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Research article

First published 2012-10

Optic Atrophy Differentially Diagnosed as Spinocerebellar Ataxia from Leber Hereditary Optic Neuropathy by Gene Mutation Analysis

YP Song, ZS Chen, GY Mo [...]

Journal of International Medical Research

Free access

Meeting report

First published 1935-8

A Pedigree of Congenital Optic Atrophy Embracing Sixteen Affected Cases in Six Generations

A. Hugh Thompson, G. T. Willoughby Cashell

Journal of the Royal Society of Medicine

Open access

Review article

First published 2017

Use of Idebenone for the Treatment of Leber’s Hereditary Optic Neuropathy

Claudia B. Catarino, Thomas Klopstock

Journal of Inborn Errors of Metabolism and Screening

Open access

Review article

First published 2021

New avenues for therapy in mitochondrial optic neuropathies

Wing Sum Vincent Ng, Matthieu Trigano, Thomas Freeman [...]

Therapeutic Advances in Rare Disease

Retricted access

Research article

First published 1997-01

Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis

Bernadette Kalman, Jose Luis Rodriguez-Valdez, Ursula Bosch [...]

Multiple Sclerosis Journal

Open access

Review article

First published 2020

OCTA in neurodegenerative optic neuropathies: emerging biomarkers at the eye–brain interface

Samuel Asanad, Isa Mohammed, Alfredo A. Sadun [...]

Therapeutic Advances in Ophthalmology

Open access

Case report

First published 2023-11

RPGRIP1 variant associated with pigmented paravenous chorioretinal atrophy

Lorenzo Bianco, Alessio Antropoli, Alessandro Arrigo [...]

European Journal of Ophthalmology

Retricted access

Research article

First published 2025-7

Causes of Blindness and Low Vision in Schools for Students With Visual Impairments in Tehran

Hamid Ahmadieh, Narsis Daftarian, Mojtaba Rajabpour [...]

Journal of Visual Impairment & Blindness

Retricted access

Research article

First published 2016-1

Leber Congenital Amaurosis: First Genotyped Hungarian Patients and Report of 2 Novel Mutations in the CRB1 and CEP290 Genes

Rita Vámos, Maigi Külm, Viktoria Szabó [...]

European Journal of Ophthalmology

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