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Journal Abstract Search

136 related items for PubMed ID: 8186712

  • 1. Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion.
    Tranchant C, Mousson B, Mohr M, Dumoulin R, Welsch M, Weess C, Stepien G, Warter JM.
    Neuromuscul Disord; 1993; 3(5-6):561-6. PubMed ID: 8186712
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  • 4. Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome.
    Kleber FX, Park JW, Hübner G, Johannes A, Pongratz D, König E.
    Klin Wochenschr; 1987 May 15; 65(10):480-6. PubMed ID: 3599796
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  • 5. Mitochondrial DNA deletion diagnosed by analysis of an endomyocardial biopsy specimen from a patient with Kearns-Sayre syndrome and complete heart block.
    Remes AM, Hassinen IE, Majamaa K, Peuhkurinen KJ.
    Br Heart J; 1992 Oct 15; 68(4):408-11. PubMed ID: 1449926
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  • 6. Deletion of mitochondrial DNA in the endomyocardial biopsy sample from a patient with Kearns-Sayre syndrome.
    Anan R, Nakagawa M, Higuchi I, Nakao S, Nomoto K, Tanaka H.
    Eur Heart J; 1992 Dec 15; 13(12):1718-9. PubMed ID: 1289103
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  • 8. A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples.
    De Coo IF, Gussinklo T, Arts PJ, Van Oost BA, Smeets HJ.
    J Neurol Sci; 1997 Jul 15; 149(1):37-40. PubMed ID: 9168163
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  • 9. 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 Jul 15; 26 Suppl 1():162-5. PubMed ID: 8629098
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  • 10. 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 15; 23(12):1431-7. PubMed ID: 1334946
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  • 11. High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heart.
    Fromenty B, Carrozzo R, Shanske S, Schon EA.
    Am J Med Genet; 1997 Sep 05; 71(4):443-52. PubMed ID: 9286453
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  • 12. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun 05; 29(6):680-3. PubMed ID: 1892371
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  • 14. 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
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  • 15. Kearns-Sayre syndrome "plus". Classical clinical findings and dystonia.
    Marie SK, Carvalho AA, Fonseca LF, Carvalho MS, Reed UC, Scaff M.
    Arq Neuropsiquiatr; 1999 Dec 25; 57(4):1017-23. PubMed ID: 10683696
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  • 17. A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment.
    Obara-Moszynska M, Maceluch J, Bobkowski W, Baszko A, Jaremba O, Krawczynski MR, Niedziela M.
    BMC Pediatr; 2013 Feb 20; 13():27. PubMed ID: 23421922
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  • 18. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A, Casademont J, Grau JM, Cardellach F, Montoya J, Estivill X, Urbano-Márquez A, Nunes V.
    Med Clin (Barc); 1995 Jul 01; 105(5):180-4. PubMed ID: 7630231
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  • 20. A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.
    Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R.
    Arch Neurol; 2001 Jul 01; 58(7):1113-8. PubMed ID: 11448301
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