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Journal Abstract Search

143 related items for PubMed ID: 28883250

  • 1. 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]

  • 2. 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]

  • 3. Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.
    Mukai M, Nagata E, Mizuma A, Yamano M, Sugaya K, Nishino I, Goto YI, Takizawa S.
    Intern Med; 2017 Oct 01; 56(1):95-99. PubMed ID: 28050007
    [Abstract] [Full Text] [Related]

  • 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. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun 15; 51(6):1425-8. PubMed ID: 8320824
    [Abstract] [Full Text] [Related]

  • 6. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.
    Scaglia F, Northrop JL.
    CNS Drugs; 2006 Jun 15; 20(6):443-64. PubMed ID: 16734497
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Gastro-intestinal Involvement in m.3243A>G-associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.
    Suzuki J, Iwata M, Moriyoshi H, Nishida S, Yasuda T, Ito Y.
    Intern Med; 2018 Mar 01; 57(5):771. PubMed ID: 29151541
    [No Abstract] [Full Text] [Related]

  • 9. 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 01; 40(5):405-8. PubMed ID: 11393411
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct 01; 5(5):622-32. PubMed ID: 1392136
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 12. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.
    Lahiri D, Sawale VM, Banerjee S, Dubey S, Roy BK, Das SK.
    J Med Case Rep; 2019 Mar 06; 13(1):63. PubMed ID: 30837005
    [Abstract] [Full Text] [Related]

  • 13. 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 06; 21(4):61-5. PubMed ID: 27348141
    [Abstract] [Full Text] [Related]

  • 14. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, Mariotti C, DiDonato S.
    Eur J Hum Genet; 1993 Jul 06; 1(1):80-7. PubMed ID: 8069654
    [Abstract] [Full Text] [Related]

  • 15. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K, Yamamoto M, Engel AG, Harper CM, Roberts LR, Tan GH, Fatourechi V.
    Ann Neurol; 1996 Jun 06; 39(6):761-6. PubMed ID: 8651648
    [Abstract] [Full Text] [Related]

  • 16. 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 06; 106(7):528-36. PubMed ID: 17660142
    [Abstract] [Full Text] [Related]

  • 17. Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease.
    Nikolaus M, Tietze A, Schweizer L, Kaindl AM, Stenzel W, Schuelke M, Knierim E.
    Brain Dev; 2019 Nov 06; 41(10):901-904. PubMed ID: 31345444
    [Abstract] [Full Text] [Related]

  • 18. A Caucasian family with the 3271 mutation in mitochondrial DNA.
    Marie SK, Goto Y, Passos-Bueno MR, Zatz M, Carvalho AA, Carvalho M, Levy JA, Palou VB, Campiotto S, Horai S.
    Biochem Med Metab Biol; 1994 Aug 06; 52(2):136-9. PubMed ID: 7993661
    [Abstract] [Full Text] [Related]

  • 19. Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case report.
    Mezuki S, Fukuda K, Matsushita T, Fukushima Y, Matsuo R, Goto YI, Yasukawa T, Uchiumi T, Kang D, Kitazono T, Ago T.
    BMC Neurol; 2017 Dec 13; 17(1):217. PubMed ID: 29237403
    [Abstract] [Full Text] [Related]

  • 20. Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Shoji Y, Sato W, Hayasaka K, Takada G.
    J Inherit Metab Dis; 1993 Dec 13; 16(1):27-30. PubMed ID: 8487499
    [Abstract] [Full Text] [Related]

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