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Items: 1 to 20 of 74

1.

Mitochondrial diseases.

DiMauro S.

Biochim Biophys Acta. 2004 Jul 23;1658(1-2):80-8. Review.

2.

Mitochondrial DNA mutations and depletion in pediatric medicine.

Spinazzola A.

Semin Fetal Neonatal Med. 2011 Aug;16(4):190-6. doi: 10.1016/j.siny.2011.04.011. Epub 2011 Jun 8. Review.

PMID:
21652274
3.

Mitochondrial encephalomyopathies.

DiMauro S, Moraes CT.

Arch Neurol. 1993 Nov;50(11):1197-208. Review.

PMID:
8215979
4.

Mitochondrial defects in neurodegenerative disease.

Wallace DC.

Ment Retard Dev Disabil Res Rev. 2001;7(3):158-66. Review.

PMID:
11553931
5.

Mitochondrial mutations: genotype to phenotype.

Schon EA, DiMauro S.

Novartis Found Symp. 2007;287:214-25; discussion 226-33. Review.

PMID:
18074641
6.

Mitochondrial DNA-related disorders.

Mancuso M, Filosto M, Choub A, Tentorio M, Broglio L, Padovani A, Siciliano G.

Biosci Rep. 2007 Jun;27(1-3):31-7. Review.

PMID:
17484046
7.

Diagnostic challenges of mitochondrial DNA disorders.

Wong LJ.

Mitochondrion. 2007 Feb-Apr;7(1-2):45-52. Epub 2006 Dec 12. Review.

PMID:
17276740
8.

Mitochondrial DNA medicine.

DiMauro S.

Biosci Rep. 2007 Jun;27(1-3):5-9. Review.

PMID:
17484047
9.

Bioenergetics of mitochondrial diseases associated with mtDNA mutations.

Lenaz G, Baracca A, Carelli V, D'Aurelio M, Sgarbi G, Solaini G.

Biochim Biophys Acta. 2004 Jul 23;1658(1-2):89-94. Review.

10.

The genetics of mitochondrial disease.

Davis RL, Sue CM.

Semin Neurol. 2011 Nov;31(5):519-30. doi: 10.1055/s-0031-1299790. Epub 2012 Jan 21. Review.

PMID:
22266889
11.

Mitochondrial disorders.

Zeviani M, Di Donato S.

Brain. 2004 Oct;127(Pt 10):2153-72. Epub 2004 Sep 9. Review. Erratum in: Brain. 2004 Dec;127(Pt 12):2783.

PMID:
15358637
12.

[Molecular genetics of alterations in the mitochondrial respiratory chain].

Martín MA, Campos Y, de Bustos F, del Hoyo P, Rubio JC, Arenas J.

Rev Neurol. 1998 Apr;26 Suppl 1:S27-35. Review. Spanish.

PMID:
9810588
13.

Pathogenesis and treatment of mitochondrial disorders.

DiMauro S, Hirano M.

Adv Exp Med Biol. 2009;652:139-70. doi: 10.1007/978-90-481-2813-6_10. Review.

PMID:
20225024
14.

Mitochondrial medicine.

Dimauro S.

Biochim Biophys Acta. 2004 Dec 6;1659(2-3):107-14. Review.

15.

Maternal inheritance and the evaluation of oxidative phosphorylation diseases.

Shoffner JM.

Lancet. 1996 Nov 9;348(9037):1283-8. Review.

PMID:
8909383
16.

[Gene expression profiling of classic mitochondrial disorders. Its value in finding therapeutic strategies].

Mende S, Storch A, Reichmann H.

Nervenarzt. 2007 Oct;78(10):1155-9. Review. German.

PMID:
17458528
17.

[Diseases caused by mutations in mitochondrial DNA].

Wojewoda M, Zabłocki K, Szczepanowska J.

Postepy Biochem. 2011;57(2):222-9. Review. Polish.

PMID:
21913424
18.

Mitochondrial encephalomyopathies: an update.

DiMauro S, Hirano M.

Neuromuscul Disord. 2005 Apr;15(4):276-86. Review.

PMID:
15792866
19.
20.

Human mitochondrial diseases: answering questions and questioning answers.

Howell N.

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

PMID:
9770297

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