Unilateral cone-rod dysfunction and retinal thinning in a child carrying the 14484 mutation of Leber hereditary optic neuropathy
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology and Child Health
Reference7 articles.
1. Hereditary optic neuropathies: from the mitochondria to the optic nerve;Newman;Am J Ophthalmol,2005
2. Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber’s hereditary optic neuropathy;Salomão;Doc Ophthalmol,2004
3. Outer retinal dysfunction in a patient with the 15257 mitochondrial DNA mutation;Fenton;Retin Cases Brief Rep,2011
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5. Reactive oxygen species in mitochondrial optic neuropathies: comment;Sadun;J Neuroophthalmol,2015
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases;Journal of Child Neurology;2023-01-19
2. Leber Hereditary Optic Neuropathy With Childhood Onset Producing Severe Unilateral Optic Neuropathy With No Relative Afferent Pupillary Defect;Journal of Neuro-Ophthalmology;2022-07-08
3. Cobalt toxic optic neuropathy and retinopathy: Case report and review of the literature;American Journal of Ophthalmology Case Reports;2020-03
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