BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 1849240)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants.
    Tiranti V; Munaro M; Sandonà D; Lamantea E; Rimoldi M; DiDonato S; Bisson R; Zeviani M
    Hum Mol Genet; 1995 Nov; 4(11):2017-23. PubMed ID: 8589677
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndrome.
    Munaro M; Tiranti V; Sandonà D; Lamantea E; Uziel G; Bisson R; Zeviani M
    Hum Mol Genet; 1997 Feb; 6(2):221-8. PubMed ID: 9063742
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.
    Adams PL; Lightowlers RN; Turnbull DM
    Ann Neurol; 1997 Feb; 41(2):268-70. PubMed ID: 9029077
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Cytochrome c oxidase deficiency.
    DiMauro S; Lombes A; Nakase H; Mita S; Fabrizi GM; Tritschler HJ; Bonilla E; Miranda AF; DeVivo DC; Schon EA
    Pediatr Res; 1990 Nov; 28(5):536-41. PubMed ID: 2175026
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency.
    Moslemi AR; Tulinius M; Darin N; Aman P; Holme E; Oldfors A
    Neurology; 2003 Oct; 61(7):991-3. PubMed ID: 14557577
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency.
    Yao J; Shoubridge EA
    Hum Mol Genet; 1999 Dec; 8(13):2541-9. PubMed ID: 10556303
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Leigh's syndrome and mitochondrial myopathy].
    Nakase H
    Nihon Rinsho; 1993 Sep; 51(9):2403-8. PubMed ID: 8411720
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome.
    Vazquez-Memije ME; Shanske S; Santorelli FM; Kranz-Eble P; Davidson E; DeVivo DC; DiMauro S
    J Inherit Metab Dis; 1996; 19(1):43-50. PubMed ID: 8830176
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.