Search | IOVS | ARVO Journals

iovs

Issues
Topics
For Authors
About
- Editorial Board

Journals Home

MANAGE ALERTS

Access Provided By:
MIT Libraries

Forgot password?

Create an Account

To View More...

Purchase this article with an account.

or

Subscribe Now

Issues
Topics
For Authors
About
- Editorial Board

Narrow View

NARROW

Content Type

Meeting Abstract (6)
Journal Articles (5)

Journal

Investigative Ophthalmology & Visual Science (10)
Translational Vision Science & Technology (1)

Article Type

ARVO Annual Meeting Abstract (5)
Genetics (2)
Retina (2)
ARVO Imaging in the Eye Conference Abstract (1)
Articles (1)

Topics

Eye Anatomy and Disorders (5)
Genetics (5)
Retina (5)
Imaging (1)
Translational Research (1)

Tags

cohort studies (4)
eye (3)
japanese (3)
retinal diseases (3)
family (2)
macular dystrophy (2)
ophthalmoscopy (2)
phenotype (2)
photoreceptors (2)
visual acuity (2)

Specify Date Range

From: To: Apply

Showing 1 – 11 of 11

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

Articles May 2020

Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with GUCY2D -Associated Retinal Disorder

PDF

Xiao Liu; Kaoru Fujinami; Kazuki Kuniyoshi; Mineo Kondo; Shinji Ueno; Takaaki Hayashi; Kiyofumi Mochizuki; Shuhei Kameya; Lizhu Yang; Yu Fujinami-Yokokawa; Gavin Arno; Nikolas Pontikos; Hiroyuki Sakuramoto; Taro Kominami; Hiroko Terasaki; Satoshi Katagiri; Kei Mizobuchi; Natsuko Nakamura; Kazutoshi Yoshitake; Yozo Miyake; Shiying Li; Toshihide Kurihara; Kazuo Tsubota; Takeshi Iwata; Kazushige Tsunoda; Japan Eye Genetics Consortium
TAGS: cohort studies, family, genetics, japanese, retinal diseases, phenotype, eye, visual acuity
Trans. Vis. Sci. Tech.. 2020; 9(6):2. https://doi.org/10.1167/tvst.9.6.2

Includes: Supplemental Content

Retina March 2020

RDH5 -Related Fundus Albipunctatus in a Large Japanese Cohort

PDF

Satoshi Katagiri; Takaaki Hayashi; Masaki Nakamura; Kei Mizobuchi; Tamaki Gekka; Shiori Komori; Shinji Ueno; Hiroko Terasaki; Hiroyuki Sakuramoto; Kazuki Kuniyoshi; Shunji Kusaka; Ryunosuke Nagashima; Mineo Kondo; Kaoru Fujinami; Kazushige Tsunoda; Tomokazu Matsuura; Hiroyuki Kondo; Kazutoshi Yoshitake; Takeshi Iwata; Tadashi Nakano
TAGS: cohort studies, japanese, pigmentary retinal dystrophy, electroretinography, eye, ophthalmoscopy, genetic pedigree, retinal cone
Invest. Ophthalmol. Vis. Sci.. 2020; 61(3):53. https://doi.org/10.1167/iovs.61.3.53

Includes: Supplemental Content

Retina November 2019

Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings

PDF

Natsuko Nakamura; Kazushige Tsunoda; Yoshinobu Mizuno; Tomoaki Usui; Tetsuhisa Hatase; Shinji Ueno; Kazuki Kuniyoshi; Takaaki Hayashi; Satoshi Katagiri; Mineo Kondo; Shuhei Kameya; Kazutoshi Yoshitake; Kaoru Fujinami; Takeshi Iwata; Yozo Miyake
TAGS: macular dystrophy, optical coherence tomography, visual acuity, visual symptoms, survival curve, photoreceptors, symptom onset
Invest. Ophthalmol. Vis. Sci.. 2019; 60(14):4691-4700. https://doi.org/10.1167/iovs.19-27486

Genetics August 2019

Phenotypical Characteristics of POC1B -Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance

