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Journal Abstract Search

79 related items for PubMed ID: 13987252

  • 21. Metabolic syndromes with dermatologic manifestations.
    Irons M, Levy HL.
    Clin Rev Allergy; 1986 Feb; 4(1):101-24. PubMed ID: 3516355
    [No Abstract] [Full Text] [Related]

  • 22. ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease.
    Wu JY, Kao HJ, Li SC, Stevens R, Hillman S, Millington D, Chen YT.
    J Clin Invest; 2004 Feb; 113(3):434-40. PubMed ID: 14755340
    [Abstract] [Full Text] [Related]

  • 23. Rapid determination of amino acids in neonatal blood samples based on derivatization with isobutyl chloroformate followed by solid-phase microextraction and gas chromatography/mass spectrometry.
    Deng C, Li N, Zhang X.
    Rapid Commun Mass Spectrom; 2004 Feb; 18(21):2558-64. PubMed ID: 15468143
    [Abstract] [Full Text] [Related]

  • 24. [Phenylketonuria and maple syrup urine disease].
    Bremer HJ.
    Agnes Karll Schwest Krankenpfleger; 1965 Nov; 19(11):427-8. PubMed ID: 5174189
    [No Abstract] [Full Text] [Related]

  • 25. Disorders of amino acid metabolism. Recent advances.
    Clin Pediatr (Phila); 1965 Dec; 4(12):721-31. PubMed ID: 5845405
    [No Abstract] [Full Text] [Related]

  • 26. Maple syrup urine disease: diffusion MRI, and proton MR spectroscopy findings.
    Sener RN.
    Comput Med Imaging Graph; 2007 Mar; 31(2):106-10. PubMed ID: 17207604
    [Abstract] [Full Text] [Related]

  • 27. [Effects of injections of different substrates and an enzyme inhibitor on pigmentation in normal and albino Locusta migratoria L. (Orthop.)].
    Fuzeau-Braesch S.
    C R Seances Soc Biol Fil; 1974 Mar; 168(10-11-12):1226-9. PubMed ID: 4283077
    [No Abstract] [Full Text] [Related]

  • 28. Effect of the branched-chain alpha-keto acids accumulating in maple syrup urine disease on S100B release from glial cells.
    Funchal C, Tramontina F, Quincozes dos Santos A, Fraga de Souza D, Gonçalves CA, Pessoa-Pureur R, Wajner M.
    J Neurol Sci; 2007 Sep 15; 260(1-2):87-94. PubMed ID: 17499767
    [Abstract] [Full Text] [Related]

  • 29. Simultaneous determination of urinary creatinine and UV-absorbing amino acids using a novel low-capacity cation-exchange chromatography for the screening of inborn errors of metabolism.
    Yokoyama Y, Yamasaki K, Sato H.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Feb 25; 816(1-2):333-8. PubMed ID: 15664367
    [Abstract] [Full Text] [Related]

  • 30. Maple syrup urine disease in Thai infants.
    Pangkanon S, Charoensiriwatana W, Sangtawesin V.
    J Med Assoc Thai; 2008 Oct 25; 91 Suppl 3():S41-4. PubMed ID: 19255991
    [Abstract] [Full Text] [Related]

  • 31. THE PREVENTION OF CEREBRAL LESIONS DUE TO ENZYMOPATHIES.
    BICKEL H.
    Bibl Paediatr; 1963 Oct 25; 81():63-75. PubMed ID: 14062996
    [No Abstract] [Full Text] [Related]

  • 32. [Familial amino acid metabolic disorders (alkaptonuria, phenylpyruvic oligophrenia. congenital cataract in the same family)].
    BABEL J, BAMATTER F, COURVOISIER B, FRANCESCHETTI A, KLEIN D, LAPINE A.
    Schweiz Med Wochenschr; 1960 Aug 13; 90():863-6. PubMed ID: 13685529
    [No Abstract] [Full Text] [Related]

  • 33. Posttraumatic dental implant placement in a patient with maple syrup urine disease.
    Oelgiesser D, Levin L, Elpeleg O, Schwartz-Arad D.
    Implant Dent; 2006 Jun 13; 15(2):143-7. PubMed ID: 16766896
    [Abstract] [Full Text] [Related]

  • 34. [Protein metabolism in surgical patients. II. Variations of aminoacidemia and aminoaciduria; chromatographical study].
    PALOMBA R, MERCALLI A.
    G Ital Chir; 1955 May 13; 11(5):440-59. PubMed ID: 14391712
    [No Abstract] [Full Text] [Related]

  • 35. Intrahippocampal administration of the branched-chain alpha-hydroxy acids accumulating in maple syrup urine disease compromises rat performance in aversive and non-aversive behavioral tasks.
    Vasques Vde C, Brinco F, Wajner M.
    J Neurol Sci; 2005 May 15; 232(1-2):11-21. PubMed ID: 15850577
    [Abstract] [Full Text] [Related]

  • 36. [Demographic characteristics and genetics in a small Savoy village (consanguinity, multiple hereditary diseases)].
    DODINVAL P, KLEIN D.
    J Genet Hum; 1962 Mar 15; 11():1-15. PubMed ID: 14028308
    [No Abstract] [Full Text] [Related]

  • 37. INBORN ERRORS OF METABOLISM.
    BEVERIDGE J.
    Bull Postgrad Comm Med Univ Syd; 1963 Sep 15; 19():152-64. PubMed ID: 14052970
    [No Abstract] [Full Text] [Related]

  • 38. Urinary metabolic studies in hereditary macular degeneration.
    Holmgren G, Nordström S, Thorburn W.
    Acta Ophthalmol (Copenh); 1974 Sep 15; 52(2):225-30. PubMed ID: 4406782
    [No Abstract] [Full Text] [Related]

  • 39. [Monodimensional electrophoretic picture of the most frequent hyperaminoacidurias caused by disorders of the intermediate metabolism of aminoacids (pre-renal)].
    Berio A.
    Minerva Pediatr; 1984 Sep 15; 36(17):791-6. PubMed ID: 6521698
    [No Abstract] [Full Text] [Related]

  • 40. [A girl with Lowe's syndrome].
    SCHOLTEN HG.
    Maandschr Kindergeneeskd; 1960 Jul 15; 28():251-5. PubMed ID: 13748461
    [No Abstract] [Full Text] [Related]

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