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Journal Abstract Search

178 related items for PubMed ID: 6897695

  • 41. Characterization of molecular defects in isovaleryl-CoA dehydrogenase in patients with isovaleric acidemia.
    Mohsen AW, Anderson BD, Volchenboum SL, Battaile KP, Tiffany K, Roberts D, Kim JJ, Vockley J.
    Biochemistry; 1998 Jul 14; 37(28):10325-35. PubMed ID: 9665741
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  • 42. Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia.
    Lee YW, Lee DH, Vockley J, Kim ND, Lee YK, Ki CS.
    Mol Genet Metab; 2007 Jul 14; 92(1-2):71-7. PubMed ID: 17576084
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  • 48. Stable isotope dilution analysis of isovalerylglycine in amniotic fluid and urine and its application for the prenatal diagnosis of isovaleric acidemia.
    Hine DG, Hack AM, Goodman SI, Tanaka K.
    Pediatr Res; 1986 Mar 14; 20(3):222-6. PubMed ID: 3703611
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  • 53. Isovaleric acidemia. Clinical presentation of 6 cases.
    Tokatli A, Coşkun T, Ozalp I.
    Turk J Pediatr; 1998 Mar 14; 40(1):111-9. PubMed ID: 9673537
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  • 58. 3-Hydroxyisoheptanoic acid: a new metabolite in isovaleric acidemia.
    Lehnert W.
    Clin Chim Acta; 1981 Jun 02; 113(1):101-3. PubMed ID: 7237839
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  • 59. Cerebral energy metabolism in isovaleric acidaemia.
    Lorek AK, Penrice JM, Cady EB, Leonard JV, Wyatt JS, Iles RA, Burns SP, Reynolds EO.
    Arch Dis Child Fetal Neonatal Ed; 1996 May 02; 74(3):F211-3. PubMed ID: 8777688
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  • 60. Isovaleric acidemia. Clinical features of a new genetic defect of leucine metabolism.
    Budd MA, Tanaka K, Holmes LB, Efron ML, Crawford JD, Isselbacher KJ.
    N Engl J Med; 1967 Aug 17; 277(7):321-7. PubMed ID: 4378266
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