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Journal Abstract Search

170 related items for PubMed ID: 16006433

  • 1. A juvenile case of MELAS with T3271C mitochondrial DNA mutation.
    Stenqvist L, Paetau A, Valanne L, Suomalainen A, Pihko H.
    Pediatr Res; 2005 Aug; 58(2):258-62. PubMed ID: 16006433
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  • 2. 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
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  • 4. 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; 61(2):269-72. PubMed ID: 14967777
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  • 5. 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
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  • 8. 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; 34(3):235-8. PubMed ID: 16504796
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  • 11. 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 Mar; 94(1-2):42-7. PubMed ID: 7613232
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  • 13. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A.
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
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  • 14. New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS).
    Calvaruso MA, Willemsen MA, Rodenburg RJ, van den Brand M, Smeitink JA, Nijtmans L.
    Mitochondrion; 2011 Sep; 11(5):778-82. PubMed ID: 21704194
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  • 15. 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; 63(1):71-6. PubMed ID: 10645055
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  • 16. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
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  • 17. 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 15; 110(11):851-5. PubMed ID: 9772417
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  • 18. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov 15; 122(11):978-81. PubMed ID: 9822126
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  • 19. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; 1998 Nov 15; 33(2):148-50. PubMed ID: 11562875
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  • 20. A mitochondrial DNA mutation in a patient with an extensive family history of Duchenne muscular dystrophy.
    Wong LJ, Wladyka C, Mardach-Verdon R.
    Muscle Nerve; 2004 Jul 15; 30(1):118-22. PubMed ID: 15221888
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