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Items: 1 to 20 of 70

1.

Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy.

Lu Q, Guo Y, Yi J, Deng X, Yang Z, Yuan X, Deng H.

Optom Vis Sci. 2017 Dec;94(12):1090-1094. doi: 10.1097/OPX.0000000000001147.

PMID:
29116953
2.

Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation.

Mashima Y, Kigasawa K, Shinoda K, Wakakura M, Oguchi Y.

BMC Ophthalmol. 2017 Oct 18;17(1):192. doi: 10.1186/s12886-017-0583-3.

3.

International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy.

Carelli V, Carbonelli M, de Coo IF, Kawasaki A, Klopstock T, Lagrèze WA, La Morgia C, Newman NJ, Orssaud C, Pott JWR, Sadun AA, van Everdingen J, Vignal-Clermont C, Votruba M, Yu-Wai-Man P, Barboni P.

J Neuroophthalmol. 2017 Dec;37(4):371-381. doi: 10.1097/WNO.0000000000000570.

PMID:
28991104
4.

Dominant Optic Atrophy and Leber's Hereditary Optic Neuropathy: Update on Clinical Features and Current Therapeutic Approaches.

Chun BY, Rizzo JF 3rd.

Semin Pediatr Neurol. 2017 May;24(2):129-134. doi: 10.1016/j.spen.2017.06.001. Epub 2017 Jun 30. Review.

PMID:
28941528
5.

Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON).

Martins FTA, Miranda PMDAD, Fernandes MSA, Maciel-Guerra AT, Sartorato EL.

Mol Vis. 2017 Jul 21;23:495-503. eCollection 2017.

6.

The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy.

Majander A, Robson AG, João C, Holder GE, Chinnery PF, Moore AT, Votruba M, Stockman A, Yu-Wai-Man P.

Mitochondrion. 2017 Sep;36:138-149. doi: 10.1016/j.mito.2017.07.006. Epub 2017 Jul 18.

7.

Leber hereditary optic neuropathy: bridging the translational gap.

Jurkute N, Yu-Wai-Man P.

Curr Opin Ophthalmol. 2017 Sep;28(5):403-409. doi: 10.1097/ICU.0000000000000410. Review.

8.

Gene Therapy for Leber Hereditary Optic Neuropathy: Low- and Medium-Dose Visual Results.

Guy J, Feuer WJ, Davis JL, Porciatti V, Gonzalez PJ, Koilkonda RD, Yuan H, Hauswirth WW, Lam BL.

Ophthalmology. 2017 Nov;124(11):1621-1634. doi: 10.1016/j.ophtha.2017.05.016. Epub 2017 Jun 21.

PMID:
28647203
9.

Presymptomatic Visual Loss in Leber Hereditary Optic Neuropathy: A Therapeutic Window of Opportunity?

Chen JJ, Brodsky MC.

Ophthalmology. 2017 Jun;124(6):755-756. doi: 10.1016/j.ophtha.2017.02.030. No abstract available.

PMID:
28528823
10.

Vision Loss and Symmetric Basal Ganglia Lesions in Leber Hereditary Optic Neuropathy.

Mercuri MA, White H, Oliveira C.

J Neuroophthalmol. 2017 Dec;37(4):411-413. doi: 10.1097/WNO.0000000000000524.

PMID:
28459737
11.

Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy.

Wong RCB, Lim SY, Hung SSC, Jackson S, Khan S, Van Bergen NJ, De Smit E, Liang HH, Kearns LS, Clarke L, Mackey DA, Hewitt AW, Trounce IA, Pébay A.

Aging (Albany NY). 2017 Apr;9(4):1341-1350. doi: 10.18632/aging.101231.

12.

The Eye Drop Preservative Benzalkonium Chloride Potently Induces Mitochondrial Dysfunction and Preferentially Affects LHON Mutant Cells.

Datta S, Baudouin C, Brignole-Baudouin F, Denoyer A, Cortopassi GA.

Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2406-2412. doi: 10.1167/iovs.16-20903.

13.

Childhood-onset Leber hereditary optic neuropathy.

Majander A, Bowman R, Poulton J, Antcliff RJ, Reddy MA, Michaelides M, Webster AR, Chinnery PF, Votruba M, Moore AT, Yu-Wai-Man P.

Br J Ophthalmol. 2017 Nov;101(11):1505-1509. doi: 10.1136/bjophthalmol-2016-310072. Epub 2017 Mar 17.

14.

Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.

Wallace DC, Lott MT.

Handb Exp Pharmacol. 2017;240:339-376. doi: 10.1007/164_2017_2. Review.

PMID:
28233183
15.

Re: Feuer et al.: Gene therapy for Leber hereditary optic neuropathy: initial results (Ophthalmology 2016;123:558-570).

Dimopoulos IS, Xu M.

Ophthalmology. 2017 Mar;124(3):e22. doi: 10.1016/j.ophtha.2016.04.062. No abstract available.

PMID:
28219504
16.

Leber hereditary optic neuropathy due to a new ND1 mutation.

Soldath P, Wegener M, Sander B, Rosenberg T, Duno M, Wibrand F, Vissing J.

Ophthalmic Genet. 2017 Sep-Oct;38(5):480-485. doi: 10.1080/13816810.2016.1253108. Epub 2017 Jan 31.

PMID:
28139165
17.

Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy.

Yu-Wai-Man P, Soiferman D, Moore DG, Burté F, Saada A.

Mitochondrion. 2017 Sep;36:36-42. doi: 10.1016/j.mito.2017.01.004. Epub 2017 Jan 16.

18.

Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.

Li Y, Li J, Jia X, Xiao X, Li S, Guo X.

PLoS One. 2017 Jan 12;12(1):e0170090. doi: 10.1371/journal.pone.0170090. eCollection 2017.

19.

A Review of Mitochondrial Optic Neuropathies: From Inherited to Acquired Forms.

Pilz YL, Bass SJ, Sherman J.

J Optom. 2017 Oct - Dec;10(4):205-214. doi: 10.1016/j.optom.2016.09.003. Epub 2016 Dec 28. Review.

20.

Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T>C in MTND5.

Kolarova H, Liskova P, Tesarova M, Kucerova Vidrova V, Forgac M, Zamecnik J, Hansikova H, Honzik T.

Ophthalmic Genet. 2016 Dec;37(4):419-423. Epub 2016 Feb 19.

PMID:
26894521

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