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Journal Abstract Search

165 related items for PubMed ID: 8836308

  • 1. MELAS syndrome associated with a tandem duplication in the D-loop of mitochondrial DNA.
    Li JY, Kong KW, Chang MH, Cheung SC, Lee HC, Pang CY, Wei YH.
    Acta Neurol Scand; 1996 Jun; 93(6):450-5. PubMed ID: 8836308
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  • 2. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.
    Hsieh RH, Li JY, Pang CY, Wei YH.
    J Biomed Sci; 2001 Jun; 8(4):328-35. PubMed ID: 11455195
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  • 3. 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; 106(7):528-36. PubMed ID: 17660142
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  • 4. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
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  • 5. 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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  • 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; 2000 Jan; 44(1):18-22. PubMed ID: 17199225
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  • 7. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
    Fabrizi GM, Cardaioli E, Grieco GS, Cavallaro T, Malandrini A, Manneschi L, Dotti MT, Federico A, Guazzi G.
    J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
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  • 8. Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes.
    Li W, Zhang W, Li F, Wang C.
    Int J Clin Exp Pathol; 2015 Jul; 8(6):7022-7. PubMed ID: 26261593
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  • 10. 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; 8(10):13411-5. PubMed ID: 26722549
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  • 11. 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; 39(6):761-6. PubMed ID: 8651648
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  • 14. Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
    Morovvati S, Nakagawa M, Sato Y, Hamada K, Higuchi I, Osame M.
    Acta Neurol Scand; 2002 Aug; 106(2):104-8. PubMed ID: 12100370
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  • 18. 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; 19(2):187-90. PubMed ID: 8559168
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