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Journal Abstract Search

244 related items for PubMed ID: 15794182

  • 1.
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  • 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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  • 5. A juvenile case of MELAS with T3271C mitochondrial DNA mutation.
    Stenqvist L, Paetau A, Valanne L, Suomalainen A, Pihko H.
    Pediatr Res; 2005 Aug; 58(2):258-62. PubMed ID: 16006433
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  • 6. 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 Aug; 8(10):13411-5. PubMed ID: 26722549
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  • 7. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R.
    Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777
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  • 10. A boy with muscle weakness, hypercarbia, and the mitochondrial DNA A3243G mutation.
    Saneto RP, Bouldin A.
    J Child Neurol; 2006 Jan; 21(1):77-9. PubMed ID: 16551459
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  • 11. [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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  • 12. Clinical and genetic features in a MELAS child with a 3271T>C mutation.
    Chou HF, Liang WC, Zhang Q, Goto Y, Jong YJ.
    Pediatr Neurol; 2008 Feb 29; 38(2):143-6. PubMed ID: 18206799
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  • 13. [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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  • 14. Clinical, physiological, and histological features in a kindred with the T3271C melas mutation.
    Tarnopolsky MA, Maguire J, Myint T, Applegarth D, Robinson BH.
    Muscle Nerve; 1998 Jan 16; 21(1):25-33. PubMed ID: 9427220
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  • 16. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.
    Li JY, Hsieh RH, Peng NJ, Lai PH, Lee CF, Lo YK, Wei YH.
    J Formos Med Assoc; 2007 Jul 16; 106(7):528-36. PubMed ID: 17660142
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  • 17. Screening for MELAS mutations in young patients with stroke of undetermined origin.
    Conforto AB, Yamamoto FI, Oba-Shinjo SM, Pinto JG, Hoshino M, Scaff M, Marie SK.
    Arq Neuropsiquiatr; 2007 Jun 16; 65(2B):371-6. PubMed ID: 17664998
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  • 18. Infantile encephalopathy associated with the MELAS A3243G mutation.
    Sue CM, Bruno C, Andreu AL, Cargan A, Mendell JR, Tsao CY, Luquette M, Paolicchi J, Shanske S, DiMauro S, De Vivo DC.
    J Pediatr; 1999 Jun 16; 134(6):696-700. PubMed ID: 10356136
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  • 19. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J.
    Muscle Nerve; 1996 Feb 16; 19(2):187-90. PubMed ID: 8559168
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  • 20. ["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 16; 156(12):1136-47. PubMed ID: 11139730
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