These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

180 related items for PubMed ID: 9243242

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA.
    Lin CM, Thajeb P.
    Metab Brain Dis; 2007 Mar; 22(1):105-9. PubMed ID: 17226098
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 Mar 06; 56(1):95-99. PubMed ID: 28050007
    [Abstract] [Full Text] [Related]

  • 6. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Fukuda M, Nagao Y.
    J Med Case Rep; 2019 Oct 21; 13(1):313. PubMed ID: 31630688
    [Abstract] [Full Text] [Related]

  • 7. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W, Hayasaka K, Shoji Y, Takahashi T, Takada G, Saito M, Fukawa O, Wachi E.
    Biochem Mol Biol Int; 1994 Aug 21; 33(6):1055-61. PubMed ID: 7804130
    [Abstract] [Full Text] [Related]

  • 8. [MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes].
    Mierzewska H, Mroczek K, Pronicki M, Pronicka E, Karczmarewicz E, Bartnik E, Zdzienicka E, Seniów J, Schmidt-Sidor B, Taraszewska A, Palasik W.
    Neurol Neurochir Pol; 2002 Aug 21; 36(3):457-70. PubMed ID: 12185802
    [Abstract] [Full Text] [Related]

  • 9. A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob disease.
    Isozumi K, Fukuuchi Y, Tanaka K, Nogawa S, Ishihara T, Sakuta R.
    Intern Med; 1994 Sep 21; 33(9):543-6. PubMed ID: 8000105
    [Abstract] [Full Text] [Related]

  • 10. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.
    Scaglia F, Northrop JL.
    CNS Drugs; 2006 Sep 21; 20(6):443-64. PubMed ID: 16734497
    [Abstract] [Full Text] [Related]

  • 11. 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 21; 35(3):365-70. PubMed ID: 8122891
    [Abstract] [Full Text] [Related]

  • 12. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 21; 51(9):2373-8. PubMed ID: 8411715
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study.
    Onishi H, Inoue K, Osaka H, Kimura S, Nagatomo H, Hanihara T, Kawamoto S, Okuda K, Yamada Y, Kosaka K.
    J Neurol Sci; 1993 Feb 21; 114(2):205-8. PubMed ID: 8445402
    [Abstract] [Full Text] [Related]

  • 14. MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene.
    Kuwajima M, Goto M, Kurane K, Shimbo H, Omika N, Jimbo EF, Muramatsu K, Tajika M, Shimura M, Murayama K, Kurosawa K, Yamagata T, Osaka H.
    Brain Dev; 2019 May 21; 41(5):465-469. PubMed ID: 30739820
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with deterioration during pregnancy.
    Yanagawa T, Sakaguchi H, Nakao T, Sasaki H, Matsumoto G, Sanke T, Nanjo K.
    Intern Med; 1998 Sep 21; 37(9):780-3. PubMed ID: 9804089
    [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 21; 106(7):528-36. PubMed ID: 17660142
    [Abstract] [Full Text] [Related]

  • 17. Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy.
    Chiyonobu T, Noda R, Yoshida M, Fujiki A, Ishii R, Nukina S, Fujita K, Goto Y, Morimoto M.
    Brain Dev; 2008 Jun 21; 30(6):430-3. PubMed ID: 18226864
    [Abstract] [Full Text] [Related]

  • 18. A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS.
    Shin HJ, Na JH, Lee YM.
    Neurol Sci; 2024 May 21; 45(5):2337-2339. PubMed ID: 38265537
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. The 3243 MELAS mutation in a pedigree with MERRF.
    Folgerø T, Torbergsen T, Oian P.
    Eur Neurol; 1995 Oct 01; 35(3):168-71. PubMed ID: 7628497
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.