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PUBMED FOR HANDHELDS

Journal Abstract Search


238 related items for PubMed ID: 8008000

  • 21. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.
    Suomalainen A, Majander A, Haltia M, Somer H, Lönnqvist J, Savontaus ML, Peltonen L.
    J Clin Invest; 1992 Jul; 90(1):61-6. PubMed ID: 1634620
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  • 23. Multiple deletions in mitochondrial DNA are present in senescent mouse brain.
    Brossas JY, Barreau E, Courtois Y, Tréton J.
    Biochem Biophys Res Commun; 1994 Jul 29; 202(2):654-9. PubMed ID: 8048933
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  • 25. Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother.
    Casademont J, Barrientos A, Cardellach F, Rötig A, Grau JM, Montoya J, Beltrán B, Cervantes F, Rozman C, Estivill X.
    Hum Mol Genet; 1994 Nov 29; 3(11):1945-9. PubMed ID: 7874110
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  • 26. Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.
    Barthélémy C, Ogier de Baulny H, Diaz J, Cheval MA, Frachon P, Romero N, Goutieres F, Fardeau M, Lombès A.
    Ann Neurol; 2001 May 29; 49(5):607-17. PubMed ID: 11357951
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  • 27. Multiple skeletal muscle mitochondrial DNA deletions in patients with unilateral peripheral arterial disease.
    Brass EP, Wang H, Hiatt WR.
    Vasc Med; 2000 May 29; 5(4):225-30. PubMed ID: 11213234
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  • 29. Ocular myopathy and mitochondrial DNA deletion. A presentation of seven identified Danish patients.
    Magalhães PJ, Sjö O, Nørby S.
    Acta Ophthalmol Scand Suppl; 1996 May 29; (219):29-32. PubMed ID: 8741113
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  • 30. Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.
    Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S.
    Ann Neurol; 1996 Jun 29; 39(6):789-95. PubMed ID: 8651651
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  • 31. Detection of deletions flanked by short direct repeats in mitochondrial DNA of aging Drosophila.
    Yui R, Matsuura ET.
    Mutat Res; 2006 Feb 22; 594(1-2):155-61. PubMed ID: 16289600
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  • 36. Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-de Lange phenotype.
    Melegh B, Bock I, Gáti I, Méhes K.
    Am J Med Genet; 1996 Oct 02; 65(1):82-8. PubMed ID: 8914746
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  • 38. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
    Filosto M, Mancuso M, Vives-Bauza C, Vilà MR, Shanske S, Hirano M, Andreu AL, DiMauro S.
    Ann Neurol; 2003 Oct 02; 54(4):524-6. PubMed ID: 14520667
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