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 *

229 related articles for article (PubMed ID: 2420940)

  • 1. Neonatal adrenoleukodystrophy.
    Aubourg P; Scotto J; Rocchiccioli F; Feldmann-Pautrat D; Robain O
    J Neurol Neurosurg Psychiatry; 1986 Jan; 49(1):77-86. PubMed ID: 2420940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.
    Poll-The BT; Saudubray JM; Ogier HA; Odièvre M; Scotto JM; Monnens L; Govaerts LC; Roels F; Cornelis A; Schutgens RB
    Eur J Pediatr; 1987 Sep; 146(5):477-83. PubMed ID: 2445576
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: plasma changes and skin fibroblast phytanic acid oxidase.
    Poulos A; Sharp P; Fellenberg AJ; Danks DM
    Hum Genet; 1985; 70(2):172-7. PubMed ID: 2408988
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. [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]  

  • 6. Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders.
    Hughes JL; Poulos A; Robertson E; Chow CW; Sheffield LJ; Christodoulou J; Carter RF
    Virchows Arch A Pathol Anat Histopathol; 1990; 416(3):255-64. PubMed ID: 1689088
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.
    Aubourg P; Robain O; Rocchiccioli F; Dancea S; Scotto J
    J Neurol Sci; 1985; 69(1-2):9-25. PubMed ID: 4009207
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy.
    Small GM; Santos MJ; Imanaka T; Poulos A; Danks DM; Moser HW; Lazarow PB
    J Inherit Metab Dis; 1988; 11(4):358-71. PubMed ID: 2468817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Adrenoleukodystrophy with olivopontocerebellar atrophy-like lesions.
    Tateishi J; Sato Y; Suetsugu M; Takashiba T
    Clin Neuropathol; 1986; 5(1):34-9. PubMed ID: 3948452
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy).
    Kerckaert I; Dingemans KP; Heymans HS; Vamecq J; Roels F
    J Inherit Metab Dis; 1988; 11(4):372-86. PubMed ID: 2468818
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy.
    Mito T; Takada K; Akaboshi S; Takashima S; Takeshita K; Origuchi Y
    Acta Neuropathol; 1989; 77(4):437-40. PubMed ID: 2540612
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complementation analysis of peroxisomal disorders and classical Refsum.
    Poll-The BT; Skjeldal OH; Stokke O; Demaugre F; Saudubray JM
    Prog Clin Biol Res; 1990; 321():537-43. PubMed ID: 1691507
    [No Abstract]   [Full Text] [Related]  

  • 17. Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.
    Kelley RI; Datta NS; Dobyns WB; Hajra AK; Moser AB; Noetzel MJ; Zackai EH; Moser HW
    Am J Med Genet; 1986 Apr; 23(4):869-901. PubMed ID: 3515938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. In situ genetic complementation analysis of cells with generalized peroxisomal dysfunction.
    Singh AK; Kulvatunyou N; Singh I; Stanley WS
    Hum Hered; 1989; 39(5):298-301. PubMed ID: 2482247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.