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Journal Abstract Search

285 related items for PubMed ID: 20799154

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  • 2. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL, Bao XH, Ma YN, Chang XZ, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):130-5. PubMed ID: 23527980
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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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  • 5. 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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  • 7. Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.
    Tzoulis C, Bindoff LA.
    Stroke; 2009 Feb; 40(2):e15-7. PubMed ID: 19095975
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  • 12. A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
    Vastagh I, Gál A, Reményi V, Semjén J, Lukács T, Valikovics A, Molnár MJ.
    Ideggyogy Sz; 2011 Nov 30; 64(11-12):399-403. PubMed ID: 22611618
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  • 15. 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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  • 16. 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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  • 19. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.
    Lahiri D, Sawale VM, Banerjee S, Dubey S, Roy BK, Das SK.
    J Med Case Rep; 2019 Mar 06; 13(1):63. PubMed ID: 30837005
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