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Results: 1 to 20 of 171

Similar articles for PubMed (Select 10502593)

1.

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.

Andreu AL, Hanna MG, Reichmann H, Bruno C, Penn AS, Tanji K, Pallotti F, Iwata S, Bonilla E, Lach B, Morgan-Hughes J, DiMauro S.

N Engl J Med. 1999 Sep 30;341(14):1037-44.

2.

A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.

Dumoulin R, Sagnol I, Ferlin T, Bozon D, Stepien G, Mousson B.

Mol Cell Probes. 1996 Oct;10(5):389-91.

PMID:
8910895
3.

Muscle pain, fatigue, and mitochondriopathies.

Griggs RC, Karpati G.

N Engl J Med. 1999 Sep 30;341(14):1077-8. No abstract available.

PMID:
10502600
4.

Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.

Andreu AL, Bruno C, Shanske S, Shtilbans A, Hirano M, Krishna S, Hayward L, Systrom DS, Brown RH Jr, DiMauro S.

Neurology. 1998 Nov;51(5):1444-7.

PMID:
9818877
5.

Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.

Mancuso M, Filosto M, Stevens JC, Patterson M, Shanske S, Krishna S, DiMauro S.

J Neurol Sci. 2003 May 15;209(1-2):61-3.

PMID:
12686403
6.

POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.

Di Fonzo A, Bordoni A, Crimi M, Sara G, Del Bo R, Bresolin N, Comi GP.

Hum Mutat. 2003 Dec;22(6):498-9.

PMID:
14635118
7.

No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations.

Schwartz M, Vissing J.

J Neurol Sci. 2004 Mar 15;218(1-2):99-101.

PMID:
14759640
8.

Exercise intolerance due to cytochrome b mutation.

Massie R, Wong LJ, Milone M.

Muscle Nerve. 2010 Jul;42(1):136-40. doi: 10.1002/mus.21649.

PMID:
20544923
9.

A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria.

Andreu AL, Bruno C, Dunne TC, Tanji K, Shanske S, Sue CM, Krishna S, Hadjigeorgiou GM, Shtilbans A, Bonilla E, DiMauro S.

Ann Neurol. 1999 Jan;45(1):127-30.

PMID:
9894887
10.

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S.

Neurology. 2000 Sep 12;55(5):644-9.

PMID:
10980727
11.

Mutations in mitochondrial DNA as a cause of exercise intolerance.

DiMauro S, Andreu AL.

Ann Med. 2001 Oct;33(7):472-6. Review.

PMID:
11680795
12.

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.

Filosto M, Mancuso M, Vives-Bauza C, Vilà MR, Shanske S, Hirano M, Andreu AL, DiMauro S.

Ann Neurol. 2003 Oct;54(4):524-6.

PMID:
14520667
13.

Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I.

Kollberg G, Moslemi AR, Lindberg C, Holme E, Oldfors A.

J Neuropathol Exp Neurol. 2005 Feb;64(2):123-8.

PMID:
15751226
14.

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.

Jeppesen TD, Schwartz M, Olsen DB, Wibrand F, Krag T, Dunø M, Hauerslev S, Vissing J.

Brain. 2006 Dec;129(Pt 12):3402-12. Epub 2006 Jun 30.

15.

Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene.

Vives-Bauza C, Gamez J, Roig M, Briones P, Cervera C, Solano A, Montoya J, Andreu AL.

Ann Med. 2001 Oct;33(7):493-6.

PMID:
11680798
16.

Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene.

Bruno C, Santorelli FM, Assereto S, Tonoli E, Tessa A, Traverso M, Scapolan S, Bado M, Tedeschi S, Minetti C.

Muscle Nerve. 2003 Oct;28(4):508-11.

PMID:
14506725
17.

The expanding clinical spectrum of mitochondrial diseases.

De Vivo DC.

Brain Dev. 1993 Jan-Feb;15(1):1-22. Review.

PMID:
8338207
18.

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW.

Am J Hum Genet. 1998 Jul;63(1):29-36.

19.

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.

Keightley JA, Anitori R, Burton MD, Quan F, Buist NR, Kennaway NG.

Am J Hum Genet. 2000 Dec;67(6):1400-10. Epub 2000 Oct 20.

20.

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.

Sternberg D, Chatzoglou E, Laforêt P, Fayet G, Jardel C, Blondy P, Fardeau M, Amselem S, Eymard B, Lombès A.

Brain. 2001 May;124(Pt 5):984-94.

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