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Journal Abstract Search

238 related items for PubMed ID: 8008000

  • 1. Widespread tissue distribution of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Kawashima S, Ohta S, Kagawa Y, Yoshida M, Nishizawa M.
    Muscle Nerve; 1994 Jul; 17(7):741-6. PubMed ID: 8008000
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  • 2. 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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  • 4. Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia.
    Ville-Ferlin T, Dumoulin R, Stepien G, Matha V, Bady B, Flocard F, Carrier H, Mathieu M, Mousson B.
    Mol Cell Probes; 1995 Jun; 9(3):207-14. PubMed ID: 7477015
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  • 7. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K, Yamamoto M, Engel AG, Harper CM, Roberts LR, Tan GH, Fatourechi V.
    Ann Neurol; 1996 Jun; 39(6):761-6. PubMed ID: 8651648
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  • 8. Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood.
    Houshmand M, Gardner A, Hällström T, Müntzing K, Oldfors A, Holme E.
    Neuromuscul Disord; 2004 Mar; 14(3):195-201. PubMed ID: 15036329
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  • 9. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
    Di Fonzo A, Bordoni A, Crimi M, Sara G, Del Bo R, Bresolin N, Comi GP.
    Hum Mutat; 2003 Dec; 22(6):498-9. PubMed ID: 14635118
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  • 11. Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions.
    Paul R, Desnuelle C, Pouget J, Pellissier JF, Richelme C, Monfort MF, Butori C, Saunieres A, Paquis-Flucklinger V.
    Eur J Hum Genet; 2000 May; 8(5):331-8. PubMed ID: 10854092
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  • 15. Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Nishizuka S, Tamura G, Goto Y, Murayama K, Konno T, Hakozaki M, Nonaka I, Tohgi H, Satodate R.
    Biochem Biophys Res Commun; 1998 Jun 09; 247(1):24-7. PubMed ID: 9636647
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  • 16. A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.
    Leshinsky-Silver E, Michelson M, Cohen S, Ginsberg M, Sadeh M, Barash V, Lerman-Sagie T, Lev D.
    Eur J Paediatr Neurol; 2008 Jul 09; 12(4):309-13. PubMed ID: 17951082
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  • 17. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
    Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S, DiDonato S.
    Nature; 1989 May 25; 339(6222):309-11. PubMed ID: 2725645
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  • 18. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep 25; 21(7):357-64. PubMed ID: 16977556
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  • 19. No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations.
    Schwartz M, Vissing J.
    J Neurol Sci; 2004 Mar 15; 218(1-2):99-101. PubMed ID: 14759640
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  • 20. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.
    Brockington M, Sweeney MG, Hammans SR, Morgan-Hughes JA, Harding AE.
    Nat Genet; 1993 May 15; 4(1):67-71. PubMed ID: 8513327
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