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Journal Abstract Search

340 related items for PubMed ID: 19502062

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  • 2. [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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  • 8. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
    Munakata K, Iwamoto K, Bundo M, Kato T.
    Biol Psychiatry; 2005 Mar 01; 57(5):525-32. PubMed ID: 15737668
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  • 10. 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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  • 11. Population prevalence of the MELAS A3243G mutation.
    Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Mitchell P, Sue CM.
    Mitochondrion; 2007 May 18; 7(3):230-3. PubMed ID: 17300999
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  • 14. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
    Niedermayr K, Pölzl G, Scholl-Bürgi S, Fauth C, Schweigmann U, Haberlandt E, Albrecht U, Zlamy M, Sperl W, Mayr JA, Karall D.
    Congenit Heart Dis; 2018 Sep 18; 13(5):671-677. PubMed ID: 30133155
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  • 15. A mitochondrial DNA mutation in a patient with an extensive family history of Duchenne muscular dystrophy.
    Wong LJ, Wladyka C, Mardach-Verdon R.
    Muscle Nerve; 2004 Jul 18; 30(1):118-22. PubMed ID: 15221888
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  • 16. 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 18; 34(3):235-8. PubMed ID: 16504796
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  • 18. Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy.
    Di Toro A, Urtis M, Narula N, Giuliani L, Grasso M, Pasotti M, Pellegrini C, Serio A, Pilotto A, Antoniazzi E, Rampino T, Magrassi L, Valentini A, Cavallini A, Scelsi L, Ghio S, Abelli M, Olivotto I, Porcu M, Gavazzi A, Kodama T, Arbustini E.
    J Am Coll Cardiol; 2022 Oct 11; 80(15):1431-1443. PubMed ID: 36202533
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  • 19. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R, Reilmann R, Holinski-Feder E, Ringelstein EB, Klopstock T.
    Neuromuscul Disord; 2008 Jul 11; 18(7):553-6. PubMed ID: 18590963
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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 11; 9(2):115-22. PubMed ID: 19460299
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