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Journal Abstract Search

539 related items for PubMed ID: 16977556

  • 1. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ, Lopez Gallardo E, Solano A, Dahmani Y, Herrero MD, Montoya J.
    Neurologia; 2006 Sep; 21(7):357-64. PubMed ID: 16977556
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  • 3. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
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  • 4. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome].
    Soga F, Ueno S, Yorifuji S.
    Nihon Rinsho; 1993 Sep; 51(9):2386-90. PubMed ID: 8411717
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  • 5. Mitochondrial genome analysis in Kearns-Sayre syndrome.
    Lertrit P, Atchaneeyasakul L, Devahastin V, Saechan V, Sangruchi T, Neungton N, Lekhakula S.
    Southeast Asian J Trop Med Public Health; 1995 Sep; 26 Suppl 1():162-5. PubMed ID: 8629098
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  • 7. 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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  • 9. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S, Molnar M, Buse G, Schröder JM.
    Clin Neuropathol; 1998 Nov; 17(6):291-6. PubMed ID: 9832255
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  • 11. [Chronic progressive external ophthalmoplegia (CPEO); mitochondrial DNA deletion, brain MRI and electrophysiological studies].
    Nakagawa M, Tokimura M, Kuriyama M, Higuchi I, Osame M.
    Rinsho Shinkeigaku; 1991 Sep; 31(9):981-6. PubMed ID: 1769162
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  • 12. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
    Ernst BP, Wilichowski E, Wagner M, Hanefeld F.
    Mol Cell Probes; 1994 Feb; 8(1):45-9. PubMed ID: 8028607
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  • 13. Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population.
    Remes AM, Majamaa-Voltti K, Kärppä M, Moilanen JS, Uimonen S, Helander H, Rusanen H, Salmela PI, Sorri M, Hassinen IE, Majamaa K.
    Neurology; 2005 Mar 22; 64(6):976-81. PubMed ID: 15781811
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  • 14. Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA.
    Zoccolella S, Torraco A, Amati A, Lamberti P, Serlenga L, Papa S, Petruzzella V.
    Funct Neurol; 2006 Mar 22; 21(1):39-41. PubMed ID: 16735000
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  • 15. The neurological evolution of Pearson syndrome: case report and literature review.
    Lee HF, Lee HJ, Chi CS, Tsai CR, Chang TK, Wang CJ.
    Eur J Paediatr Neurol; 2007 Jul 22; 11(4):208-14. PubMed ID: 17434771
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  • 16. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H, Sugimura T, Yamada T, Hayashi K, Kobayashi T.
    Rinsho Shinkeigaku; 1997 Aug 22; 37(8):680-4. PubMed ID: 9404143
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  • 17. Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.
    Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S.
    Ann Neurol; 1990 Jul 22; 28(1):94-7. PubMed ID: 2375642
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  • 18. [A case of Kearns-Sayre syndrome].
    Kokot W, Iwaszkiewicz-Bilikiewiczowa B, Lewczuk A, Sworczak K.
    Klin Oczna; 1996 Jul 22; 98(4):327-30. PubMed ID: 9463130
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  • 20. [Mitochondrial disease and complete heart block. Kearns-Sayre syndrome. Description of a case].
    Perocchio M, Tomassini B, Biasia R, Belli Valletta M, Cerutti A, Bobba F.
    Minerva Med; 1992 Dec 22; 83(12 Suppl 1):7-13. PubMed ID: 1300476
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