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Journal Abstract Search

280 related items for PubMed ID: 17223431

  • 1.
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  • 2. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
    Kärppä M, Mahjneh I, Karttunen A, Tolonen U, Majamaa K.
    J Neurol; 2004 May; 251(5):556-63. PubMed ID: 15164188
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  • 4. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K.
    Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
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  • 5. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
    Janssen AJ, Schuelke M, Smeitink JA, Trijbels FJ, Sengers RC, Lucke B, Wintjes LT, Morava E, van Engelen BG, Smits BW, Hol FA, Siers MH, Ter Laak H, van der Knaap MS, Van Spronsen FJ, Rodenburg RJ, van den Heuvel LP.
    Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232
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  • 6. [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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  • 7. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
    Marotta R, Reardon K, McKelvie PA, Chiotis M, Chin J, Cook M, Collins SJ.
    J Clin Neurosci; 2009 Sep 16; 16(9):1223-5. PubMed ID: 19502062
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  • 10. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May 16; 113(5):334-41. PubMed ID: 16629770
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  • 11. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov 16; 110(11):851-5. PubMed ID: 9772417
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  • 12. Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A > G tRNA(Leu) mutation.
    van Eijsden RG, Eijssen LM, Lindsey PJ, van den Burg CM, de Wit LE, Rubio-Gozalbo ME, de Die CE, Ayoubi T, Sluiter W, de Coo IF, Smeets HJ.
    J Med Genet; 2008 Aug 16; 45(8):525-34. PubMed ID: 18456717
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  • 14. Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.
    Florian A, Ludwig A, Stubbe-Dräger B, Boentert M, Young P, Waltenberger J, Rösch S, Sechtem U, Yilmaz A.
    J Cardiovasc Magn Reson; 2015 May 22; 17(1):40. PubMed ID: 26001801
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  • 15. Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
    Santorelli FM, Tanji K, Kulikova R, Shanske S, Vilarinho L, Hays AP, DiMauro S.
    Biochem Biophys Res Commun; 1997 Sep 18; 238(2):326-8. PubMed ID: 9299505
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  • 16. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep 18; 4(5):631-44. PubMed ID: 15347257
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  • 17. Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
    Liolitsa D, Rahman S, Benton S, Carr LJ, Hanna MG.
    Ann Neurol; 2003 Jan 18; 53(1):128-32. PubMed ID: 12509858
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  • 18. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov 18; 122(11):978-81. PubMed ID: 9822126
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  • 19. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC.
    Arch Neurol; 2007 Nov 18; 64(11):1625-7. PubMed ID: 17998445
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