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Journal Abstract Search

279 related items for PubMed ID: 10660156

  • 1. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW, Huang CC, Tsai JL, Liu JY, Pang CY, Lee HC, Wang EK, Wei YH.
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
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  • 3. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.
    Wang Z, Liu S, Yang Y, Yuan Y, Wu L, Qi Y, Chen Q.
    Chin Med J (Engl); 2002 Jul; 115(7):995-7. PubMed ID: 12150728
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  • 4. [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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  • 5. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K, Yamamoto M, Engel AG, Harper CM, Roberts LR, Tan GH, Fatourechi V.
    Ann Neurol; 1996 Jun 16; 39(6):761-6. PubMed ID: 8651648
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  • 6. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R, Zárate-Moysen A, Monsalvo-Reyes A, Herrero MD, Ruiz-Pesini E, López-Pérez M, Montoya J, Montiel-Sosa JF.
    Rev Neurol; 1996 Jun 16; 44(1):18-22. PubMed ID: 17199225
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  • 7. [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 Jun 16; 21(6):327-32. PubMed ID: 16799910
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  • 8. 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 16; 5(6):460-5. PubMed ID: 15320572
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  • 9. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
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  • 10. 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 13; 34(3):235-8. PubMed ID: 16504796
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  • 11. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ.
    Brain Dev; 2004 Oct 13; 26(7):459-62. PubMed ID: 15351082
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  • 13. Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree.
    Dubeau F, De Stefano N, Zifkin BG, Arnold DL, Shoubridge EA.
    Ann Neurol; 2000 Feb 13; 47(2):179-85. PubMed ID: 10665488
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  • 14. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec 13; 156(12):1136-47. PubMed ID: 11139730
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  • 16. 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 13; 30(1):118-22. PubMed ID: 15221888
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  • 20. Clinical features of MELAS and its relation with A3243G gene point mutation.
    Zhang J, Guo J, Fang W, Jun Q, Shi K.
    Int J Clin Exp Pathol; 2015 Jul 13; 8(10):13411-5. PubMed ID: 26722549
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