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Journal Abstract Search

107 related items for PubMed ID: 11596344

  • 1. [Complex III (ubiquinone-cytochrome c reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):135-6. PubMed ID: 11596344
    [No Abstract] [Full Text] [Related]

  • 2. [Complex III deficiency due to mutations in the cytochrome b gene].
    Ishii A, Ohkoshi N.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():337-40. PubMed ID: 12013880
    [No Abstract] [Full Text] [Related]

  • 3. Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient.
    Blázquez A, Gil-Borlado MC, Morán M, Verdú A, Cazorla-Calleja MR, Martín MA, Arenas J, Ugalde C.
    Neuromuscul Disord; 2009 Feb; 19(2):143-6. PubMed ID: 19162478
    [Abstract] [Full Text] [Related]

  • 4. The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.
    Haut S, de Villemeur TB, Brivet M, Guiochon-Mantel A, Boutron A, Rustin P, Legrand A, Slama A.
    Eur J Hum Genet; 2004 Mar; 12(3):220-4. PubMed ID: 14735157
    [Abstract] [Full Text] [Related]

  • 5. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Mar; (36):129-31. PubMed ID: 11596342
    [No Abstract] [Full Text] [Related]

  • 6. Inhibition of mitochondrial complex IV leads to secondary loss complex II-III activity: implications for the pathogenesis and treatment of mitochondrial encephalomyopathies.
    Hargreaves IP, Duncan AJ, Wu L, Agrawal A, Land JM, Heales SJ.
    Mitochondrion; 2007 Jul; 7(4):284-7. PubMed ID: 17395552
    [Abstract] [Full Text] [Related]

  • 7. [Complex IV (cytochrome c oxidase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul; (36):137-41. PubMed ID: 11596345
    [No Abstract] [Full Text] [Related]

  • 8. [Electron transfer complex III deficiency].
    Nishino I, Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul; (19 Pt 2):494-6. PubMed ID: 9645118
    [No Abstract] [Full Text] [Related]

  • 9. [Electron transfer complex I deficiency].
    Goto Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Jul; (19 Pt 2):488-90. PubMed ID: 9645116
    [No Abstract] [Full Text] [Related]

  • 10. [Coenzyme Q10 deficiency].
    Imataka G, Yamanouchi H.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():462-5. PubMed ID: 12013914
    [No Abstract] [Full Text] [Related]

  • 11. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
    Thyagarajan D, Byrne E.
    Int Rev Neurobiol; 2002 Apr; 53():93-144. PubMed ID: 12512338
    [No Abstract] [Full Text] [Related]

  • 12. [West syndrome associated with deficit of complex III of the respiratory mitochondrial chain].
    Castro-Gago M, Pavón Belinchón P, Fernández Seara J, Rodrigo Sáez E, Beiras Iglesias A, Pérez Sánchez A.
    An Esp Pediatr; 1993 Apr; 38(4):355-8. PubMed ID: 8386913
    [No Abstract] [Full Text] [Related]

  • 13. Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report.
    Montero R, Sánchez-Alcázar JA, Briones P, Navarro-Sastre A, Gallardo E, Bornstein B, Herrero-Martín D, Rivera H, Martin MA, Marti R, García-Cazorla A, Montoya J, Navas P, Artuch R.
    Clin Biochem; 2009 May; 42(7-8):742-5. PubMed ID: 19094978
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
    Pancrudo J, Shanske S, Bonilla E, Daras M, Akman HO, Krishna S, Malkin E, DiMauro S.
    J Child Neurol; 2007 Jul; 22(7):858-62. PubMed ID: 17715279
    [Abstract] [Full Text] [Related]

  • 15. Mutations in respiratory chain complexes and human diseases.
    Borisov VB.
    Ital J Biochem; 2004 Mar; 53(1):34-40. PubMed ID: 15356960
    [Abstract] [Full Text] [Related]

  • 16. Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene.
    Ramos-Arroyo MA, Hualde J, Ayechu A, De Meirleir L, Seneca S, Nadal N, Briones P.
    Clin Genet; 2009 Jun; 75(6):585-7. PubMed ID: 19508421
    [No Abstract] [Full Text] [Related]

  • 17. [Complex II (succinate-ubiquinone reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Jun; (36):132-4. PubMed ID: 11596343
    [No Abstract] [Full Text] [Related]

  • 18. [Complex III].
    Koga Y, Fukiyama R.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():486-9. PubMed ID: 12013920
    [No Abstract] [Full Text] [Related]

  • 19. Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency.
    Meulemans A, Lissens W, Van Coster R, De Meirleir L, Smet J, Nassogne MC, Liebaers I, Seneca S.
    Eur J Paediatr Neurol; 2004 Apr; 8(6):299-306. PubMed ID: 15542384
    [Abstract] [Full Text] [Related]

  • 20. [Complex IV(cytochrome c oxidase)].
    Sugie K, Nishino I.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():490-4. PubMed ID: 12013921
    [No Abstract] [Full Text] [Related]

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