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Journal Abstract Search

199 related items for PubMed ID: 26711613

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  • 7. Adult-onset of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presenting as acute meningoencephalitis: a case report.
    Hsu YC, Yang FC, Perng CL, Tso AC, Wong LJ, Hsu CH.
    J Emerg Med; 2012 Sep; 43(3):e163-6. PubMed ID: 20036095
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  • 8. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R, Zárate-Moysen A, Monsalvo-Reyes A, Herrero MD, Ruiz-Pesini E, López-Pérez M, Montoya J, Montiel-Sosa JF.
    Rev Neurol; 2012 Sep; 44(1):18-22. PubMed ID: 17199225
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  • 12. The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
    Nishino I, Komatsu M, Kodama S, Horai S, Nonaka I, Goto Y.
    Muscle Nerve; 1996 Dec; 19(12):1603-4. PubMed ID: 8941275
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  • 15. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
    Marotta R, Reardon K, McKelvie PA, Chiotis M, Chin J, Cook M, Collins SJ.
    J Clin Neurosci; 2009 Sep; 16(9):1223-5. PubMed ID: 19502062
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  • 16. 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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  • 17. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
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