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Journal Abstract Search

323 related items for PubMed ID: 28883258

  • 1. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
    Mukai M, Nagata E.
    Intern Med; 2017 Oct 01; 56(19):2695. PubMed ID: 28883258
    [No Abstract] [Full Text] [Related]

  • 2. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
    Finsterer J, Zarrouk-Mahjoub S.
    Intern Med; 2017 Oct 01; 56(19):2693. PubMed ID: 28883250
    [No Abstract] [Full Text] [Related]

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  • 4. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes due to m.3243A > G mutation in a 76-year-old woman.
    Ueki K, Wakisaka Y, Nakamura K, Shono Y, Wada S, Yoshikawa Y, Matsukuma Y, Uchiumi T, Kang D, Kitazono T, Ago T.
    J Neurol Sci; 2020 May 15; 412():116791. PubMed ID: 32224343
    [No Abstract] [Full Text] [Related]

  • 5. Mitochondrial Encephalopathy and Optic Neuropathy Due to m.10158 MT-ND3 Complex I Mutation Presenting in an Adult Patient: Case Report and Review of the Literature.
    Vodopivec I, Cho TA, Rizzo JF, Frosch MP, Sims KB.
    Neurologist; 2016 Jul 15; 21(4):61-5. PubMed ID: 27348141
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  • 9. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun 15; 51(6):1425-8. PubMed ID: 8320824
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  • 10. An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu(UUR)) gene presenting cardiac dysfunction as the main symptom.
    Higashikata T, Koyama J, Shimada H, Yazaki M, Owa M, Ikeda S.
    Intern Med; 2001 May 15; 40(5):405-8. PubMed ID: 11393411
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  • 12. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 15; 51(9):2373-8. PubMed ID: 8411715
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint).
    Wang S, Song T, Wang S.
    Medicine (Baltimore); 2020 Jun 12; 99(24):e20310. PubMed ID: 32541454
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  • 15. 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 12; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 16. Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap.
    Liu F, Zhang D, Yan C.
    Neurol India; 2016 Mar 12; 64(2):336-8. PubMed ID: 26954819
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  • 17. When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?
    Lorenzoni PJ, Werneck LC, Kay CS, Silvado CE, Scola RH.
    Arq Neuropsiquiatr; 2015 Nov 12; 73(11):959-67. PubMed ID: 26517220
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  • 18. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
    Li JY, Hsieh RH, Peng NJ, Lai PH, Lee CF, Lo YK, Wei YH.
    J Formos Med Assoc; 2007 Jul 12; 106(7):528-36. PubMed ID: 17660142
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  • 19. [MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes)].
    Goto Y.
    Ryoikibetsu Shokogun Shirizu; 2001 Jul 12; (36):146-9. PubMed ID: 11596349
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  • 20. Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C.
    Kori A, Hori I, Tanaka T, Aoyama K, Ito K, Hattori A, Ban K, Okazaki Y, Murayama K, Saitoh S.
    Brain Dev; 2019 Oct 12; 41(9):803-807. PubMed ID: 31178082
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