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345 related items for PubMed ID: 2813058

  • 1. Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Nelson I, Degoul F, Obermaier-Kusser B, Romero N, Borrone C, Marsac C, Vayssiere JL, Gerbitz K, Fardeau M, Ponsot G, Lestienne P.
    Nucleic Acids Res; 1989 Oct 25; 17(20):8117-24. PubMed ID: 2813058
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S.
    N Engl J Med; 1989 May 18; 320(20):1293-9. PubMed ID: 2541333
    [Abstract] [Full Text] [Related]

  • 3. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
    Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L.
    Hum Mol Genet; 1994 Jun 18; 3(6):947-51. PubMed ID: 7951243
    [Abstract] [Full Text] [Related]

  • 4. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
    Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M.
    J Neurol Sci; 1991 Feb 18; 101(2):168-77. PubMed ID: 1851820
    [Abstract] [Full Text] [Related]

  • 5. Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome.
    Moraes CT, Schon EA, DiMauro S, Miranda AF.
    Biochem Biophys Res Commun; 1989 Apr 28; 160(2):765-71. PubMed ID: 2541710
    [Abstract] [Full Text] [Related]

  • 6. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.
    Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M.
    Pediatr Res; 1990 Aug 28; 28(2):131-6. PubMed ID: 2395603
    [Abstract] [Full Text] [Related]

  • 7. 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 Aug 28; 17(6):291-6. PubMed ID: 9832255
    [Abstract] [Full Text] [Related]

  • 8. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
    Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC.
    Proc Natl Acad Sci U S A; 1989 Oct 28; 86(20):7952-6. PubMed ID: 2554297
    [Abstract] [Full Text] [Related]

  • 9. Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
    Nakase H, Moraes CT, Rizzuto R, Lombes A, DiMauro S, Schon EA.
    Am J Hum Genet; 1990 Mar 28; 46(3):418-27. PubMed ID: 1689952
    [Abstract] [Full Text] [Related]

  • 10. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
    Gerbitz KD, Obermaier-Kusser B, Zierz S, Pongratz D, Müller-Höcker J, Lestienne P.
    J Neurol; 1990 Feb 28; 237(1):5-10. PubMed ID: 2156958
    [Abstract] [Full Text] [Related]

  • 11. 3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.
    Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen UP, Reichmann H.
    Acta Neuropathol; 1995 Feb 28; 90(2):126-9. PubMed ID: 7484086
    [Abstract] [Full Text] [Related]

  • 12. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E.
    Proc Natl Acad Sci U S A; 1989 Dec 28; 86(23):9509-13. PubMed ID: 2556715
    [Abstract] [Full Text] [Related]

  • 13. Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
    Poulton J, Morten KJ, Marchington D, Weber K, Brown GK, Rötig A, Bindoff L.
    Muscle Nerve Suppl; 1995 Dec 28; 3():S154-8. PubMed ID: 7603518
    [Abstract] [Full Text] [Related]

  • 14. Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
    Reichmann H, Degoul F, Gold R, Meurers B, Ketelsen UP, Hartmann J, Marsac C, Lestienne P.
    Eur Neurol; 1991 Dec 28; 31(2):108-13. PubMed ID: 1646110
    [Abstract] [Full Text] [Related]

  • 15. 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 Dec 28; 26 Suppl 1():162-5. PubMed ID: 8629098
    [Abstract] [Full Text] [Related]

  • 16. [Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].
    Nelson I, d'Auriol L, Galibert F, Ponsot G, Lestienne P.
    C R Acad Sci III; 1989 Dec 28; 309(10):403-7. PubMed ID: 2514965
    [Abstract] [Full Text] [Related]

  • 17. Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Shanske S, Moraes CT, Lombes A, Miranda AF, Bonilla E, Lewis P, Whelan MA, Ellsworth CA, DiMauro S.
    Neurology; 1990 Jan 28; 40(1):24-8. PubMed ID: 2296377
    [Abstract] [Full Text] [Related]

  • 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 28; 21(7):357-64. PubMed ID: 16977556
    [Abstract] [Full Text] [Related]

  • 19. Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
    Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP.
    Neurology; 1988 Sep 28; 38(9):1339-46. PubMed ID: 3412580
    [Abstract] [Full Text] [Related]

  • 20. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion.
    Lestienne P, Ponsot G.
    Lancet; 1988 Apr 16; 1(8590):885. PubMed ID: 2895391
    [No Abstract] [Full Text] [Related]

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