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Journal Abstract Search

678 related items for PubMed ID: 2541333

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  • 23. [Partial deletion of mitochondrial DNA in mitochondrial encephalomyopathies].
    Wang W, Zhang J, Guo Y, Guo Z, Ren H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug; 19(4):278-83. PubMed ID: 10453567
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  • 27. 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; 29(6):680-3. PubMed ID: 1892371
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  • 28. Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?
    Moraes CT, Zeviani M, Schon EA, Hickman RO, Vlcek BW, DiMauro S.
    Am J Med Genet; 1991 Dec 01; 41(3):301-5. PubMed ID: 1789283
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  • 29. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome].
    Soga F, Ueno S, Yorifuji S.
    Nihon Rinsho; 1993 Sep 01; 51(9):2386-90. PubMed ID: 8411717
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  • 30. 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 01; 46(3):418-27. PubMed ID: 1689952
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  • 31. [A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].
    Akaike M, Kawai H, Kashiwagi S, Kunishige M, Saito S.
    Rinsho Shinkeigaku; 1995 Feb 01; 35(2):190-4. PubMed ID: 7781238
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  • 32. Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies.
    Mitsui T, Kawai H, Nagasawa M, Kunishige M, Akaike M, Kimura Y, Saito S.
    J Neurol Sci; 1996 Jul 01; 139(1):111-6. PubMed ID: 8836981
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  • 33. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
    Mol Genet Genomic Med; 2024 Jan 01; 12(1):e2328. PubMed ID: 38018320
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  • 34. [Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA].
    Tanno Y, Yoneda M, Ohnishi Y, Miyatake T, Ozawa T.
    Rinsho Shinkeigaku; 1989 Sep 01; 29(9):1176-9. PubMed ID: 2598547
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  • 35. [Expression of a defect in the respiratory chain in cultured human cells].
    Meola G, Rotondo G, Velicogna M, Toppi R, Sansone V, Bresolin N, Comi G, Bordoni A, Amati P, Ausenda C.
    Riv Neurol; 1991 Sep 01; 61(4):122-34. PubMed ID: 1667713
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  • 36. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
    Tabaku M, Legius E, Robberecht W, Sciot R, Fryns JP, Cassiman JJ, Matthijs G.
    Genet Couns; 1999 Sep 01; 10(3):285-93. PubMed ID: 10546101
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  • 37. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
    Ernst BP, Wilichowski E, Wagner M, Hanefeld F.
    Mol Cell Probes; 1994 Feb 01; 8(1):45-9. PubMed ID: 8028607
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  • 38. [Chronic progressive external ophthalmoplegia--symptom or syndrome?].
    Bau V, Deschauer M, Zierz S.
    Klin Monbl Augenheilkd; 2009 Oct 01; 226(10):822-8. PubMed ID: 19830638
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  • 39. 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 01; 90(1):61-6. PubMed ID: 1634620
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  • 40. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ, Cruz-Martínez A, Campos-González Y, Gutiérrez-Molina M, Santiago-Pérez S, Pérez-Conde MC, López-Pajares MR, Martín-Casarrubias MA, Rubio-Muñoz JC, del Hoyo P, Arpa-Fernández A, Arenas-Barbero J.
    Rev Neurol; 1992 Jul 01; 41(8):449-54. PubMed ID: 16224730
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