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6. Mitochondrial DNA in stroke and migraine with aura. Ojaimi J; Katsabanis S; Bower S; Quigley A; Byrne E Cerebrovasc Dis; 1998; 8(2):102-6. PubMed ID: 9548008 [TBL] [Abstract][Full Text] [Related]
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10. Hereditary and acquired risk factors for childhood stroke. Riikonen R; Santavuori P Neuropediatrics; 1994 Oct; 25(5):227-33. PubMed ID: 7885530 [TBL] [Abstract][Full Text] [Related]
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12. 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; 9(2):115-22. PubMed ID: 19460299 [TBL] [Abstract][Full Text] [Related]
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15. [Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation]. Ma YN; Fang F; Cao YY; Yang YL; Zou LP; Zhang Y; Wang ST; Zhu SN; Li L; Zheng XF; Pei P; Wu HR; Xiao Y; Qi Y Zhonghua Yi Xue Za Zhi; 2010 Dec; 90(45):3184-7. PubMed ID: 21223764 [TBL] [Abstract][Full Text] [Related]
16. Follow-up in carriers of the 'MELAS' mutation without strokes. Damian MS; Hertel A; Seibel P; Reichmann H; Bachmann G; Schachenmayr W; Hoer G; Dorndorf W Eur Neurol; 1998; 39(1):9-15. PubMed ID: 9476718 [TBL] [Abstract][Full Text] [Related]
17. 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 [TBL] [Abstract][Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Guo Y; Guo Z; Chen L; Zhang J; Wang W; Liu X; Ren H; Gao S Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417 [TBL] [Abstract][Full Text] [Related]
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