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Journal Abstract Search

123 related items for PubMed ID: 7980504

  • 21. Oxidative capacity correlates with muscle mutation load in mitochondrial myopathy.
    Jeppesen TD, Schwartz M, Olsen DB, Vissing J.
    Ann Neurol; 2003 Jul; 54(1):86-92. PubMed ID: 12838523
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  • 22. Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA.
    Thajeb P, Ma YS, Tzen CY, Chuang CK, Wu TY, Chen SC, Wei YH.
    Clin Neurol Neurosurg; 2006 Jun; 108(4):407-10. PubMed ID: 16644408
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  • 27. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
    Moslemi AR, Melberg A, Holme E, Oldfors A.
    Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
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  • 28. Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G-->A mitochondrial DNA mutation.
    Spinazzola A, Carrara F, Mora M, Zeviani M.
    Neuromuscul Disord; 2004 Dec; 14(12):815-7. PubMed ID: 15564038
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  • 29. Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO).
    Hattori Y, Goto Y, Sakuta R, Nonaka I, Mizuno Y, Horai S.
    J Neurol Sci; 1994 Aug; 125(1):50-5. PubMed ID: 7525879
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  • 31. A novel mitochondrial tRNA(Phe) mutation inhibiting anticodon stem formation associated with a muscle disease.
    Kleinle S, Schneider V, Moosmann P, Brandner S, Krähenbühl S, Liechti-Gallati S.
    Biochem Biophys Res Commun; 1998 Jun 09; 247(1):112-5. PubMed ID: 9636664
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  • 33. A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia.
    Spagnolo M, Tomelleri G, Vattemi G, Filosto M, Rizzuto N, Tonin P.
    Neuromuscul Disord; 2001 Jul 09; 11(5):481-4. PubMed ID: 11404121
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  • 37. A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia.
    Souilem S, Chebel S, Mancuso M, Petrozzi L, Siciliano G, FrihAyed M, Hentati F, Amouri R.
    J Neurol Sci; 2011 Jan 15; 300(1-2):187-90. PubMed ID: 20884012
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  • 39. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
    Sawano T, Tanaka M, Ohno K, Yoneda M, Ota Y, Terasaki H, Awaya S, Ozawa T.
    Biochem Mol Biol Int; 1996 Apr 15; 38(4):693-700. PubMed ID: 8728098
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  • 40. [Molecular studies in Cuban patients with progressive external ophthalmoplegia].
    Rodríguez-Hernández M, Hirano M, Arrieta T, Lestayo Z, Estrada R, Santiesteban R, Guerra-Badía R, Galarraga J, Gutierres J, Hechevarría E, Andreu A, Montoya J, DiMauro S.
    Rev Neurol; 1996 Apr 15; 30(11):1001-5. PubMed ID: 10904941
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