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Journal Abstract Search

710 related items for PubMed ID: 15857931

  • 21. Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
    Müller T, Deschauer M, Neudecker S, Zierz S.
    Acta Neuropathol; 2005 Oct; 110(4):426-30. PubMed ID: 16133542
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  • 22. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
    Zhang XA, Wu HC, Zhang BF, Yu W, Fan QS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
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  • 23. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M.
    Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426
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  • 26. Late-onset mitochondrial myopathy.
    Johnston W, Karpati G, Carpenter S, Arnold D, Shoubridge EA.
    Ann Neurol; 1995 Jan; 37(1):16-23. PubMed ID: 7818252
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  • 27. Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.
    Bidooki S, Jackson MJ, Johnson MA, Chrzanowska-Lightowlers ZM, Taylor RW, Venables G, Lightowlers RN, Turnbull DM, Bindoff LA.
    Neuromuscul Disord; 2004 Jul; 14(7):417-20. PubMed ID: 15210164
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  • 31. Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
    Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S.
    Arch Neurol; 2007 Sep; 64(9):1339-43. PubMed ID: 17846276
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  • 33. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
    Kornblum C, Zsurka G, Wiesner RJ, Schröder R, Kunz WS.
    Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
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  • 37. A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.
    Leshinsky-Silver E, Michelson M, Cohen S, Ginsberg M, Sadeh M, Barash V, Lerman-Sagie T, Lev D.
    Eur J Paediatr Neurol; 2008 Jul; 12(4):309-13. PubMed ID: 17951082
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  • 38. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.
    Eur J Med Genet; 2009 Jul; 52(1):47-8. PubMed ID: 19015050
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  • 39. [Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy].
    Li YF, Wang ZX, Gao XG, Hong DJ, Yuan Y.
    Zhonghua Yi Xue Za Zhi; 2009 Jun 16; 89(23):1593-6. PubMed ID: 19957502
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