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Journal Abstract Search

596 related items for PubMed ID: 7684581

  • 21. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.
    Cevoli S, Pallotti F, La Morgia C, Valentino ML, Pierangeli G, Cortelli P, Baruzzi A, Montagna P, Carelli V.
    Cephalalgia; 2010 Aug; 30(8):919-27. PubMed ID: 20656703
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  • 24. An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
    Ravn K, Wibrand F, Hansen FJ, Horn N, Rosenberg T, Schwartz M.
    Eur J Hum Genet; 2001 Oct; 9(10):805-9. PubMed ID: 11781695
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  • 25. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
    Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T.
    Proc Natl Acad Sci U S A; 2005 May 17; 102(20):7127-32. PubMed ID: 15870203
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  • 29. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency].
    Sumi K, Nagaura T, Itagaki Y, Inui K, Abe J.
    Rinsho Shinkeigaku; 1989 Jul 17; 29(7):901-8. PubMed ID: 2553313
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  • 30. [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 17; 50(12):1089-92. PubMed ID: 9989353
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  • 31. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov 17; 122(11):978-81. PubMed ID: 9822126
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  • 32. Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.
    Mita S, Tokunaga M, Kumamoto T, Uchino M, Nonaka I, Ando M.
    Muscle Nerve Suppl; 1995 Nov 17; 3():S113-8. PubMed ID: 7603511
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  • 36. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun 17; 29(6):680-3. PubMed ID: 1892371
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  • 37. Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathy.
    Kovalenko SA, Tanaka M, Yoneda M, Iakovlev AF, Ozawa T.
    Biochem Biophys Res Commun; 1996 May 15; 222(2):201-7. PubMed ID: 8670183
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  • 38. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE.
    Brain; 1995 Jun 15; 118 ( Pt 3)():721-34. PubMed ID: 7600089
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  • 39. Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243.
    Petruzzella V, Moraes CT, Sano MC, Bonilla E, DiMauro S, Schon EA.
    Hum Mol Genet; 1994 Mar 15; 3(3):449-54. PubMed ID: 7912129
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  • 40. Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.
    Tanno Y, Yoneda M, Tanaka K, Tanaka H, Yamazaki M, Nishizawa M, Wakabayashi K, Ohama E, Tsuji S.
    Muscle Nerve; 1995 Dec 15; 18(12):1390-7. PubMed ID: 7477061
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