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Items: 1 to 20 of 45

1.

Mitochondrial disorders as windows into an ancient organelle.

Vafai SB, Mootha VK.

Nature. 2012 Nov 15;491(7424):374-83. doi: 10.1038/nature11707. Review.

PMID:
23151580
2.

Nuclear gene defects in mitochondrial disorders.

Scaglia F.

Methods Mol Biol. 2012;837:17-34. doi: 10.1007/978-1-61779-504-6_2. Review.

PMID:
22215538
3.

Medicinal and genetic approaches to the treatment of mitochondrial disease.

Schon EA, DiMauro S.

Curr Med Chem. 2003 Dec;10(23):2523-33. Review.

PMID:
14529468
4.

The genetics of mitochondrial disease.

Davis RL, Sue CM.

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

PMID:
22266889
5.

Therapy for mitochondrial disorders: little proof, high research activity, some promise.

Suomalainen A.

Semin Fetal Neonatal Med. 2011 Aug;16(4):236-40. doi: 10.1016/j.siny.2011.05.003. Review.

PMID:
21676668
6.

Current concepts of mitochondrial disorders in childhood.

Borchert A, Wolf NI, Wilichowski E.

Semin Pediatr Neurol. 2002 Jun;9(2):151-9. Review.

PMID:
12138999
7.

[Evolution of the concept of mitochondrial disease].

Desnuelle C.

Bull Acad Natl Med. 2003;187(3):537-55; discussion 555-7. Review. French.

PMID:
14556468
8.

Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits.

Geromel V, Darin N, Chrétien D, Bénit P, DeLonlay P, Rötig A, Munnich A, Rustin P.

Mol Genet Metab. 2002 Sep-Oct;77(1-2):21-30. Review.

PMID:
12359126
9.

Drug-induced mitochondrial neuropathy in children: a conceptual framework for critical windows of development.

Wallace KB.

J Child Neurol. 2014 Sep;29(9):1241-8. doi: 10.1177/0883073814538510. Review.

PMID:
25008905
10.

The contribution of mitochondria to common disorders.

Enns GM.

Mol Genet Metab. 2003 Sep-Oct;80(1-2):11-26. Review.

PMID:
14567954
11.

Less than perfect divorces: dysregulated mitochondrial fission and neurodegeneration.

Oettinghaus B, Licci M, Scorrano L, Frank S.

Acta Neuropathol. 2012 Feb;123(2):189-203. doi: 10.1007/s00401-011-0930-z. Review.

PMID:
22179580
12.

Mitochondrial respiratory chain dysfunction caused by coenzyme Q deficiency.

Rustin P, Munnich A, Rötig A.

Methods Enzymol. 2004;382:81-8. Review. No abstract available.

PMID:
15047097
13.

Multisystem manifestations of mitochondrial disorders.

Di Donato S.

J Neurol. 2009 May;256(5):693-710. doi: 10.1007/s00415-009-5028-3. Review.

PMID:
19252802
14.

Mitochondrial deficiency in Cockayne syndrome.

Scheibye-Knudsen M, Croteau DL, Bohr VA.

Mech Ageing Dev. 2013 May-Jun;134(5-6):275-83. doi: 10.1016/j.mad.2013.02.007. Review.

15.

Mitochondrial biology in Alzheimer's disease pathogenesis.

Galindo MF, Ikuta I, Zhu X, Casadesus G, Jordán J.

J Neurochem. 2010 Aug;114(4):933-45. doi: 10.1111/j.1471-4159.2010.06814.x. Review.

16.

[Mitochondria in cell life, death and disease].

Wojtczak L, Zabłocki K.

Postepy Biochem. 2008;54(2):129-41. Review. Polish.

PMID:
18807924
17.

Mitochondrial respiratory dysfunction-elicited oxidative stress and posttranslational protein modification in mitochondrial diseases.

Wu YT, Wu SB, Lee WY, Wei YH.

Ann N Y Acad Sci. 2010 Jul;1201:147-56. doi: 10.1111/j.1749-6632.2010.05631.x. Review.

PMID:
20649551
18.

Searching for nuclear-mitochondrial genes.

Chinnery PF.

Trends Genet. 2003 Feb;19(2):60-2. Review.

PMID:
12547509
19.

Diagnostic challenges of mitochondrial disorders: complexities of two genomes.

Graham BH.

Methods Mol Biol. 2012;837:35-46. doi: 10.1007/978-1-61779-504-6_3. Review.

PMID:
22215539
20.

Mitochondrial mutations: genotype to phenotype.

Schon EA, DiMauro S.

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

PMID:
18074641
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