roermund CW; van Wijland MJ; Heikoop J; Schutgens RB; Schram AW; Tager JM; van den Bosch H; Poll-Thé BT; Saudubray JM
Clin Chim Acta; 1987 Jul; 166(2-3):255-63. PubMed ID: 2441904
[TBL] [Abstract][Full Text] [Related]
12. In vitro and in vivo plasmalogen replacement evaluations in rhizomelic chrondrodysplasia punctata and Pelizaeus-Merzbacher disease using PPI-1011, an ether lipid plasmalogen precursor.
Wood PL; Khan MA; Smith T; Ehrmantraut G; Jin W; Cui W; Braverman NE; Goodenowe DB
Lipids Health Dis; 2011 Oct; 10():182. PubMed ID: 22008564
[TBL] [Abstract][Full Text] [Related]
13. Plasmalogens and fatty alcohols in rhizomelic chondrodysplasia punctata and Sjögren-Larsson syndrome.
Malheiro AR; da Silva TF; Brites P
J Inherit Metab Dis; 2015 Jan; 38(1):111-21. PubMed ID: 25432520
[TBL] [Abstract][Full Text] [Related]
14. Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.
Hoefler G; Paschke E; Hoefler S; Moser AB; Moser HW
J Clin Invest; 1991 Dec; 88(6):1873-9. PubMed ID: 1752949
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Inherited disorders of fatty alcohol metabolism.
Rizzo WB
Mol Genet Metab; 1998 Oct; 65(2):63-73. PubMed ID: 9787098
[TBL] [Abstract][Full Text] [Related]
17. The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.
Roscher A; Molzer B; Bernheimer H; Stöckler S; Mutz I; Paltauf F
Pediatr Res; 1985 Sep; 19(9):930-3. PubMed ID: 4047762
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Cholesterol biosynthesis in dermal fibroblasts from patients with metabolic disorders of peroxisomal origin.
Malle E; Oettl K; Sattler W; Hoefler G; Kostner GM
Eur J Clin Invest; 1995 Jan; 25(1):59-67. PubMed ID: 7705389
[TBL] [Abstract][Full Text] [Related]
20. Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.
Barr DG; Kirk JM; al Howasi M; Wanders RJ; Schutgens RB
Arch Dis Child; 1993 Mar; 68(3):415-7. PubMed ID: 8466247
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
