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Items: 1 to 20 of 340

1.

The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction.

Eichhorn-Mulligan K, Cestari DM.

Semin Ophthalmol. 2008 Jan-Feb;23(1):27-37. doi: 10.1080/08820530701745207. Review.

PMID:
18214789
2.

White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.

Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.

Eur J Paediatr Neurol. 2002;6(2):121-3.

PMID:
11995959
3.

Leber hereditary optic neuropathy: clinical and molecular genetic findings.

Huoponen K.

Neurogenetics. 2001 Jul;3(3):119-25. Review.

PMID:
11523562
4.

Clinical variability in maternally inherited leber hereditary optic neuropathy with the G14459A mutation.

Tarnopolsky MA, Baker SK, Myint T, Maxner CE, Robitaille J, Robinson BH.

Am J Med Genet A. 2004 Feb 1;124A(4):372-6.

PMID:
14735584
5.

[Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].

Chelstowska J, Mroczek K, Niebudek D, Małecka-Idzikowska A, Bartnik E, Hanna Nizankowska M, Sasiadek M.

Przegl Lek. 2002;59(10):777-9. Polish.

PMID:
12632910
6.

Leber hereditary optic neuropathy associated with use of ephedra alkaloids.

Warner RB, Lee AG.

Am J Ophthalmol. 2002 Dec;134(6):918-20.

PMID:
12470769
7.

Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.

Rasool N, Lessell S, Cestari DM.

Semin Ophthalmol. 2016;31(1-2):107-16. doi: 10.3109/08820538.2015.1115251. Review.

PMID:
26959136
8.

[A method for estimating penetrance of pathogenic mutations in a mitochondrial genome].

Kirichenko AV, Zhadanov SI, Aksenovich TI.

Genetika. 2002 Jul;38(7):992-4. Russian.

PMID:
12174593
9.

[Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].

Rydzanicz M, Mrugacz M, Gajecka M.

Klin Oczna. 2008;110(7-9):321-4. Review. Polish.

PMID:
19112871
10.
11.

LHON and other optic nerve atrophies: the mitochondrial connection.

Howell N.

Dev Ophthalmol. 2003;37:94-108. Review.

PMID:
12876832
12.

Leber hereditary optic neuropathy - historical report in comparison with the current knowledge.

Piotrowska A, Korwin M, Bartnik E, Tońska K.

Gene. 2015 Jan 15;555(1):41-9. doi: 10.1016/j.gene.2014.09.048. Epub 2014 Sep 26.

PMID:
25261848
13.

Reduced frequency of known mutations in a cohort of LHON patients from India.

Sundaresan P, Kumar SM, Thompson S, Fingert JH.

Ophthalmic Genet. 2010 Dec;31(4):196-9. doi: 10.3109/13816810.2010.510818. Epub 2010 Sep 1.

PMID:
20809775
14.

Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.

Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Luangtrakool K, Kunhapan B, Lertrit P.

J Hum Genet. 2006;51(12):1110-7. Epub 2006 Oct 28.

PMID:
17072496
15.

[The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].

Mao YJ, Qu J, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):45-9. Review. Chinese.

PMID:
18247303
16.

[Leber's hereditary optic neuropathy].

Hilo W, Jabaly-Habib H, Modi N, Briscoe D.

Harefuah. 2013 Aug;152(8):486-9, 498, 497. Review. Hebrew.

PMID:
24167936
17.

Mitochondrial abnormalities in patients with LHON-like optic neuropathies.

Abu-Amero KK, Bosley TM.

Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4211-20.

PMID:
17003408
18.

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.

Jia X, Li S, Xiao X, Guo X, Zhang Q.

J Hum Genet. 2006;51(10):851-6. Epub 2006 Sep 14.

PMID:
16972023
19.

[Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].

Zheng ML, Zhang GL, Hua AL, Zhang YL.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):166-7. Chinese.

PMID:
15079802
20.

Leber's hereditary optic neuropathy: a multifactorial disease.

Yen MY, Wang AG, Wei YH.

Prog Retin Eye Res. 2006 Jul;25(4):381-96. Epub 2006 Jul 7. Review.

PMID:
16829155

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