BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 2628705)

  • 1. Zellweger syndrome, retinal involvement.
    Stanesu-Segal B; Evrard P
    Metab Pediatr Syst Ophthalmol (1985); 1989; 12(4):96-9. PubMed ID: 2628705
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Retinopathy in Zellweger's cerebrohepatorenal syndrome. The electrophysiological aspects].
    Stănescu-Segall B
    Oftalmologia; 1996; 40(4):357-60. PubMed ID: 8962865
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction.
    Poll-The BT; Saudubray JM; Ogier H; Schutgens RB; Wanders RJ; Schrakamp G; van den Bosch H; Trijbels JM; Poulos A; Moser HW
    J Inherit Metab Dis; 1986; 9(2):169-74. PubMed ID: 2427795
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.
    Kelley RI; Moser HW
    Am J Med Genet; 1984 Dec; 19(4):791-5. PubMed ID: 6517102
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children.
    Budden SS; Kennaway NG; Buist NR; Poulos A; Weleber RG
    J Pediatr; 1986 Jan; 108(1):33-9. PubMed ID: 2418187
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oral bile acid treatment and the patient with Zellweger syndrome.
    Setchell KD; Bragetti P; Zimmer-Nechemias L; Daugherty C; Pelli MA; Vaccaro R; Gentili G; Distrutti E; Dozzini G; Morelli A
    Hepatology; 1992 Feb; 15(2):198-207. PubMed ID: 1735522
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Liver pathologies due to peroxisome disorders].
    Lovisetto P; Raviolo P
    Recenti Prog Med; 1994 Feb; 85(2):134-41. PubMed ID: 8184191
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
    Roscher AA; Hoefler S; Hoefler G; Paschke E; Paltauf F; Moser A; Moser H
    Pediatr Res; 1989 Jul; 26(1):67-72. PubMed ID: 2475849
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients.
    Mihalik SJ; Moser HW; Watkins PA; Danks DM; Poulos A; Rhead WJ
    Pediatr Res; 1989 May; 25(5):548-52. PubMed ID: 2717271
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
    Wilson GN; Holmes RG; Custer J; Lipkowitz JL; Stover J; Datta N; Hajra A
    Am J Med Genet; 1986 May; 24(1):69-82. PubMed ID: 3706414
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Zellweger syndrome: report of one case.
    Lee HF; Mak SC; Wu FW; Chi CS; Huang SC
    Acta Paediatr Taiwan; 2001; 42(1):53-6. PubMed ID: 11270189
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Cerebro-hepato-renal syndrome of Zellweger: clinical symptoms and relevant laboratory findings in 16 patients.
    Govaerts L; Monnens L; Tegelaers W; Trijbels F; van Raay-Selten A
    Eur J Pediatr; 1982 Oct; 139(2):125-8. PubMed ID: 7151832
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome.
    Arneson DW; Tipton RE; Ward JC
    Arch Neurol; 1982 Nov; 39(11):713-6. PubMed ID: 6812554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Importance of peroxisomes in the formation of chenodeoxycholic acid in human liver. Metabolism of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid in Zellweger syndrome.
    Kase BF; Pedersen JI; Wathne KO; Gustafsson J; Björkhem I
    Pediatr Res; 1991 Jan; 29(1):64-9. PubMed ID: 2000261
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Normal fundus and abnormal electroretinogram: differential diagnosis].
    Niemeyer G; Schaefer A
    Klin Monbl Augenheilkd; 2002 Apr; 219(4):259-63. PubMed ID: 12022013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.