Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 28

1.

The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.

Hammans SR, Sweeney MG, Brockington M, Lennox GG, Lawton NF, Kennedy CR, Morgan-Hughes JA, Harding AE.

Brain. 1993 Jun;116 ( Pt 3):617-32.

PMID:
8513395
[PubMed - indexed for MEDLINE]
2.

Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.

Virgilio R, Ronchi D, Bordoni A, Fassone E, Bonato S, Donadoni C, Torgano G, Moggio M, Corti S, Bresolin N, Comi GP.

J Neurol Sci. 2009 Jun 15;281(1-2):85-92. doi: 10.1016/j.jns.2009.01.025. Epub 2009 Mar 10. Review.

PMID:
19278689
[PubMed - indexed for MEDLINE]
3.

[Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].

Tanno Y, Yoneda M, Tanaka K, Tsuji S.

Nihon Rinsho. 1993 Sep;51(9):2379-85. Review. Japanese.

PMID:
8411716
[PubMed - indexed for MEDLINE]
4.

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas.

Larsson NG, Tulinius MH, Holme E, Oldfors A.

Muscle Nerve Suppl. 1995;3:S102-6. Review.

PMID:
7603509
[PubMed - indexed for MEDLINE]
5.

Mitochondrial diseases.

Nonaka I.

Curr Opin Neurol Neurosurg. 1992 Oct;5(5):622-32. Review.

PMID:
1392136
[PubMed - indexed for MEDLINE]
6.

MERRF: a model disease for understanding the principles of mitochondrial genetics.

Shoffner JM, Lott MT, Wallace DC.

Rev Neurol (Paris). 1991;147(6-7):431-5. Review.

PMID:
1962048
[PubMed - indexed for MEDLINE]
7.

Diseases resulting from mitochondrial DNA point mutations.

Wallace DC, Lott MT, Shoffner JM, Brown MD.

J Inherit Metab Dis. 1992;15(4):472-9. Review.

PMID:
1528007
[PubMed - indexed for MEDLINE]
8.

[MERRF (myoclonus epilepsy associated with ragged-red fibers)].

Goto Y.

Ryoikibetsu Shokogun Shirizu. 2001;(36):150-2. Review. Japanese. No abstract available.

PMID:
11596350
[PubMed - indexed for MEDLINE]
9.

Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.

Wu SB, Ma YS, Wu YT, Chen YC, Wei YH.

Mol Neurobiol. 2010 Jun;41(2-3):256-66. doi: 10.1007/s12035-010-8123-7. Epub 2010 Apr 23. Review.

PMID:
20411357
[PubMed - indexed for MEDLINE]
10.

[Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].

Suzuki S.

Nihon Rinsho. 1994 Oct;52(10):2606-10. Review. Japanese.

PMID:
7527090
[PubMed - indexed for MEDLINE]
11.

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems.

Attardi G, Yoneda M, Chomyn A.

Biochim Biophys Acta. 1995 May 24;1271(1):241-8. Review.

PMID:
7599215
[PubMed - indexed for MEDLINE]
12.

[Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF].

Goto Y.

Nihon Rinsho. 1997 Dec;55(12):3259-64. Review. Japanese.

PMID:
9436447
[PubMed - indexed for MEDLINE]
13.

Mitochondrial DNA mutations in diseases of energy metabolism.

Wallace DC.

J Bioenerg Biomembr. 1994 Jun;26(3):241-50. Review.

PMID:
8077179
[PubMed - indexed for MEDLINE]
14.

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study.

Berkovic SF, Carpenter S, Evans A, Karpati G, Shoubridge EA, Andermann F, Meyer E, Tyler JL, Diksic M, Arnold D, et al.

Brain. 1989 Oct;112 ( Pt 5):1231-60. Review.

PMID:
2508988
[PubMed - indexed for MEDLINE]
15.

Human mitochondrial diseases: answering questions and questioning answers.

Howell N.

Int Rev Cytol. 1999;186:49-116. Review.

PMID:
9770297
[PubMed - indexed for MEDLINE]
16.

[Diseases caused by mitochondrial DNA mutations].

Wijburg FA, van den Bogert C, de Visser M, Oostra RJ, Bakker PA, Bolhuis PA.

Ned Tijdschr Geneeskd. 1995 Jul 1;139(26):1322-6. Review. Dutch. No abstract available.

PMID:
7617049
[PubMed - indexed for MEDLINE]
17.

Mitochondrial DNA alterations and genetic diseases: a review.

Lestienne P, Bataillé N.

Biomed Pharmacother. 1994;48(5-6):199-214. Review.

PMID:
7999980
[PubMed - indexed for MEDLINE]
18.

Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review.

Geny C, Cormier V, Meyrignac C, Cesaro P, Degos JD, Gherardi R, Rötig A.

J Neurol. 1991 Jun;238(3):171-6. Review.

PMID:
1908005
[PubMed - indexed for MEDLINE]
19.

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Mita S, Tokunaga M, Kumamoto T, Uchino M, Nonaka I, Ando M.

Muscle Nerve Suppl. 1995;3:S113-8. Review.

PMID:
7603511
[PubMed - indexed for MEDLINE]
20.

[The correlation of the heteroplasmy of mtDNA and clinicopathological findings in the patients with mitochondrial encephalomyopathies].

Tanno Y, Tanaka K, Tsuji S.

Nihon Rinsho. 1997 Dec;55(12):3270-6. Review. Japanese.

PMID:
9436449
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk