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Results: 1 to 20 of 103

1.

Mitochondrial A3243G mutation with manifestation of acute dilated cardiomyopathy.

Stalder N, Yarol N, Tozzi P, Rotman S, Morris M, Fellmann F, Schwitter J, Hullin R.

Circ Heart Fail. 2012 Jan;5(1):e1-3. doi: 10.1161/CIRCHEARTFAILURE.111.963900. No abstract available.

PMID:
22253408
[PubMed - indexed for MEDLINE]
Free Article
2.

Up to date in pharmacological treatment of dilated cardiomyopathy.

Ginghina C, Teodorescu A, Stoian I, Serban M, Ghiorghiu I, Wohlfart K.

Rom J Intern Med. 2004;42(1):3-13. Review.

PMID:
15529591
[PubMed - indexed for MEDLINE]
3.

[Mitochondrial cardiomyopathy].

Tanaka M.

Nihon Rinsho. 2002 Apr;60 Suppl 4:306-11. Review. Japanese. No abstract available.

PMID:
12013873
[PubMed - indexed for MEDLINE]
4.

Cardiomyopathy. Diagnosis and management of dilated cardiomyopathy.

Elliott P.

Heart. 2000 Jul;84(1):106-12. Review. No abstract available.

PMID:
10862601
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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]
6.

Are Angiotensin-converting enzyme inhibitors and beta-blockers ineffective in children with dilated cardiomyopathy and heart failure?

Singh TP, Almond C.

J Am Coll Cardiol. 2010 Aug 31;56(10):823; author reply 823-4. doi: 10.1016/j.jacc.2010.04.037. No abstract available.

PMID:
20797500
[PubMed - indexed for MEDLINE]
Free Article
7.

Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA.

Lin CM, Thajeb P.

Metab Brain Dis. 2007 Mar;22(1):105-9. Epub 2007 Jan 17. Erratum in: Metab Brain Dis. 2007 Dec;22(3-4):425.

PMID:
17226098
[PubMed - indexed for MEDLINE]
8.

Effect of the addition of a beta-blocker on left ventricular remodeling and prognosis in patients with dilated cardiomyopathy treated with angiotensin-converting enzyme inhibitor.

Hamada M, Hara Y, Ohtsuka T, Suzuki J, Saeki H, Ogimoto A, Shigematsu Y.

J Cardiovasc Pharmacol. 2003 Jan;41 Suppl 1:S5-10.

PMID:
12688389
[PubMed - indexed for MEDLINE]
9.

[Peculiarities of cardiac failure treatment in diffuse myocarditis and dilated cardiomyopathy].

Gurevich MA, Iankovskaia MO, Gordienko BV, Mravian SR, Grigor'eva NM.

Klin Med (Mosk). 1997;75(1):48-50. Review. Russian. No abstract available.

PMID:
9082062
[PubMed - indexed for MEDLINE]
10.

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).

De Kremer RD, Paschini-Capra A, Bacman S, Argaraña C, Civallero G, Kelley RI, Guelbert N, Latini A, de Halac IN, Giner-Ayala A, Johnston J, Proujansky R, Gonzalez I, Depetris-Boldini C, Oller-Ramírez A, Angaroni C, Theaux RA, Hliba E, Juaneda E.

Am J Med Genet. 2001 Mar 1;99(2):83-93.

PMID:
11241464
[PubMed - indexed for MEDLINE]
11.

MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions.

Aharoni S, Traves TA, Melamed E, Cohen S, Silver EL.

J Neurol Sci. 2010 Sep 15;296(1-2):101-3. doi: 10.1016/j.jns.2010.06.029. Epub 2010 Jul 22.

PMID:
20655066
[PubMed - indexed for MEDLINE]
12.

[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]
13.

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]
14.

Pathogenesis and treatment of cardiomyopathy.

Fonarow GC.

Adv Intern Med. 2001;47:1-45. Review.

PMID:
11795071
[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.

The mitochondrial A3243G mutation presenting as severe cardiomyopathy.

Vilarinho L, Santorelli FM, Rosas MJ, Tavares C, Melo-Pires M, DiMauro S.

J Med Genet. 1997 Jul;34(7):607-9.

PMID:
9222976
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

A boy with muscle weakness, hypercarbia, and the mitochondrial DNA A3243G mutation.

Saneto RP, Bouldin A.

J Child Neurol. 2006 Jan;21(1):77-9.

PMID:
16551459
[PubMed - indexed for MEDLINE]
19.

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
20.

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 Jan-Feb;60(1):86-9. doi: 10.4103/0028-3886.93609.

PMID:
22406788
[PubMed - indexed for MEDLINE]
Free Article
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