CHANGES OF CONE PHOTORECEPTOR MOSAIC IN AUTOSOMAL RECESSIVE BESTROPHINOPATHY-Reference-Cited by-同舟云学术

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CHANGES OF CONE PHOTORECEPTOR MOSAIC IN AUTOSOMAL RECESSIVE BESTROPHINOPATHY

Published:2020-01 Issue:1 Volume:40 Page:181-186
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Nakanishi Ayami,Ueno Shinji,Hayashi Takaaki,Katagiri Satoshi,Ito Yasuki,Kominami Taro,Fujinami Kaoru,Tsunoda Kazushige,Iwata Takeshi,Terasaki Hiroko

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference15 articles.

1. Biallelic mutation of BEST1 causes a distinct retinopathy in humans;Burgess;Am J Hum Genet,2008

2. Identification of the gene responsible for Best macular dystrophy;Petrukhin;Nat Genet,1998

3. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options;Boon;Ophthalmology,2013

4. Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patients;Kinnick;Retina,2011

5. Clinical and genetic findings of autosomal recessive bestrophinopathy in Japanese cohort;Nakanishi;Am J Ophthalmol,2016

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1. Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights;Scientific Reports;2024-07-04

2. Adaptive optics imaging in inherited retinal diseases: A scoping review of the clinical literature;Survey of Ophthalmology;2024-01

3. Photoreceptor function and structure in retinal degenerations caused by biallelic BEST1 mutations;Vision Research;2023-02

4. Twelve-year follow up of a case of autosomal recessive bestrophinopathy with transient resolution of retinal edema in one eye;European Journal of Ophthalmology;2022-01-06

5. Clinical findings in eyes with BEST1-related retinopathy complicated by choroidal neovascularization;Graefe's Archive for Clinical and Experimental Ophthalmology;2021-10-18

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