Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 250

1.

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
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.

4.

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

Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE.

Ann Neurol. 1994 Jul;36(1):109-12.

PMID:
8024249
5.

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.

Vilkki J, Savontaus ML, Kalimo H, Nikoskelainen EK.

Hum Genet. 1989 Jun;82(3):208-12.

PMID:
2567271
6.

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

De Vries DD, Went LN, Bruyn GW, Scholte HR, Hofstra RM, Bolhuis PA, van Oost BA.

Am J Hum Genet. 1996 Apr;58(4):703-11.

7.

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK.

Science. 1988 Dec 9;242(4884):1427-30.

PMID:
3201231
8.

The mitochondrial DNA mutation at position 11778 in Chinese families with Leber's hereditary optic neuropathy.

Zhang L, Huang Y, Li F, Wang S, Zhu B, Zhang Z, Tong Y, Gao J.

Yan Ke Xue Bao. 1994 Sep;10(3):151-6.

PMID:
7744206
9.

Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.

Mashima Y, Saga M, Hiida Y, Oguchi Y, Wakakura M, Kudoh J, Shimizu N.

Invest Ophthalmol Vis Sci. 1995 Jul;36(8):1714-20.

PMID:
7601652
10.

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.

Singh G, Lott MT, Wallace DC.

N Engl J Med. 1989 May 18;320(20):1300-5.

PMID:
2566116
11.

[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
12.

Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.

Black GC, Craig IW, Oostra RJ, Norby S, Rosenberg T, Morten K, Laborde A, Poulton J.

Eye (Lond). 1995;9 ( Pt 4):513-6.

PMID:
7498577
13.

Mitochondrial DNA analysis in Leber's hereditary optic neuropathy.

Barboni P, Mantovani V, Montagna P, Bragliani M, Cortelli P, Lugaresi E, Puddu P, Caramazza R.

Ophthalmic Paediatr Genet. 1992 Dec;13(4):219-26.

PMID:
1488222
14.

[Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China].

Zhang LS, Huang Y, Li FY.

Zhonghua Yi Xue Za Zhi. 1994 Jun;74(6):349-51, 390. Chinese.

PMID:
7994643
15.
16.

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
17.

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.

Johns DR, Berman J.

Biochem Biophys Res Commun. 1991 Feb 14;174(3):1324-30.

PMID:
1900003
18.
19.

Molecular genetics of Leber's hereditary optic neuropathy: study of a six-generation family from Western Australia.

Sudoyo H, Marzuki S, Mastaglia F, Carroll W.

J Neurol Sci. 1992 Mar;108(1):7-17.

PMID:
1352537
20.

Sequence of mitochondrial DNA in patients with multiple sclerosis.

Chalmers RM, Robertson N, DAS Compston, Harding AE.

Ann Neurol. 1996 Aug;40(2):239-43.

PMID:
8773606
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk