156 related articles for article (PubMed ID: 29376197)
1. Mitochondrial A3243G mutation results in corneal endothelial polymegathism.
Bakhoum MF; Wu WP; White EC; Sengillo JD; Sanfilippo C; Morcos MM; Freund KB; Perry HD; Sarraf D; Tsang SH
Graefes Arch Clin Exp Ophthalmol; 2018 Mar; 256(3):583-588. PubMed ID: 29376197
[TBL] [Abstract][Full Text] [Related]
2. Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members.
Michaelides M; Jenkins SA; Bamiou DE; Sweeney MG; Davis MB; Luxon L; Bird AC; Rath PP
Arch Ophthalmol; 2008 Mar; 126(3):320-8. PubMed ID: 18332310
[TBL] [Abstract][Full Text] [Related]
3. The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients.
Kaisari E; Borruat FX
Klin Monbl Augenheilkd; 2021 Apr; 238(4):414-417. PubMed ID: 33930928
[TBL] [Abstract][Full Text] [Related]
4. 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; 8(10):13411-5. PubMed ID: 26722549
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence.
Rath PP; Jenkins S; Michaelides M; Smith A; Sweeney MG; Davis MB; Fitzke FW; Bird AC
Br J Ophthalmol; 2008 May; 92(5):623-9. PubMed ID: 18441172
[TBL] [Abstract][Full Text] [Related]
7. Clinical features of A3243G mitochondrial tRNA mutation.
Chae JH; Hwang H; Lim BC; Cheong HI; Hwang YS; Kim KJ
Brain Dev; 2004 Oct; 26(7):459-62. PubMed ID: 15351082
[TBL] [Abstract][Full Text] [Related]
8. MELAS A3243G mitochondrial DNA mutation and age related maculopathy.
Jones M; Mitchell P; Wang JJ; Sue C
Am J Ophthalmol; 2004 Dec; 138(6):1051-3. PubMed ID: 15629304
[TBL] [Abstract][Full Text] [Related]
9. Distinctive distribution of brain volume reductions in MELAS and mitochondrial DNA A3243G mutation carriers: A voxel-based morphometric study.
Tsujikawa K; Senda J; Yasui K; Hasegawa Y; Hoshiyama M; Katsuno M; Sobue G
Mitochondrion; 2016 Sep; 30():229-35. PubMed ID: 27558483
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy.
Harrison TJ; Boles RG; Johnson DR; LeBlond C; Wong LJ
Am J Ophthalmol; 1997 Aug; 124(2):217-21. PubMed ID: 9262546
[TBL] [Abstract][Full Text] [Related]
13. Corneal guttata associated with the corneal dystrophy resulting from a betaig-h3 R124H mutation.
Akimune C; Watanabe H; Maeda N; Okada M; Yamamoto S; Kiritoshi A; Inoue Y; Shimomura Y; Tano Y
Br J Ophthalmol; 2000 Jan; 84(1):67-71. PubMed ID: 10611102
[TBL] [Abstract][Full Text] [Related]
14. The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.
Iwasaki S; Egami N; Fujimoto C; Chihara Y; Ushio M; Kashio A; Yamasoba T
Laryngoscope; 2011 Aug; 121(8):1821-4. PubMed ID: 21792976
[TBL] [Abstract][Full Text] [Related]
15. Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: a single-step approach.
Bai RK; Wong LJ
Clin Chem; 2004 Jun; 50(6):996-1001. PubMed ID: 15073091
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Mitochondrial DNA A3243G variant-associated retinopathy: a meta-analysis of the clinical course of visual acuity and correlation with systemic manifestations.
Coussa RG; Sohn EH; Han IC; Parikh S; Traboulsi EI
Ophthalmic Genet; 2021 Aug; 42(4):420-430. PubMed ID: 33827363
[TBL] [Abstract][Full Text] [Related]
18. Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.
Vielhaber S; Varlamov DA; Kudina TA; Schröder R; Kappes-Horn K; Elger CE; Seibel M; Seibel P; Kunz WS
J Neuropathol Exp Neurol; 2002 Oct; 61(10):885-95. PubMed ID: 12387454
[TBL] [Abstract][Full Text] [Related]
19. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
