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Journal Abstract Search

168 related items for PubMed ID: 10953189

  • 21. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.
    Scaglia F, Northrop JL.
    CNS Drugs; 2006; 20(6):443-64. PubMed ID: 16734497
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  • 22. Myocardial flow regulation in people with mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes/myoclonic epilepsy and ragged red fibers and other mitochondrial syndromes.
    Tawakol A, Sims K, MacRae C, Friedman JR, Alpert NM, Fischman AJ, Gewirtz H.
    Coron Artery Dis; 2003 May; 14(3):197-205. PubMed ID: 12702922
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  • 23. MELAS and L-arginine therapy: pathophysiology of stroke-like episodes.
    Koga Y, Povalko N, Nishioka J, Katayama K, Kakimoto N, Matsuishi T.
    Ann N Y Acad Sci; 2010 Jul; 1201():104-10. PubMed ID: 20649546
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  • 28. Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy.
    Haginoya K, Miyabayashi S, Iinuma K, Tada K.
    Acta Neuropathol; 1993 Jul; 85(4):370-7. PubMed ID: 8386896
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  • 30. Different mitochondrial genetic defects exhibit the same protein signature of metabolism in skeletal muscle of PEO and MELAS patients: A role for oxidative stress.
    Santacatterina F, Torresano L, Núñez-Salgado A, Esparza-Molto PB, Olive M, Gallardo E, García-Arumi E, Blazquez A, González-Quintana A, Martín MA, Cuezva JM.
    Free Radic Biol Med; 2018 Oct; 126():235-248. PubMed ID: 30138712
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  • 36. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
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