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Items: 1 to 20 of 163

1.

Mitochondrial DNA variation in human evolution and disease.

Wallace DC, Brown MD, Lott MT.

Gene. 1999 Sep 30;238(1):211-30. Review.

PMID:
10570998
2.

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.

Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N.

Brain. 2001 Jan;124(Pt 1):209-18.

3.

Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.

Yen MY, Lee HC, Wang AG, Chang WL, Liu JH, Wei YH.

Jpn J Ophthalmol. 1999 May-Jun;43(3):196-200.

PMID:
10413253
4.

Mitochondrial DNA mutations in diseases of energy metabolism.

Wallace DC.

J Bioenerg Biomembr. 1994 Jun;26(3):241-50. Review.

PMID:
8077179
5.

Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy.

Chalmers RM, Schapira AH.

Biochim Biophys Acta. 1999 Feb 9;1410(2):147-58. Review.

6.

Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis.

Mojon DS, Fujihara K, Hirano M, Miller C, Lincoff NS, Jacobs LD, Greenberg SJ.

Graefes Arch Clin Exp Ophthalmol. 1999 Apr;237(4):348-50.

PMID:
10208269
7.

Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.

Carelli V, Ghelli A, Ratta M, Bacchilega E, Sangiorgi S, Mancini R, Leuzzi V, Cortelli P, Montagna P, Lugaresi E, Degli Esposti M.

Neurology. 1997 Jun;48(6):1623-32.

PMID:
9191778
8.

[Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].

Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.

Rev Neurol (Paris). 2001 May;157(5):537-41. French.

PMID:
11438773
9.

[Leber's hereditary optic neuropathy].

Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.

Cas Lek Cesk. 1999 Oct 20;138(18):565-8. Czech.

PMID:
10596473
10.

Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.

Brown MD, Zhadanov S, Allen JC, Hosseini S, Newman NJ, Atamonov VV, Mikhailovskaya IE, Sukernik RI, Wallace DC.

Hum Genet. 2001 Jul;109(1):33-9.

PMID:
11479733
12.

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

Vanopdenbosch L, Dubois B, D'Hooghe MB, Meire F, Carton H.

J Neurol. 2000 Jul;247(7):535-43.

PMID:
10993496
13.
14.

Mitochondrial DNA mutations in human degenerative diseases and aging.

Wallace DC, Shoffner JM, Trounce I, Brown MD, Ballinger SW, Corral-Debrinski M, Horton T, Jun AS, Lott MT.

Biochim Biophys Acta. 1995 May 24;1271(1):141-51. Review.

PMID:
7599200
15.

[Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy].

Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):397-400. Chinese.

PMID:
17680528
16.

Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.

Sudoyo H, Sitepu M, Malik S, Poesponegoro HD, Marzuki S.

Hum Mutat. 1998;Suppl 1:S271-4. No abstract available.

PMID:
9452107
17.

Mitochondrial DNA and human evolution.

Stoneking M.

J Bioenerg Biomembr. 1994 Jun;26(3):251-9. Review.

PMID:
8077180
18.

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC.

Hum Genet. 2002 Feb;110(2):130-8. Epub 2002 Jan 24.

PMID:
11935318
19.

[A case of Leber optic neuropathy with a new point mutation in the cytochrome b gene].

Besch D, Wissinger B, Zrenner E, Leo-Kotter B.

Ophthalmologe. 2000 Jan;97(1):22-6. German.

PMID:
10663786
20.

A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.

Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.

J Neuroophthalmol. 1998 Jun;18(2):81-3.

PMID:
9621260
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