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114 related items for PubMed ID: 7099758

  • 1. Enzymologic studies and therapy of Leigh's disease associated with pyruvate decarboxylase deficiency.
    Toshima K, Kuroda Y, Hashimoto T, Ito M, Watanabe T, Miyao M, Ii K.
    Pediatr Res; 1982 Jun; 16(6):430-5. PubMed ID: 7099758
    [Abstract] [Full Text] [Related]

  • 2. Pyruvate decarboxylase deficiency in a patient with Leigh's encephalomyelopathy.
    Ohtake M, Takada G, Miyabayashi S, Arai N, Tada K, Morinaga S.
    Tohoku J Exp Med; 1982 Aug; 137(4):379-86. PubMed ID: 7123539
    [Abstract] [Full Text] [Related]

  • 3. 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 Aug; 2(1):15-8. PubMed ID: 6796755
    [Abstract] [Full Text] [Related]

  • 4. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.
    Miyabayashi S, Ito T, Narisawa K, Iinuma K, Tada K.
    Eur J Pediatr; 1985 Mar; 143(4):278-83. PubMed ID: 2985393
    [Abstract] [Full Text] [Related]

  • 5. [Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex].
    Siemes H, Goebel HH, Sengers RC, Ruitenbeek W, Trijbels JM.
    Monatsschr Kinderheilkd; 1987 Dec; 135(12):821-6. PubMed ID: 3125426
    [Abstract] [Full Text] [Related]

  • 6. Lactic acidosis in childhood.
    Israels S, Haworth JC, Dunn HG, Applegarth DA.
    Adv Pediatr; 1976 Dec; 22():267-303. PubMed ID: 178159
    [Abstract] [Full Text] [Related]

  • 7. Studies on pyruvate carboxylase, pyruvate decarboxylase and lipoamide dehydrogenase in subacute necrotizing encephalomyelopathy.
    Hansen TL, Christensen E, Brandt NJ.
    Acta Paediatr Scand; 1982 Mar; 71(2):263-7. PubMed ID: 6897146
    [Abstract] [Full Text] [Related]

  • 8. Partial pyruvate decarboxylase deficiency with profound lactic acidosis and hyperammonemia: responses to dichloroacetate and benzoate.
    McCormick K, Viscardi RM, Robinson B, Heininger J.
    Am J Med Genet; 1985 Oct; 22(2):291-9. PubMed ID: 4050860
    [Abstract] [Full Text] [Related]

  • 9. Episodic weakness in pyruvate decarboxylase deficiency.
    Evans OB.
    J Pediatr; 1984 Dec; 105(6):961-3. PubMed ID: 6502351
    [No Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.
    Tsuchiyama A, Oyanagi K, Hirano S, Tachi N, Sogawa H, Wagatsuma K, Nakao T, Tsugawa S, Kawamura Y.
    J Inherit Metab Dis; 1983 Apr; 6(3):85-8. PubMed ID: 6422150
    [Abstract] [Full Text] [Related]

  • 12. Normal activities of hepatic pyruvate dehydrogenase and pyruvate carboxylase in Leigh's syndrome.
    Tsuchiyama A, Oyanagi K, Sogawa H, Nakao T, Ogawa K, Fujita S.
    Tohoku J Exp Med; 1983 Jan; 139(1):67-72. PubMed ID: 6836560
    [Abstract] [Full Text] [Related]

  • 13. The effect of a high fat diet on pyruvate decarboxylase deficiency without central nervous system involvement.
    Kodama S, Yagi R, Ninomiya M, Goji K, Takahashi T, Morishita Y, Matsuo T.
    Brain Dev; 1983 Jan; 5(4):381-9. PubMed ID: 6416099
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Congenital lactic acidosis associated with pyruvate carboxylase deficiency.
    Sagy M, Barzilay Z, Barash V, Oren M, Vardi P, Cohen BE, Gutman A.
    Isr J Med Sci; 1981 Dec; 17(12):1159-63. PubMed ID: 6799424
    [Abstract] [Full Text] [Related]

  • 16. Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease.
    Atkin BM, Buist NR, Utter MF, Leiter AB, Banker BQ.
    Pediatr Res; 1979 Feb; 13(2):109-16. PubMed ID: 219411
    [Abstract] [Full Text] [Related]

  • 17. Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formula.
    Fattal-Valevski A, Kesler A, Sela BA, Nitzan-Kaluski D, Rotstein M, Mesterman R, Toledano-Alhadef H, Stolovitch C, Hoffmann C, Globus O, Eshel G.
    Pediatrics; 2005 Feb; 115(2):e233-8. PubMed ID: 15687431
    [Abstract] [Full Text] [Related]

  • 18. A deficiency of both subunits of pyruvate dehydrogenase which is not expressed in fibroblasts.
    Kerr DS, Berry SA, Lusk MM, Ho L, Patel MS.
    Pediatr Res; 1988 Jul; 24(1):95-100. PubMed ID: 3137520
    [Abstract] [Full Text] [Related]

  • 19. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.
    Oizumi J, Donnell GN, Ng WG, Mulivor RA, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1984 Jul; 38(1):80. PubMed ID: 6705569
    [No Abstract] [Full Text] [Related]

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