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Journal Abstract Search

100 related items for PubMed ID: 11596345

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

  • 2. [Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].
    Monnot S, Chabrol B, Cano A, Pellissier JF, Collignon P, Montfort MF, Paquis-Flucklinger V.
    Arch Pediatr; 2005 May; 12(5):568-71. PubMed ID: 15885549
    [Abstract] [Full Text] [Related]

  • 3. [Electron transfer complex IV (cytochrome c oxidase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 1998 May; (19 Pt 2):497-500. PubMed ID: 9645119
    [No Abstract] [Full Text] [Related]

  • 4. Cytochrome c oxidase deficiency.
    Shoubridge EA.
    Am J Med Genet; 2001 May; 106(1):46-52. PubMed ID: 11579424
    [Abstract] [Full Text] [Related]

  • 5. [Cytochrome c oxidase deficiency--SURF1 mutations].
    Naito E, Ogawa Y.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():446-9. PubMed ID: 12013909
    [No Abstract] [Full Text] [Related]

  • 6. [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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  • 9. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
    Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR.
    Chin Med J (Engl); 2006 Mar 05; 119(5):373-7. PubMed ID: 16542579
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  • 11. High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients.
    Piekutowska-Abramczuk D, Popowska E, Pronicki M, Karczmarewicz E, Tylek-Lemanska D, Sykut-Cegielska J, Szymanska-Dembinska T, Bielecka L, Krajewska-Walasek M, Pronicka E.
    Eur J Paediatr Neurol; 2009 Mar 05; 13(2):146-53. PubMed ID: 18583168
    [Abstract] [Full Text] [Related]

  • 12. LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.
    Debray FG, Morin C, Janvier A, Villeneuve J, Maranda B, Laframboise R, Lacroix J, Decarie JC, Robitaille Y, Lambert M, Robinson BH, Mitchell GA.
    J Med Genet; 2011 Mar 05; 48(3):183-9. PubMed ID: 21266382
    [Abstract] [Full Text] [Related]

  • 13. [Leigh's syndrome and mitochondrial myopathy].
    Nakase H.
    Nihon Rinsho; 1993 Sep 05; 51(9):2403-8. PubMed ID: 8411720
    [Abstract] [Full Text] [Related]

  • 14. Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency.
    Tay SK, Nesti C, Mancuso M, Schon EA, Shanske S, Bonilla E, Davidson MM, Dimauro S.
    Arch Neurol; 2004 Dec 05; 61(12):1935-7. PubMed ID: 15596615
    [Abstract] [Full Text] [Related]

  • 15. [Cytochrome c oxidase deficiency].
    Miyabayashi S.
    Tanpakushitsu Kakusan Koso; 1988 Apr 05; 33(5):831-3. PubMed ID: 2855956
    [No Abstract] [Full Text] [Related]

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  • 17. 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 05; 22(7):858-62. PubMed ID: 17715279
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  • 19. [Complex III (ubiquinone-cytochrome c reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul 05; (36):135-6. PubMed ID: 11596344
    [No Abstract] [Full Text] [Related]

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