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PUBMED FOR HANDHELDS

Journal Abstract Search


238 related items for PubMed ID: 5229850

  • 41.
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  • 44. The occurrence of beta-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia.
    Stokke O, Jellum E, Eldjarn L, Schnitler R.
    Clin Chim Acta; 1973 May 30; 45(4):391-401. PubMed ID: 4730209
    [No Abstract] [Full Text] [Related]

  • 45. Prenatal diagnosis and a case report of isovaleric acidaemia.
    Blaskovics ME, Ng WG, Donnell GN.
    J Inherit Metab Dis; 1978 May 30; 1(1):9-11. PubMed ID: 117238
    [No Abstract] [Full Text] [Related]

  • 46. [2-Methyl-3-oxovaleric acid: a characteristic metabolite in propionic acidemia].
    Lehnert W, Junker A.
    Clin Chim Acta; 1980 May 21; 104(1):47-51. PubMed ID: 7389125
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  • 47. Endogenous catabolism as source of toxic metabolites in isovaleric acidemia.
    Pollitt RJ.
    J Pediatr; 1987 Sep 21; 111(3):477-8. PubMed ID: 3625423
    [No Abstract] [Full Text] [Related]

  • 48. Biosynthesis of triacylglycerols containing isovaleric acid.
    Malins DC, Robisch PA, Varanasi U.
    Biochem Biophys Res Commun; 1972 Jul 25; 48(2):314-9. PubMed ID: 5043185
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  • 49. Isovaleric acidemia: report of one case.
    Hou JW, Wang TR.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1990 Jul 25; 31(4):262-5. PubMed ID: 2124776
    [Abstract] [Full Text] [Related]

  • 50. New metabolites in isovaleric acidemia.
    Truscott RJ, Malegan D, McCairns E, Burke D, Hick L, Sims P, Halpern B, Tanaka K, Sweetman L, Nyhan WL, Hammond J, Bumack C, Haan EA, Danks DM.
    Clin Chim Acta; 1981 Mar 05; 110(2-3):187-203. PubMed ID: 6452974
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  • 53. Possibility of inborn defect in isovalericacidaemia involving altered enzyme specificity rather than total inactivity.
    Engel PC.
    Nature; 1974 Mar 08; 248(5444):140-2. PubMed ID: 4818917
    [No Abstract] [Full Text] [Related]

  • 54. Neonatal lethargy due to isovaleric acidemia and hyperammonemia.
    Mendiola J, Robotham JL, Liehr JG, Williams JC.
    Tex Med; 1984 Jan 08; 80(1):52-4. PubMed ID: 6695347
    [No Abstract] [Full Text] [Related]

  • 55. Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.
    Duran M, Beemer FA, Tibosch AS, Bruinvis L, Ketting D, Wadman SK.
    J Pediatr; 1982 Oct 08; 101(4):551-4. PubMed ID: 6181239
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  • 56.
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  • 57.
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  • 58. Excretion of tiglylglycine in propionic acidemia.
    Rasmussen K, Ando T, Nyhan WL, Hull D, Cottom D, Kilroy AW, Wadlington W.
    J Pediatr; 1972 Nov 08; 81(5):970-2. PubMed ID: 5086724
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  • 59.
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  • 60. Hyperammonaemia in a preterm infant with isovaleric acidaemia.
    Wilson WG, Audenaert SM, Squillaro EJ.
    J Inherit Metab Dis; 1984 Nov 08; 7(2):71. PubMed ID: 6434830
    [No Abstract] [Full Text] [Related]


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