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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 1835339

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

  • 2. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Jackson S, Bartlett K, Land J, Moxon ER, Pollitt RJ, Leonard JV, Turnbull DM.
    Pediatr Res; 1991 Apr; 29(4 Pt 1):406-11. PubMed ID: 1830138
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease.
    Yang SY, He XY, Schulz H.
    FEBS J; 2005 Oct; 272(19):4874-83. PubMed ID: 16176262
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
    Miyajima H, Orii KE, Shindo Y, Hashimoto T, Shinka T, Kuhara T, Matsumoto I, Shimizu H, Kaneko E.
    Neurology; 1997 Sep; 49(3):833-7. PubMed ID: 9305349
    [Abstract] [Full Text] [Related]

  • 7. Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndrome.
    Fryburg JS, Pelegano JP, Bennett MJ, Bebin EM.
    Am J Med Genet; 1994 Aug 01; 52(1):97-102. PubMed ID: 7977472
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.
    Kamijo T, Wanders RJ, Saudubray JM, Aoyama T, Komiyama A, Hashimoto T.
    J Clin Invest; 1994 Apr 01; 93(4):1740-7. PubMed ID: 8163672
    [Abstract] [Full Text] [Related]

  • 9. Expression and purification of His-tagged rat mitochondrial short-chain 3-hydroxyacyl-CoA dehydrogenase wild-type and Ser137 mutant proteins.
    Liu X, Chu X, Yu W, Li P, Li D.
    Protein Expr Purif; 2004 Oct 01; 37(2):344-51. PubMed ID: 15358356
    [Abstract] [Full Text] [Related]

  • 10. Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Amirkhan RH, Timmons CF, Brown KO, Weinberger MJ, Bennett MJ.
    Arch Pathol Lab Med; 1997 Jul 01; 121(7):730-4. PubMed ID: 9240910
    [Abstract] [Full Text] [Related]

  • 11. Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.
    Treacy EP, Lambert DM, Barnes R, Boriack RL, Vockley J, O'brien LK, Jones PM, Bennett MJ.
    J Pediatr; 2000 Aug 01; 137(2):257-9. PubMed ID: 10931422
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Pons R, Roig M, Riudor E, Ribes A, Briones P, Ortigosa L, Baldellou A, Gil-Gibernau J, Olesti M, Navarro C, Wanders RJ.
    Pediatr Neurol; 1996 Apr 01; 14(3):236-43. PubMed ID: 8736409
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism.
    Barycki JJ, O'Brien LK, Bratt JM, Zhang R, Sanishvili R, Strauss AW, Banaszak LJ.
    Biochemistry; 1999 May 04; 38(18):5786-98. PubMed ID: 10231530
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.