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Items: 1 to 20 of 96

1.

Mitochondrial disease.

Schapira AH.

Lancet. 2006 Jul 1;368(9529):70-82. Review.

PMID:
16815381
2.

Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia.

Calabrese V, Lodi R, Tonon C, D'Agata V, Sapienza M, Scapagnini G, Mangiameli A, Pennisi G, Stella AM, Butterfield DA.

J Neurol Sci. 2005 Jun 15;233(1-2):145-62. Review.

PMID:
15896810
3.

Mitochondrial disorders.

Zeviani M, Carelli V.

Curr Opin Neurol. 2007 Oct;20(5):564-71. Review.

PMID:
17885446
4.

Defects in mitochondrial DNA replication and human disease.

Copeland WC.

Crit Rev Biochem Mol Biol. 2012 Jan-Feb;47(1):64-74. doi: 10.3109/10409238.2011.632763. Review.

5.

Mitochondria.

Chinnery PF, Schon EA.

J Neurol Neurosurg Psychiatry. 2003 Sep;74(9):1188-99. Review.

6.

[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].

Hattori N.

Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):241-62. Review. Japanese.

PMID:
15287506
7.

Mitochondrial diseases of the brain.

Chaturvedi RK, Flint Beal M.

Free Radic Biol Med. 2013 Oct;63:1-29. doi: 10.1016/j.freeradbiomed.2013.03.018. Epub 2013 Apr 6. Review.

PMID:
23567191
8.

Mitochondrial dysfunction in neurodegenerative disorders.

Schapira AH.

Biochim Biophys Acta. 1998 Aug 10;1366(1-2):225-33.

PMID:
9714816
9.

[Mitochondrial disease and mitochondrial DNA depletion syndromes].

Huang CC, Hsu CH.

Acta Neurol Taiwan. 2009 Dec;18(4):287-95. Review. Chinese.

PMID:
20329599
10.

Modeling pathogenic mutations of human twinkle in Drosophila suggests an apoptosis role in response to mitochondrial defects.

Sanchez-Martinez A, Calleja M, Peralta S, Matsushima Y, Hernandez-Sierra R, Whitworth AJ, Kaguni LS, Garesse R.

PLoS One. 2012;7(8):e43954. doi: 10.1371/journal.pone.0043954. Epub 2012 Aug 28.

11.

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

Luoma P, Melberg A, Rinne JO, Kaukonen JA, Nupponen NN, Chalmers RM, Oldfors A, Rautakorpi I, Peltonen L, Majamaa K, Somer H, Suomalainen A.

Lancet. 2004 Sep 4-10;364(9437):875-82.

PMID:
15351195
12.

Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.

Hakonen AH, Goffart S, Marjavaara S, Paetau A, Cooper H, Mattila K, Lampinen M, Sajantila A, Lönnqvist T, Spelbrink JN, Suomalainen A.

Hum Mol Genet. 2008 Dec 1;17(23):3822-35. doi: 10.1093/hmg/ddn280. Epub 2008 Sep 5.

13.

Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders.

Palin EJ, Paetau A, Suomalainen A.

Brain. 2013 Aug;136(Pt 8):2379-92. doi: 10.1093/brain/awt160. Epub 2013 Jun 27.

14.

Mitochondrial myopathies and encephalomyopathies.

Schapira AH, Cock HR.

Eur J Clin Invest. 1999 Oct;29(10):886-98. Review.

PMID:
10583431
15.

Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.

Elpeleg O, Mandel H, Saada A.

J Mol Med (Berl). 2002 Jul;80(7):389-96. Epub 2002 May 24.

PMID:
12110944
16.

Mitochondrial DNA polymerase-gamma and human disease.

Hudson G, Chinnery PF.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R244-52. Review.

17.

The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.

Cohen BH, Naviaux RK.

Methods. 2010 Aug;51(4):364-73. doi: 10.1016/j.ymeth.2010.05.008. Epub 2010 Jun 15. Review.

PMID:
20558295
18.

Mitochondrial medicine for aging and neurodegenerative diseases.

Reddy PH.

Neuromolecular Med. 2008;10(4):291-315. doi: 10.1007/s12017-008-8044-z. Epub 2008 Jun 20. Review.

19.

Coenzyme Q10 in neuromuscular and neurodegenerative disorders.

Mancuso M, Orsucci D, Volpi L, Calsolaro V, Siciliano G.

Curr Drug Targets. 2010 Jan;11(1):111-21. Review.

PMID:
20017723
20.

Inherited mitochondrial diseases of DNA replication.

Copeland WC.

Annu Rev Med. 2008;59:131-46. Review.

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