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156 related items for PubMed ID: 3612192

  • 1. Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
    van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Lamers KJ, Sloof JL.
    J Neurol; 1987 May; 234(4):215-9. PubMed ID: 3612192
    [Abstract] [Full Text] [Related]

  • 2. [Leigh's syndrome].
    Sunohara N.
    Nihon Rinsho; 1990 Jul; 48(7):1568-72. PubMed ID: 2169544
    [No Abstract] [Full Text] [Related]

  • 3. Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver.
    Van Erven PM, Gabreëls FJ, Ruitenbeek W, Den Hartog MR, Fischer JC, Renier WO, Trijbels JM, Slooff JL, Janssen AJ.
    Acta Neurol Scand; 1985 Jul; 72(1):36-42. PubMed ID: 4050316
    [Abstract] [Full Text] [Related]

  • 4. Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).
    van Erven PM, Ruitenbeek W, Gabreëls FJ, Renier WO, Fischer JC, Janssen AJ.
    Neuropediatrics; 1986 Feb; 17(1):28-32. PubMed ID: 3008021
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy.
    Arts WF, Scholte HR, Loonen MC, Przyrembel H, Fernandes J, Trijbels JM, Luyt-Houwen IE.
    J Neurol Sci; 1987 Jan; 77(1):103-15. PubMed ID: 3027266
    [Abstract] [Full Text] [Related]

  • 7. [Subacute necrotizing encephalopathy, Leigh's disease. Apropos of a case].
    Delisle MB, Netter JC, Peyrille F, Bouissou H.
    Ann Pathol; 1985 Jan; 5(4-5):313-7. PubMed ID: 3833250
    [Abstract] [Full Text] [Related]

  • 8. [Current developments in the clinical diagnosis and the biochemical analysis of Leigh's syndrome].
    Arts WF.
    Tijdschr Kindergeneeskd; 1989 Jun; 57(3):97-101. PubMed ID: 2799800
    [Abstract] [Full Text] [Related]

  • 9. Intravenous pyruvate loading test in Leigh syndrome.
    Van Erven PM, Gabreëls FJ, Wevers RA, Doesburg WH, Ruitenbeek W, Renier WO, Lamers KJ.
    J Neurol Sci; 1987 Feb; 77(2-3):217-27. PubMed ID: 3819766
    [Abstract] [Full Text] [Related]

  • 10. Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia.
    Martin JJ, Van de Vyver FL, Scholte HR, Roodhooft AM, Ceuterick C, Martin L, Luyt-Houwen IE.
    J Neurol Sci; 1988 Apr; 84(2-3):189-200. PubMed ID: 3379446
    [Abstract] [Full Text] [Related]

  • 11. [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]

  • 12. Systems analysis of energy metabolism elucidates the affected respiratory chain complex in Leigh's syndrome.
    Vo TD, Paul Lee WN, Palsson BO.
    Mol Genet Metab; 2007 May; 91(1):15-22. PubMed ID: 17336115
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial abnormalities in choroid plexus of Leigh disease.
    Ohama E, Ikuta F, Nakamura N.
    Brain Dev; 1988 May; 10(1):30-5. PubMed ID: 3285724
    [Abstract] [Full Text] [Related]

  • 14. Deficiency of pyruvate dehydrogenase complex (PDHC) in Leigh's disease fibroblasts: an abnormality in lipoamide dehydrogenase affecting PDHC activation.
    Hinman LM, Sheu KF, Baker AC, Kim YT, Blass JP.
    Neurology; 1989 Jan; 39(1):70-5. PubMed ID: 2909916
    [Abstract] [Full Text] [Related]

  • 15. Proton spectroscopy in five patients with Leigh's disease and mitochondrial enzyme deficiency.
    Krägeloh-Mann I, Grodd W, Schöning M, Marquard K, Nägele T, Ruitenbeek W.
    Dev Med Child Neurol; 1993 Sep; 35(9):769-76. PubMed ID: 7689066
    [Abstract] [Full Text] [Related]

  • 16. Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease.
    Glerum M, Robinson BH, Spratt C, Wilson J, Patrick D.
    Am J Hum Genet; 1987 Oct; 41(4):584-93. PubMed ID: 2821802
    [Abstract] [Full Text] [Related]

  • 17. Leigh's disease--several nosological entities with an identical histopathological complex?
    Walter GF, Brucher JM, Martin JJ, Ceuterick C, Pilz P, Freund M.
    Neuropathol Appl Neurobiol; 1986 Oct; 12(1):95-107. PubMed ID: 3703157
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. [Suspected pyruvate carboxylase deficiency in 4 children with Leigh disease].
    Pronicka E, Kulczycka H, Chmielik J, Krajewska G, Szeffer J.
    Neurol Neurochir Pol; 1986 Jan; 20(2):89-94. PubMed ID: 3095672
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.
    van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Fischer JC.
    Arch Neurol; 1987 Jul; 44(7):775-8. PubMed ID: 3593065
    [Abstract] [Full Text] [Related]

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