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Similar articles for PubMed (Select 21763451)

1.

OXPHOS toxicogenomics and Parkinson's disease.

López-Gallardo E, Iceta R, Iglesias E, Montoya J, Ruiz-Pesini E.

Mutat Res. 2011 Nov-Dec;728(3):98-106. doi: 10.1016/j.mrrev.2011.06.004. Epub 2011 Jul 8. Review.

PMID:
21763451
2.

[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
3.

Mitochondrial oxidative phosphorylation defects in Parkinson's disease.

Shoffner JM, Watts RL, Juncos JL, Torroni A, Wallace DC.

Ann Neurol. 1991 Sep;30(3):332-9.

PMID:
1952821
4.

Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.

Autere J, Moilanen JS, Finnilä S, Soininen H, Mannermaa A, Hartikainen P, Hallikainen M, Majamaa K.

Hum Genet. 2004 Jun;115(1):29-35. Epub 2004 Apr 24.

PMID:
15108120
5.

Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.

Fosslien E.

Ann Clin Lab Sci. 2001 Jan;31(1):25-67. Review.

PMID:
11314862
6.

Mitochondria in the etiology and pathogenesis of Parkinson's disease.

Schapira AH, Gu M, Taanman JW, Tabrizi SJ, Seaton T, Cleeter M, Cooper JM.

Ann Neurol. 1998 Sep;44(3 Suppl 1):S89-98. Review.

PMID:
9749579
7.

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

Gómez-Durán A, Pacheu-Grau D, López-Gallardo E, Díez-Sánchez C, Montoya J, López-Pérez MJ, Ruiz-Pesini E.

Hum Mol Genet. 2010 Sep 1;19(17):3343-53. doi: 10.1093/hmg/ddq246. Epub 2010 Jun 21.

8.

Mitochondrial disorders due to nuclear OXPHOS gene defects.

Ugalde C, Morán M, Blázquez A, Arenas J, Martín MA.

Adv Exp Med Biol. 2009;652:85-116. doi: 10.1007/978-90-481-2813-6_7. Review.

PMID:
20225021
9.

Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patients.

DiDonato S, Zeviani M, Giovannini P, Savarese N, Rimoldi M, Mariotti C, Girotti F, Caraceni T.

Neurology. 1993 Nov;43(11):2262-8.

PMID:
8232940
10.

Mitochondrial dysfunction in neurodegenerative disorders.

Schapira AH.

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

PMID:
9714816
11.

Histochemical methods for the diagnosis of mitochondrial diseases.

De Paepe B, De Bleecker JL, Van Coster R.

Curr Protoc Hum Genet. 2009 Oct;Chapter 19:Unit19.2. doi: 10.1002/0471142905.hg1902s63.

PMID:
19806589
12.

Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease.

Simon DK, Mayeux R, Marder K, Kowall NW, Beal MF, Johns DR.

Neurology. 2000 Feb 8;54(3):703-9.

PMID:
10680807
13.

Environment, mitochondria, and Parkinson's disease.

Sherer TB, Betarbet R, Greenamyre JT.

Neuroscientist. 2002 Jun;8(3):192-7. Review.

PMID:
12061498
14.

Mitochondrial-nuclear co-evolution and its effects on OXPHOS activity and regulation.

Bar-Yaacov D, Blumberg A, Mishmar D.

Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):1107-11. doi: 10.1016/j.bbagrm.2011.10.008. Epub 2011 Oct 22. Review.

PMID:
22044624
15.

Age-environment and gene-environment interactions in the pathogenesis of Parkinson's disease.

Le Couteur DG, Muller M, Yang MC, Mellick GD, McLean AJ.

Rev Environ Health. 2002 Jan-Mar;17(1):51-64. Review.

PMID:
12088093
16.

A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.

Khusnutdinova E, Gilyazova I, Ruiz-Pesini E, Derbeneva O, Khusainova R, Khidiyatova I, Magzhanov R, Wallace DC.

Ann N Y Acad Sci. 2008 Dec;1147:1-20. doi: 10.1196/annals.1427.001.

PMID:
19076426
17.

Oxidative phosphorylation disease diagnosis.

Shoffner JM.

Semin Neurol. 1999;19(4):341-51. Review.

PMID:
10716657
18.

Mitochondrial myopathies and encephalomyopathies.

Schapira AH, Cock HR.

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

PMID:
10583431
19.

A mitochondrial paradigm for degenerative diseases and ageing.

Wallace DC.

Novartis Found Symp. 2001;235:247-63; discussion 263-6. Review.

PMID:
11280029
20.

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

Huerta C, Castro MG, Coto E, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, Martínez C, Lahoz CH, Alvarez V.

J Neurol Sci. 2005 Sep 15;236(1-2):49-54.

PMID:
15975594
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