BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 2828763)

  • 1. Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.
    Miyabayashi S; Ito T; Abukawa D; Narisawa K; Tada K; Tanaka M; Ozawa T; Droste M; Kadenbach B
    J Inherit Metab Dis; 1987; 10(3):289-92. PubMed ID: 2828763
    [No Abstract]   [Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytochrome c oxidase deficiency in three patients with Leigh's disease.
    Di Rocco M; Veneselli E; Ciccone MO; Taccone A; Stroppiano M; Cottafava F
    J Inherit Metab Dis; 1988; 11 Suppl 2():189-92. PubMed ID: 2846961
    [No Abstract]   [Full Text] [Related]  

  • 5. Cytochrome c oxidase deficiency in Leigh syndrome.
    DiMauro S; Servidei S; Zeviani M; DiRocco M; DeVivo DC; DiDonato S; Uziel G; Berry K; Hoganson G; Johnsen SD
    Ann Neurol; 1987 Oct; 22(4):498-506. PubMed ID: 2829705
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cytochrome C oxidase deficiency in two siblings with Leigh encephalomyelopathy.
    Miyabayashi S; Narisawa K; Iinuma K; Tada K; Sakai K; Kobayashi K; Kobayashi Y; Morinaga S
    Brain Dev; 1984; 6(4):362-72. PubMed ID: 6093613
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).
    Hayasaka K; Brown GK; Danks DM; Droste M; Kadenbach B
    J Inherit Metab Dis; 1989; 12(3):247-56. PubMed ID: 2559245
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy.
    Koga Y; Nonaka I; Nakao M; Yoshino M; Tanaka M; Ozawa T; Nakase H; DiMauro S
    J Neurol Sci; 1990 Jan; 95(1):63-76. PubMed ID: 2159985
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.
    Reichmann H; Scheel H; Bier B; Ketelsen UP; Zabransky S
    Ann Neurol; 1992 Jan; 31(1):107-9. PubMed ID: 1311909
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy.
    Haginoya K; Miyabayashi S; Iinuma K; Okino E; Maesaka H; Tada K
    Pediatr Neurol; 1992; 8(1):13-8. PubMed ID: 1313674
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.
    Lombes A; Nakase H; Tritschler HJ; Kadenbach B; Bonilla E; DeVivo DC; Schon EA; DiMauro S
    Neurology; 1991 Apr; 41(4):491-8. PubMed ID: 1849240
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.
    Miranda AF; Ishii S; DiMauro S; Shay JW
    Neurology; 1989 May; 39(5):697-702. PubMed ID: 2540452
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).
    Kustermann-Kuhn B; Harzer K; Schröder R; Permanetter W; Peiffer J
    Hum Genet; 1984; 68(1):51-3. PubMed ID: 6437963
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Defect of NADH dehydrogenase in Leigh syndrome.
    Van Erven PM; Fischer JC; Gabreëls FJ; Renier WO; Trijbels JM; Janssen AJ
    Acta Neurol Scand; 1986 Aug; 74(2):167. PubMed ID: 3776463
    [No Abstract]   [Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease.
    Robinson BH; De Meirleir L; Glerum M; Sherwood G; Becker L
    J Pediatr; 1987 Feb; 110(2):216-22. PubMed ID: 3027293
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 7.