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Results: 1 to 20 of 102

1.

Prognosis of symptomatic patients with the A3243G mutation of mitochondrial DNA.

Liu CH, Chang CH, Kuo HC, Ro LS, Liou CW, Wei YH, Huang CC.

J Formos Med Assoc. 2012 Sep;111(9):489-94. doi: 10.1016/j.jfma.2011.06.014. Epub 2012 Apr 18.

PMID:
23021505
[PubMed - indexed for MEDLINE]
2.

Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.

Huang CC, Kuo HC, Chu CC, Liou CW, Ma YS, Wei YH.

J Biomed Sci. 2002;9(6 Pt 1):527-33.

PMID:
12372990
[PubMed - indexed for MEDLINE]
3.

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]
4.

Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.

Lien LM, Lee HC, Wang KL, Chiu JC, Chiu HC, Wei YH.

Acta Neurol Scand. 2001 Mar;103(3):159-65.

PMID:
11240563
[PubMed - indexed for MEDLINE]
5.

Molecular analysis of diabetes mellitus-associated A3243G mitochondrial DNA mutation in Taiwanese cases.

Liou CW, Huang CC, Wei YH.

Diabetes Res Clin Pract. 2001 Dec;54 Suppl 2:S39-43.

PMID:
11733108
[PubMed - indexed for MEDLINE]
6.

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan.

Lee YC, Lu YC, Chang MH, Soong BW.

J Neurol Sci. 2007 Mar 15;254(1-2):65-8. Epub 2007 Feb 14.

PMID:
17300808
[PubMed - indexed for MEDLINE]
7.

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]
8.

External ophthalmoplegia with severe progressive multiorgan involvement associated with the mtDNA A3243G mutation.

Hansrote S, Croul S, Selak M, Kalman B, Schwartzman RJ.

J Neurol Sci. 2002 May 15;197(1-2):63-7.

PMID:
11997068
[PubMed - indexed for MEDLINE]
9.

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.

PMID:
9371917
[PubMed - indexed for MEDLINE]
10.

Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.

Pang CY, Huang CC, Yen MY, Wang EK, Kao KP, Chen SS, Wei YH.

J Formos Med Assoc. 1999 May;98(5):326-34.

PMID:
10420700
[PubMed - indexed for MEDLINE]
11.

Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA.

Majamaa-Voltti K, Turkka J, Kortelainen ML, Huikuri H, Majamaa K.

J Neurol Neurosurg Psychiatry. 2008 Feb;79(2):209-11. doi: 10.1136/jnnp.2007.122648.

PMID:
18202211
[PubMed - indexed for MEDLINE]
12.

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M.

J Neurol. 1995 May;242(5):304-12.

PMID:
7643139
[PubMed - indexed for MEDLINE]
13.

[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. Chinese.

PMID:
15782498
[PubMed - indexed for MEDLINE]
14.

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]
15.

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]
16.

Low antioxidant content and mutation load in mitochondrial DNA A3243G mutation-related diabetes mellitus.

Liou CW, Huang CC, Lee CF, Lin TK, Wei YH.

J Formos Med Assoc. 2003 Aug;102(8):527-33.

PMID:
14569316
[PubMed - indexed for MEDLINE]
17.

Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.

Morovvati S, Nakagawa M, Sato Y, Hamada K, Higuchi I, Osame M.

Acta Neurol Scand. 2002 Aug;106(2):104-8.

PMID:
12100370
[PubMed - indexed for MEDLINE]
18.

Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies.

Cao Y, Ma Y, Zhang Y, Li Y, Fang F, Wang S, Bu D, Xu Y, Pei P, Li L, Xiao Y, Wu H, Yang Y, Zou L, Qi Y.

Mitochondrion. 2010 Jun;10(4):330-4. doi: 10.1016/j.mito.2010.01.008. Epub 2010 Feb 1.

PMID:
20123042
[PubMed - indexed for MEDLINE]
19.

Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy.

Cesaroni E, Scarpelli M, Zamponi N, Polonara G, Zeviani M.

Pediatr Neurol. 2009 Aug;41(2):131-4. doi: 10.1016/j.pediatrneurol.2009.02.018.

PMID:
19589463
[PubMed - indexed for MEDLINE]
20.

Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.

Uusimaa J, Hinttala R, Rantala H, Päivärinta M, Herva R, Röyttä M, Soini H, Moilanen JS, Remes AM, Hassinen IE, Majamaa K.

Epilepsia. 2008 Jun;49(6):1038-45. doi: 10.1111/j.1528-1167.2008.01544.x. Epub 2008 Feb 20.

PMID:
18294203
[PubMed - indexed for MEDLINE]
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