These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
67 related articles for article (PubMed ID: 19744395)
21. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation. Mongini T; Doriguzzi C; Chiadò-Piat L; Silvestri G; Servidei S; Palmucci L Clin Neuropathol; 2002; 21(2):72-6. PubMed ID: 12005255 [TBL] [Abstract][Full Text] [Related]
22. [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]
23. 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]
24. 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]
25. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology. Du W; Li W; Chen G; Cao H; Tang H; Tang X; Jin Q; Sun Z; Zhao H; Zhou W; He S; Lv Y; Zhao J; Zhang X Biosens Bioelectron; 2009 Apr; 24(8):2371-6. PubMed ID: 19155171 [TBL] [Abstract][Full Text] [Related]
26. Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation. Smith ML; Hua XY; Marsden DL; Liu D; Kennaway NG; Ngo KY; Haas RH J Clin Endocrinol Metab; 1997 Sep; 82(9):2826-31. PubMed ID: 9284704 [TBL] [Abstract][Full Text] [Related]
27. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection. Marotta R; Reardon K; McKelvie PA; Chiotis M; Chin J; Cook M; Collins SJ J Clin Neurosci; 2009 Sep; 16(9):1223-5. PubMed ID: 19502062 [TBL] [Abstract][Full Text] [Related]
28. A study of familial MELAS: evaluation of A3243G mutation, clinical phenotype, and magnetic resonance spectroscopy-monitored progression. Chen C; Xiong N; Wang Y; Xiong J; Huang J; Zhang Z; Wang T Neurol India; 2012; 60(1):86-9. PubMed ID: 22406788 [TBL] [Abstract][Full Text] [Related]
29. 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; 65(2B):371-6. PubMed ID: 17664998 [TBL] [Abstract][Full Text] [Related]
30. Population prevalence of the MELAS A3243G mutation. Manwaring N; Jones MM; Wang JJ; Rochtchina E; Howard C; Mitchell P; Sue CM Mitochondrion; 2007 May; 7(3):230-3. PubMed ID: 17300999 [TBL] [Abstract][Full Text] [Related]
31. Skeletal muscle gene expression profiling in mitochondrial disorders. Crimi M; Bordoni A; Menozzi G; Riva L; Fortunato F; Galbiati S; Del Bo R; Pozzoli U; Bresolin N; Comi GP FASEB J; 2005 May; 19(7):866-8. PubMed ID: 15728662 [TBL] [Abstract][Full Text] [Related]
32. 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 [TBL] [Abstract][Full Text] [Related]
33. Mitochondrial maculopathy: geographic atrophy of the macula in the MELAS associated A to G 3243 mitochondrial DNA point mutation. Latkany P; Ciulla TA; Cacchillo PF; Malkoff MD Am J Ophthalmol; 1999 Jul; 128(1):112-4. PubMed ID: 10482110 [TBL] [Abstract][Full Text] [Related]
34. Adult-onset of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presenting as acute meningoencephalitis: a case report. Hsu YC; Yang FC; Perng CL; Tso AC; Wong LJ; Hsu CH J Emerg Med; 2012 Sep; 43(3):e163-6. PubMed ID: 20036095 [TBL] [Abstract][Full Text] [Related]
35. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families. Cevoli S; Pallotti F; La Morgia C; Valentino ML; Pierangeli G; Cortelli P; Baruzzi A; Montagna P; Carelli V Cephalalgia; 2010 Aug; 30(8):919-27. PubMed ID: 20656703 [TBL] [Abstract][Full Text] [Related]
36. 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 [TBL] [Abstract][Full Text] [Related]
37. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]. Stratilová L; Zeman J; Hansíková H; Houstĕk J; Hermanská J; Dudková Z; Konrádová V; Hůlková H; Elleder M Cas Lek Cesk; 1998 Jul; 137(14):430-3. PubMed ID: 9748738 [TBL] [Abstract][Full Text] [Related]
38. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes. Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441 [TBL] [Abstract][Full Text] [Related]
39. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis]. de Toledo M; Díaz-Guzmán J; Pérez-Martínez DA; Sáiz-Díaz RA; Rodríguez-Vallejo A; Campos Y Rev Neurol; 2001 Jul 16-31; 33(2):148-50. PubMed ID: 11562875 [TBL] [Abstract][Full Text] [Related]
40. 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 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]