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3. Epilepsy Characteristics and Clinical Outcome in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS). Lee HN; Eom S; Kim SH; Kang HC; Lee JS; Kim HD; Lee YM Pediatr Neurol; 2016 Nov; 64():59-65. PubMed ID: 27671241 [TBL] [Abstract][Full Text] [Related]
4. Focal and Generalized Seizures May Occur in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes (MELAS) Patients. Finsterer J; Zarrouk-Mahjoub S J Child Neurol; 2015 Oct; 30(11):1553-4. PubMed ID: 25637648 [No Abstract] [Full Text] [Related]
5. MELAS with A3243G mutation presenting with occipital status epilepticus. Karkare S; Merchant S; Solomon G; Engel M; Kosofsky B J Child Neurol; 2009 Dec; 24(12):1564-7. PubMed ID: 19406752 [TBL] [Abstract][Full Text] [Related]
6. Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA. Lin CM; Thajeb P Metab Brain Dis; 2007 Mar; 22(1):105-9. PubMed ID: 17226098 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report. Hoptasz M; Szczuciński A; Losy J Neurol Neurochir Pol; 2014; 48(2):150-3. PubMed ID: 24821643 [TBL] [Abstract][Full Text] [Related]
9. 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; 34(3):235-8. PubMed ID: 16504796 [TBL] [Abstract][Full Text] [Related]
10. Nerve conduction abnormalities in patients with MELAS and the A3243G mutation. Kaufmann P; Pascual JM; Anziska Y; Gooch CL; Engelstad K; Jhung S; DiMauro S; De Vivo DC Arch Neurol; 2006 May; 63(5):746-8. PubMed ID: 16682545 [TBL] [Abstract][Full Text] [Related]
11. 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 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts. Hirano M; Pavlakis SG J Child Neurol; 1994 Jan; 9(1):4-13. PubMed ID: 8151079 [TBL] [Abstract][Full Text] [Related]
13. The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct. Majamaa K; Turkka J; Kärppä M; Winqvist S; Hassinen IE Neurology; 1997 Nov; 49(5):1331-4. PubMed ID: 9371917 [TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA. Tay SK; Shanske S; Crowe C; Shanske A; Schafer I; Pancrudo J; Lu J; Bonilla E; DiMauro S J Child Neurol; 2005 Feb; 20(2):142-6. PubMed ID: 15794182 [TBL] [Abstract][Full Text] [Related]
15. [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; 145(35):1805-9. PubMed ID: 15493224 [TBL] [Abstract][Full Text] [Related]
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17. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498 [TBL] [Abstract][Full Text] [Related]
18. Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Majamaa K; Moilanen JS; Uimonen S; Remes AM; Salmela PI; Kärppä M; Majamaa-Voltti KA; Rusanen H; Sorri M; Peuhkurinen KJ; Hassinen IE Am J Hum Genet; 1998 Aug; 63(2):447-54. PubMed ID: 9683591 [TBL] [Abstract][Full Text] [Related]
19. 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; 402(2):443-7. PubMed ID: 20965148 [TBL] [Abstract][Full Text] [Related]