Foveal Cone Electroretinograms in Patients With Central Visual Loss of Unexplained Etiology
Author:
Publisher
American Medical Association (AMA)
Subject
Ophthalmology
Cited by 27 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. Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene;Molecular Medicine Reports;2016-01-14
2. Transient, Unexplained, and Psychogenic Visual Loss in Children;Pediatric Neuro-Ophthalmology;2016
3. Multimodal Approach to Monitoring and Investigating Cone Structure and Function in an Inherited Macular Dystrophy;American Journal of Ophthalmology;2015-08
4. Cone Dystrophy in Patient with HomozygousRP1L1Mutation;BioMed Research International;2015
5. Fundus Autofluorescence in Autosomal Dominant Occult Macular Dystrophy;Archives of Ophthalmology;2011-05-09
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