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Results: 1 to 20 of 95

1.

MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.

Prasad M, Narayan B, Prasad AN, Rupar CA, Levin S, Kronick J, Ramsay D, Tay KY, Prasad C.

Can J Neurol Sci. 2014 Mar;41(2):210-9. No abstract available.

PMID:
24534033
[PubMed - in process]
2.

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.

PMID:
12150728
[PubMed - indexed for MEDLINE]
Free Article
3.

mtDNA A3243G MELAS mutation is not associated with multigenerational female migraine.

Buzzi MG, Di Gennaro G, D'Onofrio M, Ciccarelli O, Santorelli FM, Fortini D, Nappi G, Nicoletti F, Casali C.

Neurology. 2000 Feb 22;54(4):1005-7.

PMID:
10691007
[PubMed - indexed for MEDLINE]
4.

[Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].

Ma YN, Fang F, Yang YL, Zhang Y, Wang ST, Xu YF, Pei P, Yuan Y, Bu DF, Qi Y.

Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3250-3. Chinese.

PMID:
19159547
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
16504796
[PubMed - indexed for MEDLINE]
6.

Bilateral Polymicrogyria and MELAS/A3243G Mutation. A Very Uncommon Association.

Vidal A, Castillo M.

Neuroradiol J. 2011 May 15;24(2):199-201. Epub 2011 May 11.

PMID:
24059608
[PubMed]
7.

Atypical clinical presentations of the A3243G mutation, usually associated with MELAS.

Blum S, Robertson T, Klingberg S, Henderson RD, McCombe P.

Intern Med J. 2011 Feb;41(2):199-202. doi: 10.1111/j.1445-5994.2010.02379.x.

PMID:
22747555
[PubMed - indexed for MEDLINE]
8.

The study of mitochondrial A3243G mutation in different samples.

Ma Y, Fang F, Yang Y, Zou L, Zhang Y, Wang S, Xu Y, Pei P, Qi Y.

Mitochondrion. 2009 Apr;9(2):139-43. doi: 10.1016/j.mito.2009.01.004. Epub 2009 Jan 21.

PMID:
19460298
[PubMed - indexed for MEDLINE]
9.

A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.

Hsieh RH, Li JY, Pang CY, Wei YH.

J Biomed Sci. 2001 Jul-Aug;8(4):328-35.

PMID:
11455195
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
17998445
[PubMed - indexed for MEDLINE]
11.

[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].

Delgado-Sánchez R, Zárate-Moysen A, Monsalvo-Reyes A, Herrero MD, Ruiz-Pesini E, López-Pérez M, Montoya J, Montiel-Sosa JF.

Rev Neurol. 2007 Jan 1-15;44(1):18-22. Spanish.

PMID:
17199225
[PubMed - indexed for MEDLINE]
Free Article
12.

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.

PMID:
16682545
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
15629304
[PubMed - indexed for MEDLINE]
14.

Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.

Mehrazin M, Shanske S, Kaufmann P, Wei Y, Coku J, Engelstad K, Naini A, De Vivo DC, DiMauro S.

Am J Med Genet A. 2009 Feb 15;149A(4):584-7. doi: 10.1002/ajmg.a.32703.

PMID:
19253345
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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.

PMID:
15351082
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
10645055
[PubMed - indexed for MEDLINE]
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.

PMID:
10660156
[PubMed - indexed for MEDLINE]
18.

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 Mar-Apr;21(2):72-6.

PMID:
12005255
[PubMed - indexed for MEDLINE]
19.

A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome.

Li JY, Hsieh RH, Peng NJ, Lai PH, Lee CF, Lo YK, Wei YH.

J Formos Med Assoc. 2007 Jul;106(7):528-36.

PMID:
17660142
[PubMed - indexed for MEDLINE]
20.

A False-Positive Diagnosis for the Common MELAS (A3243G) Mutation Caused by a Novel Variant (A3426G) in the ND1 Gene of Mitochondria DNA.

Kirby DM, Milovac T, Thorburn DR.

Mol Diagn. 1998 Dec;3(4):211-215.

PMID:
10089279
[PubMed - as supplied by publisher]

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