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Journal Abstract Search

156 related items for PubMed ID: 7931425

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  • 2. MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.
    Prasad M, Narayan B, Prasad AN, Rupar CA, Levin S, Kronick J, Ramsay D, Tay KY, Prasad C.
    Can J Neurol Sci; 2014 Mar; 41(2):210-9. PubMed ID: 24534033
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  • 5. 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; 33(6):1055-61. PubMed ID: 7804130
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  • 6. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec; 156(12):1136-47. PubMed ID: 11139730
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  • 7. 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
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  • 9. 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 06; 35(3):365-70. PubMed ID: 8122891
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  • 12. Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes.
    Li W, Zhang W, Li F, Wang C.
    Int J Clin Exp Pathol; 2015 Mar 06; 8(6):7022-7. PubMed ID: 26261593
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  • 13. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 06; 51(9):2373-8. PubMed ID: 8411715
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  • 14. Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
    Morovvati S, Nakagawa M, Sato Y, Hamada K, Higuchi I, Osame M.
    Acta Neurol Scand; 2002 Aug 06; 106(2):104-8. PubMed ID: 12100370
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  • 15. 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 06; 114(2):205-8. PubMed ID: 8445402
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  • 16. Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.
    Tay SK, Shanske S, Crowe C, Shanske A, Schafer I, Pancrudo J, Lu J, Bonilla E, DiMauro S.
    J Child Neurol; 2005 Feb 06; 20(2):142-6. PubMed ID: 15794182
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  • 19. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar 06; 34(3):235-8. PubMed ID: 16504796
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