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205 related items for PubMed ID: 20065125

  • 21. Detection of 14-3-3 protein in the cerebrospinal fluid in mitochondrial encephalopathy with lactic acidosis and stroke-like episodes.
    Fujii K, Tanabe Y, Kobayashi K, Uchikawa H, Kohno Y.
    J Neurol Sci; 2005 Dec 15; 239(1):115-8. PubMed ID: 16213527
    [Abstract] [Full Text] [Related]

  • 22. Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes).
    Berbel-Garcia A, Barbera-Farre JR, Etessam JP, Salio AM, Cabello A, Gutierrez-Rivas E, Campos Y.
    Clin Neuropharmacol; 2004 Dec 15; 27(4):187-91. PubMed ID: 15319706
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
    Mimaki M, Hatakeyama H, Ichiyama T, Isumi H, Furukawa S, Akasaka M, Kamei A, Komaki H, Nishino I, Nonaka I, Goto Y.
    Mitochondrion; 2009 Apr 15; 9(2):115-22. PubMed ID: 19460299
    [Abstract] [Full Text] [Related]

  • 25. Cerebral blood flow in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.
    Ooiwa Y, Uematsu Y, Terada T, Nakai K, Itakura T, Komai N, Moriwaki H.
    Stroke; 1993 Feb 15; 24(2):304-9. PubMed ID: 8421833
    [Abstract] [Full Text] [Related]

  • 26. Focal hyperperfusion in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Case report.
    Amagasaki K, Shimizu T, Suzuki Y, Kakizawa T.
    J Neurosurg; 2001 Jan 15; 94(1):133-6. PubMed ID: 11147883
    [Abstract] [Full Text] [Related]

  • 27. Energy metabolism in disorders of the nervous system.
    Blass JP, Sheu RK, Cedarbaum JM.
    Rev Neurol (Paris); 1988 Jan 15; 144(10):543-63. PubMed ID: 2973643
    [Abstract] [Full Text] [Related]

  • 28. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
    Degoul F, Diry M, Pou-Serradell A, Lloreta J, Marsac C.
    Ann Neurol; 1994 Mar 15; 35(3):365-70. PubMed ID: 8122891
    [Abstract] [Full Text] [Related]

  • 29. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Di Trapani G, Gregori B, Servidei S, Ricci E, Sabatelli M, Tonali P.
    Clin Neuropathol; 1997 Mar 15; 16(4):195-200. PubMed ID: 9266144
    [Abstract] [Full Text] [Related]

  • 30. Single-gene stroke disorders.
    Majersik JJ, Skalabrin EJ.
    Semin Neurol; 2006 Feb 15; 26(1):33-48. PubMed ID: 16479442
    [Abstract] [Full Text] [Related]

  • 31. Headache and mitochondrial disorders.
    Rosen N.
    Headache; 2008 May 15; 48(5):733-4. PubMed ID: 18471127
    [Abstract] [Full Text] [Related]

  • 32. Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects.
    Tzoulis C, Bindoff LA.
    Brain; 2012 Dec 15; 135(Pt 12):3627-34. PubMed ID: 23065482
    [Abstract] [Full Text] [Related]

  • 33. 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
    [Abstract] [Full Text] [Related]

  • 34. [A case of MELAS associated with prosopagnosia, topographical disorientation and PLED].
    Funakawa I, Mukai K, Terao A, Kawashima S, Mori T.
    Rinsho Shinkeigaku; 1994 Oct 15; 34(10):1052-4. PubMed ID: 7834952
    [Abstract] [Full Text] [Related]

  • 35. Ocular motor disorders in mitochondrial encephalopathy with lactic acid and stroke-like episodes with the 3271 (T-C) point mutation in mitochondrial DNA.
    Shinmei Y, Kase M, Suzuki Y, Nitta T, Chin S, Yoshida K, Goto Y, Nagashima T, Ohno S.
    J Neuroophthalmol; 2007 Mar 15; 27(1):22-8. PubMed ID: 17414868
    [Abstract] [Full Text] [Related]

  • 36. Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases.
    Umaki Y, Mitsui T, Endo I, Akaike M, Matsumoto T.
    Acta Neuropathol; 2002 Feb 15; 103(2):163-70. PubMed ID: 11810183
    [Abstract] [Full Text] [Related]

  • 37. Hypothalamic growth hormone deficiency and supplementary GH therapy in two patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Matsuzaki M, Izumi T, Shishikura K, Suzuki H, Hirayama Y.
    Neuropediatrics; 2002 Oct 15; 33(5):271-3. PubMed ID: 12536371
    [Abstract] [Full Text] [Related]

  • 38. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ, Cruz-Martínez A, Campos-González Y, Gutiérrez-Molina M, Santiago-Pérez S, Pérez-Conde MC, López-Pajares MR, Martín-Casarrubias MA, Rubio-Muñoz JC, del Hoyo P, Arpa-Fernández A, Arenas-Barbero J.
    Rev Neurol; 2002 Oct 15; 41(8):449-54. PubMed ID: 16224730
    [Abstract] [Full Text] [Related]

  • 39. 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
    [Abstract] [Full Text] [Related]

  • 40. Deep white matter pathologic features in watershed regions: a novel pattern of central nervous system involvement in MELAS.
    Apostolova LG, White M, Moore SA, Davis PH.
    Arch Neurol; 2005 Jul 15; 62(7):1154-6. PubMed ID: 16009776
    [Abstract] [Full Text] [Related]

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