These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 6093613)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec.
    Merante F; Petrova-Benedict R; MacKay N; Mitchell G; Lambert M; Morin C; De Braekeleer M; Laframboise R; Gagné R; Robinson BH
    Am J Hum Genet; 1993 Aug; 53(2):481-7. PubMed ID: 8392290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenetic speculations.
    Van Coster R; Lombres A; De Vivo DC; Chi TL; Dodson WE; Rothman S; Orrechio EJ; Grover W; Berry GT; Schwartz JF
    J Neurol Sci; 1991 Jul; 104(1):97-111. PubMed ID: 1655984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome.
    Brown RM; Brown GK
    J Inherit Metab Dis; 1996; 19(6):752-60. PubMed ID: 8982948
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect.
    Medina L; Chi TL; DeVivo DC; Hilal SK
    AJR Am J Roentgenol; 1990 Jun; 154(6):1269-74. PubMed ID: 2159689
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leigh encephalopathy: histologic and biochemical analyses of muscle biopsies.
    Nagai T; Goto Y; Matsuoka T; Sakuta R; Naito E; Kuroda Y; Nonaka I
    Pediatr Neurol; 1992; 8(5):328-32. PubMed ID: 1329789
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.