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Journal Abstract Search

164 related items for PubMed ID: 6402999

  • 1. Leigh's necrotizing encephalopathy with pyruvate carboxylase deficiency.
    Gilbert EF, Arya S, Chun R.
    Arch Pathol Lab Med; 1983 Apr; 107(4):162-6. PubMed ID: 6402999
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  • 2. Pyruvate carboxylase activity in subacute necrotizing encephalopathy (Leigh's disease).
    Sander J, Packman S, Berg BO, Hutchison HT, Caswell N.
    Neurology; 1984 Apr; 34(4):515-6. PubMed ID: 6538306
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  • 3. Lactic acidosis in childhood.
    Israels S, Haworth JC, Dunn HG, Applegarth DA.
    Adv Pediatr; 1976 Apr; 22():267-303. PubMed ID: 178159
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  • 9. Pyruvate carboxylase deficiency: an alleged biochemical cause of Leigh's disease.
    Murphy JV, Isohashi F, Weinberg MB, Utter MF.
    Pediatrics; 1981 Sep; 68(3):401-4. PubMed ID: 6792586
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  • 10. [Subacute necrotizing encephalopathy, Leigh's disease. Apropos of a case].
    Delisle MB, Netter JC, Peyrille F, Bouissou H.
    Ann Pathol; 1985 Sep; 5(4-5):313-7. PubMed ID: 3833250
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  • 11. Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.
    Prick MJ, Gabreëls FJ, Renier WO, Trijbels JM, Willems JL, Janssen AJ, Slooff JL, Geelen JA, de Jager JP.
    Neuropediatrics; 1982 May; 13(2):108-11. PubMed ID: 6813759
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  • 12. Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase.
    Van Biervliet JP, Duran M, Wadman SK, Koster JF, van Rossum A.
    J Inherit Metab Dis; 1980 May; 2(1):15-8. PubMed ID: 6796755
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  • 19. Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy.
    Mochel F, DeLonlay P, Touati G, Brunengraber H, Kinman RP, Rabier D, Roe CR, Saudubray JM.
    Mol Genet Metab; 2005 Apr; 84(4):305-12. PubMed ID: 15781190
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  • 20. Neurochemical changes in Leigh's disease.
    Murphy JV.
    J Nutr Sci Vitaminol (Tokyo); 1976 Aug; 22 SUPPL():69-73. PubMed ID: 185345
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