132 related articles for article (PubMed ID: 12397426)
1. Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.
Latvala T; Mustonen E; Uusitalo R; Majamaa K
Graefes Arch Clin Exp Ophthalmol; 2002 Oct; 240(10):795-801. PubMed ID: 12397426
[TBL] [Abstract][Full Text] [Related]
2. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
Kärppä M; Herva R; Moslemi AR; Oldfors A; Kakko S; Majamaa K
Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.
Uusimaa J; Moilanen JS; Vainionpää L; Tapanainen P; Lindholm P; Nuutinen M; Löppönen T; Mäki-Torkko E; Rantala H; Majamaa K
Ann Neurol; 2007 Sep; 62(3):278-87. PubMed ID: 17823937
[TBL] [Abstract][Full Text] [Related]
5. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
Kärppä M; Mahjneh I; Karttunen A; Tolonen U; Majamaa K
J Neurol; 2004 May; 251(5):556-63. PubMed ID: 15164188
[TBL] [Abstract][Full Text] [Related]
6. Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNA.
Kärppä M; Syrjälä P; Tolonen U; Majamaa K
J Neurol; 2003 Feb; 250(2):216-21. PubMed ID: 12574954
[TBL] [Abstract][Full Text] [Related]
7. Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.
Moilanen JS; Majamaa K
Eur J Hum Genet; 2001 Jan; 9(1):59-62. PubMed ID: 11175302
[TBL] [Abstract][Full Text] [Related]
8. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
Janssen AJ; Schuelke M; Smeitink JA; Trijbels FJ; Sengers RC; Lucke B; Wintjes LT; Morava E; van Engelen BG; Smits BW; Hol FA; Siers MH; Ter Laak H; van der Knaap MS; Van Spronsen FJ; Rodenburg RJ; van den Heuvel LP
Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Cardiac involvement in adults with m.3243A>G MELAS gene mutation.
Vydt TC; de Coo RF; Soliman OI; Ten Cate FJ; van Geuns RJ; Vletter WB; Schoonderwoerd K; van den Bosch BJ; Smeets HJ; Geleijnse ML
Am J Cardiol; 2007 Jan; 99(2):264-9. PubMed ID: 17223431
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
Munakata K; Iwamoto K; Bundo M; Kato T
Biol Psychiatry; 2005 Mar; 57(5):525-32. PubMed ID: 15737668
[TBL] [Abstract][Full Text] [Related]
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]
13. 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]
14. Mitochondrial DNA (mtDNA) A 3243G mutation associated with an annular perimacular retinal atrophy.
Adjadj E; Mansouri K; Borruat FX
Klin Monbl Augenheilkd; 2008 May; 225(5):462-4. PubMed ID: 18454399
[TBL] [Abstract][Full Text] [Related]
15. Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation.
Jeppesen TD; Schwartz M; Frederiksen AL; Wibrand F; Olsen DB; Vissing J
Arch Neurol; 2006 Dec; 63(12):1701-6. PubMed ID: 17172609
[TBL] [Abstract][Full Text] [Related]
16. Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.
Michaelides M; Jenkins SA; Brantley MA; Andrews RM; Waseem N; Luong V; Gregory-Evans K; Bhattacharya SS; Fitzke FW; Webster AR
Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3085-97. PubMed ID: 16799055
[TBL] [Abstract][Full Text] [Related]
17. Wolff-Parkinson-White syndrome in Patients With MELAS.
Sproule DM; Kaufmann P; Engelstad K; Starc TJ; Hordof AJ; De Vivo DC
Arch Neurol; 2007 Nov; 64(11):1625-7. PubMed ID: 17998445
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
Niedermayr K; Pölzl G; Scholl-Bürgi S; Fauth C; Schweigmann U; Haberlandt E; Albrecht U; Zlamy M; Sperl W; Mayr JA; Karall D
Congenit Heart Dis; 2018 Sep; 13(5):671-677. PubMed ID: 30133155
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]