These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 3289796)

  • 21. Stereological analysis of peroxisomes and mitochondria in intestinal epithelium of patients with peroxisomal deficiency disorders: Zellweger's syndrome and neonatal-onset adrenoleukodystrophy.
    Black VH; Cornacchia L
    Am J Anat; 1986 Sep; 177(1):107-18. PubMed ID: 3776884
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometry.
    Clayton PT; Lake BD; Hall NA; Shortland DB; Carruthers RA; Lawson AM
    Eur J Pediatr; 1987 Mar; 146(2):166-73. PubMed ID: 2436918
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. The peroxisome and the eye.
    Folz SJ; Trobe JD
    Surv Ophthalmol; 1991; 35(5):353-68. PubMed ID: 1710072
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?
    Poulos A; Sharp P; Whiting M
    Clin Genet; 1984 Dec; 26(6):579-86. PubMed ID: 6209040
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Peroxisomes and neurologic diseases].
    Sereni C; Paturneau-Jouas M
    Rev Neurol (Paris); 1989; 145(5):341-9. PubMed ID: 2472665
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Peroxisomal disorders: clinical characterization.
    Monnens L; Heymans H
    J Inherit Metab Dis; 1987; 10 Suppl 1():23-32. PubMed ID: 2446046
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pipecolic acid is oxidized by renal and hepatic peroxisomes. Implications for Zellweger's cerebro-hepato-renal syndrome (CHRS).
    Zaar K; Angermüller S; Völkl A; Fahimi HD
    Exp Cell Res; 1986 May; 164(1):267-71. PubMed ID: 2869967
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. 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]  

  • 39. Prenatal and perinatal diagnosis of peroxisomal disorders.
    Schutgens RB; Schrakamp G; Wanders RJ; Heymans HS; Tager JM; van den Bosch H
    J Inherit Metab Dis; 1989; 12 Suppl 1():118-34. PubMed ID: 2509803
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.