Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Author:
Publisher
S. Karger AG
Subject
Sensory Systems,Ophthalmology,General Medicine
Reference29 articles.
1. Contributions of Genetics to Our Understanding of Inherited Monogenic Retinal Diseases and Age-Related Macular Degeneration
2. The human visual cortex responds to gene therapy–mediated recovery of retinal function
3. Gene Therapy for Leber Congenital Amaurosis
4. Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success
5. Why Some Photoreceptors Die, While Others Remain Dormant: Lessons FromRPE65andLRATAssociated Retinal Dystrophies
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1. Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation Sequencing;International Journal of Molecular Sciences;2022-01-17
2. Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy;Clinical Ophthalmology;2021-12
3. An optometrist’s guide to the top candidate inherited retinal diseases for gene therapy;Clinical and Experimental Optometry;2021-02-25
4. Melanopsin hypersensitivity dominates interictal photophobia in migraine;Cephalalgia;2020-10-12
5. Early onset retinal dystrophies: clinical clues to diagnosis for pediatricians;Italian Journal of Pediatrics;2019-12
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