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596 related items for PubMed ID: 7684581

  • 1. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 2. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Murakami T, Kumamoto T, Uchino M, Nonaka I, Ando M.
    Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial DNA and RNA processing in MELAS.
    Kaufmann P, Koga Y, Shanske S, Hirano M, DiMauro S, King MP, Schon EA.
    Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598
    [Abstract] [Full Text] [Related]

  • 4. [Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy].
    Li YF, Wang ZX, Gao XG, Hong DJ, Yuan Y.
    Zhonghua Yi Xue Za Zhi; 2009 Jun 16; 89(23):1593-6. PubMed ID: 19957502
    [Abstract] [Full Text] [Related]

  • 5. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
    [Abstract] [Full Text] [Related]

  • 6. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan 13; 63(1):71-6. PubMed ID: 10645055
    [Abstract] [Full Text] [Related]

  • 7. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar 13; 34(3):235-8. PubMed ID: 16504796
    [Abstract] [Full Text] [Related]

  • 8. Isolated cytochrome c oxidase deficiency as a cause of MELAS.
    Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE.
    J Med Genet; 2008 Feb 13; 45(2):117-21. PubMed ID: 18245391
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct 13; 5(5):622-32. PubMed ID: 1392136
    [Abstract] [Full Text] [Related]

  • 10. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A.
    Brain; 2006 May 13; 129(Pt 5):1249-59. PubMed ID: 16537564
    [Abstract] [Full Text] [Related]

  • 11. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Hess JF, Parisi MA, Bennett JL, Clayton DA.
    Nature; 1991 May 16; 351(6323):236-9. PubMed ID: 1755869
    [Abstract] [Full Text] [Related]

  • 12. [Vascular pathology in chronic progressive external ophthalmoplegia with ragged-red fibers].
    Hasegawa H, Matsuoka T, Goto Y, Nonaka I.
    Rinsho Shinkeigaku; 1992 Feb 16; 32(2):155-60. PubMed ID: 1611773
    [Abstract] [Full Text] [Related]

  • 13. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R.
    Arch Neurol; 2004 Feb 16; 61(2):269-72. PubMed ID: 14967777
    [Abstract] [Full Text] [Related]

  • 14. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec 16; 156(12):1136-47. PubMed ID: 11139730
    [Abstract] [Full Text] [Related]

  • 15. [Strongly succinate dehydrogenase-reactive blood vessels (SSV) in various neuromuscular diseases].
    Matsuoka T, Hasegawa H, Nonaka I.
    Rinsho Shinkeigaku; 1992 Jun 16; 32(6):645-7. PubMed ID: 1424348
    [Abstract] [Full Text] [Related]

  • 16. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 16; 51(9):2373-8. PubMed ID: 8411715
    [Abstract] [Full Text] [Related]

  • 17. Heteroplasmic mitochondrial DNA mutation in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Chiang LM, Jong YJ, Huang SC, Tsai JL, Pang CY, Lee HC, Wei YH.
    J Formos Med Assoc; 1995 Sep 16; 94(1-2):42-7. PubMed ID: 7613232
    [Abstract] [Full Text] [Related]

  • 18. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R, Reilmann R, Holinski-Feder E, Ringelstein EB, Klopstock T.
    Neuromuscul Disord; 2008 Jul 16; 18(7):553-6. PubMed ID: 18590963
    [Abstract] [Full Text] [Related]

  • 19. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W, Hayasaka K, Shoji Y, Takahashi T, Takada G, Saito M, Fukawa O, Wachi E.
    Biochem Mol Biol Int; 1994 Aug 16; 33(6):1055-61. PubMed ID: 7804130
    [Abstract] [Full Text] [Related]

  • 20. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov 16; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

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