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Journal Abstract Search

178 related items for PubMed ID: 8026131

  • 1. [Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene].
    Hara K, Yamamoto M, Anegawa T, Sakuta R, Nakamura M.
    Rinsho Shinkeigaku; 1994 Apr; 34(4):361-5. PubMed ID: 8026131
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  • 2. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T, Kawarai T, Watanabe C, Katayama S, Nakamura S.
    No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
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  • 4. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
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  • 6. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar; 44(3):259-64. PubMed ID: 1591103
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  • 8. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
    Kawakami Y, Sakuta R, Hashimoto K, Fujino O, Fujita T, Hida M, Horai S, Goto Y, Nonaka I.
    Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
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  • 9. Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Hutchison WM, Thyagarajan D, Poulton J, Marchington DR, Kirby DM, Manji SS, Dahl HH.
    Arch Neurol; 2005 Dec; 62(12):1920-3. PubMed ID: 16344351
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  • 19. Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
    Pereira C, Nogueira C, Barbot C, Tessa A, Soares C, Fattori F, Guimarães A, Santorelli FM, Vilarinho L.
    Biochem Biophys Res Commun; 2007 Mar 23; 354(4):937-41. PubMed ID: 17266923
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  • 20. [Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy].
    Franco E, Bautista J, Luque R, Chinchón I, García-Lozano R, Aguilera I, Campos Y, Arenas J.
    Neurologia; 1999 Nov 23; 14(9):463-6. PubMed ID: 10613022
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