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Journal Abstract Search

182 related items for PubMed ID: 15493224

  • 1. [Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].
    Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B.
    Orv Hetil; 2004 Aug 29; 145(35):1805-9. PubMed ID: 15493224
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  • 5. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ.
    Brain Dev; 2004 Oct 29; 26(7):459-62. PubMed ID: 15351082
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  • 6. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar 29; 34(3):235-8. PubMed ID: 16504796
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  • 9. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.
    Connolly BS, Feigenbaum AS, Robinson BH, Dipchand AI, Simon DK, Tarnopolsky MA.
    Biochem Biophys Res Commun; 2010 Nov 12; 402(2):443-7. PubMed ID: 20965148
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  • 10. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].
    Pérez López-Fraile MI, Barrena R, Montoya J, Marta E.
    Neurologia; 2006 Nov 12; 21(6):327-32. PubMed ID: 16799910
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  • 11. A novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS.
    Menotti F, Brega A, Diegoli M, Grasso M, Modena MG, Arbustini E.
    Ital Heart J; 2004 Jun 12; 5(6):460-5. PubMed ID: 15320572
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  • 12. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; 2004 Jun 12; 33(2):148-50. PubMed ID: 11562875
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  • 15. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M, Szczuciński A, Losy J.
    Neurol Neurochir Pol; 2014 Jun 12; 48(2):150-3. PubMed ID: 24821643
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  • 16. [Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].
    Ma YN, Fang F, Yang YL, Zhang Y, Wang ST, Xu YF, Pei P, Yuan Y, Bu DF, Qi Y.
    Zhonghua Yi Xue Za Zhi; 2008 Dec 16; 88(46):3250-3. PubMed ID: 19159547
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  • 17. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb 16; 27(1):77-80. PubMed ID: 15782498
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  • 18. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
    Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L.
    Clin Neuropathol; 2002 Feb 16; 21(2):72-6. PubMed ID: 12005255
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  • 19. A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance.
    Martin-Kleiner I, Pape-Medvidović E, Pavlić-Renar I, Metelko Z, Kusec R, Gabrilovac J, Boranić M.
    Acta Diabetol; 2004 Dec 16; 41(4):179-84. PubMed ID: 15660201
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  • 20. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
    Mimaki M, Hatakeyama H, Ichiyama T, Isumi H, Furukawa S, Akasaka M, Kamei A, Komaki H, Nishino I, Nonaka I, Goto Y.
    Mitochondrion; 2009 Apr 16; 9(2):115-22. PubMed ID: 19460299
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