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Journal Abstract Search

140 related items for PubMed ID: 8993562

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.
    Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM.
    J Inherit Metab Dis; 1992; 15(3):385-8. PubMed ID: 1357231
    [No Abstract] [Full Text] [Related]

  • 3. Biochemical findings in a series of Australian patients with isolated defects in peroxisomal beta-oxidation.
    Paton BC, Sharp PC, Poulos A.
    Ann N Y Acad Sci; 1996 Dec 27; 804():750-1. PubMed ID: 8993614
    [No Abstract] [Full Text] [Related]

  • 4. [Peroxisomal disorders].
    Suzuki Y, Shimozawa N, Imamura A, Kondo N.
    Ryoikibetsu Shokogun Shirizu; 2000 Dec 27; (29 Pt 4):452-9. PubMed ID: 11031991
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 6. Peroxisomal bifunctional enzyme deficiency.
    Watkins PA, Chen WW, Harris CJ, Hoefler G, Hoefler S, Blake DC, Balfe A, Kelley RI, Moser AB, Beard ME.
    J Clin Invest; 1989 Mar 27; 83(3):771-7. PubMed ID: 2921319
    [Abstract] [Full Text] [Related]

  • 7. D-hydroxyacyl-CoA dehydrogenase deficiency. Identification of a new peroxisomal disorder with implications for other disorders of beta-oxidation.
    van Grunsven EG, van Berkel E, Denis S, Mooijer PA, Wanders RJ.
    Adv Exp Med Biol; 1999 Mar 27; 466():365-9. PubMed ID: 10709664
    [Abstract] [Full Text] [Related]

  • 8. A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities.
    Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Tager JM, Stephenson JB, Clayton PT.
    J Inherit Metab Dis; 1990 Mar 27; 13(3):375-9. PubMed ID: 2122104
    [No Abstract] [Full Text] [Related]

  • 9. Peroxisomal bifunctional enzyme complex deficiency with associated retinal findings.
    Eustis HS, Curry T, Superneau DW.
    J Pediatr Ophthalmol Strabismus; 1995 Mar 27; 32(2):125-7. PubMed ID: 7629669
    [Abstract] [Full Text] [Related]

  • 10. Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein.
    van Grunsven EG, van Roermund CW, Denis S, Wanders RJ.
    Biochem Biophys Res Commun; 1997 Jun 09; 235(1):176-9. PubMed ID: 9196058
    [Abstract] [Full Text] [Related]

  • 11. [Peroxisomal disorders--clinical and biochemical studies].
    Shimozawa N, Suzuki Y, Yamaguchi S, Shimizu N, Orii T.
    No To Hattatsu; 1988 Nov 09; 20(6):480-91. PubMed ID: 3242571
    [No Abstract] [Full Text] [Related]

  • 12. Peroxisomal bifunctional enzyme deficiency with associated retinal findings.
    Al-Hazzaa SA, Ozand PT.
    Ophthalmic Genet; 1997 Jun 09; 18(2):93-9. PubMed ID: 9228246
    [Abstract] [Full Text] [Related]

  • 13. Peroxisomal beta-oxidation: enzymology and molecular biology.
    Hashimoto T.
    Ann N Y Acad Sci; 1996 Dec 27; 804():86-98. PubMed ID: 8993538
    [No Abstract] [Full Text] [Related]

  • 14. Clinical consequences of defects in peroxisomal beta-oxidation.
    Clayton PT.
    Biochem Soc Trans; 2001 May 27; 29(Pt 2):298-305. PubMed ID: 11356171
    [Abstract] [Full Text] [Related]

  • 15. Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.
    Kaufmann WE, Theda C, Naidu S, Watkins PA, Moser AB, Moser HW.
    Ann Neurol; 1996 Feb 27; 39(2):268-71. PubMed ID: 8967760
    [Abstract] [Full Text] [Related]

  • 16. [Bifunctional enzyme deficiency].
    Suzuki Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb 27; (19 Pt 2):326-7. PubMed ID: 9645073
    [No Abstract] [Full Text] [Related]

  • 17. Investigation of peroxisomal lipid beta-oxidation enzymes in guinea pig liver peroxisomes by immunoblotting and immunocytochemistry.
    Yamamoto K, Völkl A, Fahimi HD.
    J Histochem Cytochem; 1992 Dec 27; 40(12):1909-18. PubMed ID: 1360481
    [Abstract] [Full Text] [Related]

  • 18.
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    [No Abstract] [Full Text] [Related]

  • 19. Transcription regulation of peroxisomal fatty acyl-CoA oxidase and enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase in rat liver by peroxisome proliferators.
    Reddy JK, Goel SK, Nemali MR, Carrino JJ, Laffler TG, Reddy MK, Sperbeck SJ, Osumi T, Hashimoto T, Lalwani ND.
    Proc Natl Acad Sci U S A; 1986 Mar 27; 83(6):1747-51. PubMed ID: 3456610
    [Abstract] [Full Text] [Related]

  • 20. Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basis.
    Van Grunsven EG, van Berkel E, Lemonde H, Clayton PT, Wanders RJ.
    J Inherit Metab Dis; 1998 Jun 27; 21(3):298-301. PubMed ID: 9686380
    [No Abstract] [Full Text] [Related]

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