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166 related items for PubMed ID: 1334946

  • 1. In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy.
    Müller-Höcker J, Seibel P, Schneiderbanger K, Zietz C, Obermaier-Kusser B, Gerbitz KD, Kadenbach B.
    Hum Pathol; 1992 Dec; 23(12):1431-7. PubMed ID: 1334946
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  • 2. The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome.
    Müller-Höcker J, Jacob U, Seibel P.
    Mod Pathol; 1998 Mar; 11(3):295-301. PubMed ID: 9521479
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  • 3. 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; 86(23):9509-13. PubMed ID: 2556715
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  • 4. Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe.
    Nakamura N, Hattori N, Tanaka M, Mizuno Y.
    Biochim Biophys Acta; 1996 Sep 11; 1308(3):215-21. PubMed ID: 8809113
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  • 5. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul 11; 110(1-2):169-77. PubMed ID: 1324295
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  • 6. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome].
    Soga F, Ueno S, Yorifuji S.
    Nihon Rinsho; 1993 Sep 11; 51(9):2386-90. PubMed ID: 8411717
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  • 7. Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection.
    Pistilli D, di Gioia CR, D'Amati G, Sciacchitano S, Quaglione R, Quitadamo R, Casali C, Gallo P, Santorelli FM.
    Hum Pathol; 2003 Oct 11; 34(10):1058-61. PubMed ID: 14608542
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  • 9. Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.
    Moraes CT, Ricci E, Petruzzella V, Shanske S, DiMauro S, Schon EA, Bonilla E.
    Nat Genet; 1992 Aug 11; 1(5):359-67. PubMed ID: 1284549
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  • 10. Loss of myelin-associated glycoprotein in kearns-sayre syndrome.
    Lax NZ, Campbell GR, Reeve AK, Ohno N, Zambonin J, Blakely EL, Taylor RW, Bonilla E, Tanji K, DiMauro S, Jaros E, Lassmann H, Turnbull DM, Mahad DJ.
    Arch Neurol; 2012 Apr 11; 69(4):490-9. PubMed ID: 22491194
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  • 13. 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
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  • 15. 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
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  • 18. 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 Oct 28; 17(6):291-6. PubMed ID: 9832255
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