PDF

Shuhei Kameya; Kaoru Fujinami; Shinji Ueno; Takaaki Hayashi; Kazuki Kuniyoshi; Ryuichi Ideta; Sachiko Kikuchi; Daiki Kubota; Kazutoshi Yoshitake; Satoshi Katagiri; Hiroyuki Sakuramoto; Taro Kominami; Hiroko Terasaki; Lizhu Yang; Yu Fujinami-Yokokawa; Xiao Liu; Gavin Arno; Nikolas Pontikos; Yozo Miyake; Takeshi Iwata; Kazushige Tsunoda; for the Japan Eye Genetics Consortium
TAGS: cohort studies, cone dystrophy, eye, japanese, ophthalmology, ophthalmoscopy, retinal diseases, universities, spectral domain-optical coherence tomography, mutation
Invest. Ophthalmol. Vis. Sci.. 2019; 60(10):3432-3446. https://doi.org/10.1167/iovs.19-26650

Includes: Supplemental Content

ARVO Imaging in the Eye Conference Abstract August 2019

High resolution adaptive optics imaging analysis of Enhanced S-Cone syndrome with NR2E3 mutation

Kiyoko Gocho; Kazuki Kuniyoshi; Takaaki Hayashi; Satoshi Katagiri; Daiki Kubota; Hiroshi Takahashi; Shuhei Kameya

Invest. Ophthalmol. Vis. Sci.. 2019; 60(11):PB0142.

ARVO Annual Meeting Abstract July 2018

Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing

Katsuhiro Hosono; Sachiko Nishina; Tadashi Yokoi; Satoshi Katagiri; Kentaro Kurata; Daisuke Miyamichi; Kei Mizobuchi; Tadashi Nakano; Shinsei Minoshima; Maki Fukami; Hiroyuki Kondo; Miho Sato; Takaaki Hayashi; Noriyuki Azuma; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5414.

ARVO Annual Meeting Abstract June 2017

High resolution imaging analysis of female carriers and patients of choroideremia with CHM gene mutation

Kiyoko Gocho; Keiichiro Akeo; Daiki Kubota; Satoshi Katagiri; Sachiko Kikuchi; Takaaki Hayashi; Kunihiko Yamaki; Hiroshi Takahashi; Shuhei Kameya

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):307.

ARVO Annual Meeting Abstract September 2016

Diminished density of cone photoreceptors in fovea of eyes with autosomal recessive bestrophinopathy

Ayami Nakanishi; Shinji Ueno; Taro Kominami; Yasuki Ito; Takaaki Hayashi; Satoshi Katagiri; Takeshi Iwata; Hiroko Terasaki

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):5107.

Genetics September 2016

Novel RP1L1 Variants and Genotype–Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy

PDF

Kaoru Fujinami; Shuhei Kameya; Sachiko Kikuchi; Shinji Ueno; Mineo Kondo; Takaaki Hayashi; Kei Shinoda; Shigeki Machida; Kazuki Kuniyoshi; Yuichi Kawamura; Masakazu Akahori; Kazutoshi Yoshitake; Satoshi Katagiri; Ayami Nakanishi; Hiroyuki Sakuramoto; Yoko Ozawa; Kazuo Tsubota; Kunihiko Yamaki; Atsushi Mizota; Hiroko Terasaki; Yozo Miyake; Takeshi Iwata; Kazushige Tsunoda
TAGS: cohort studies, genes, genotype, macular dystrophy, phenotype, photoreceptors, family, retinal diseases
Invest. Ophthalmol. Vis. Sci.. 2016; 57(11):4837-4846. https://doi.org/10.1167/iovs.16-19670

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

Biallelic mutation of BEST1 causes ARB with varying degrees of severity in two Japanese families.

Ayami Nakanishi; Shinji Ueno; Takaaki Hayashi; Satoshi Katagiri; Takeshi Iwata; Hiroko Terasaki

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2335.

ARVO Annual Meeting Abstract April 2014

BEST1 mutations in Japanese patients with Best vitelliform macular dystrophy

Satoshi Katagiri; Takaaki Hayashi; Tetsuju Sekiryu; Tamaki Gekka; Masakazu Akahori; Hiroyuki Sasano; Yasuhiro Ohkuma; Takeshi Iwata; Hiroshi Tsuneoka

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3258.

« Previous

Advertisement

Follow @ARVOiovs

IOVS Home
Issues
Topics
For Authors
About
- Editorial Board

Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

JOURNALS HOME
TOPICS
ABOUT ARVO JOURNALS

Copyright © 2025 Association for Research in Vision and Ophthalmology.

Access Provided By:
MIT Libraries

Forgot password?

To View More...

Purchase this article with an account.

Create an Account

or

Subscribe Now

×

×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×

This site uses cookies. By continuing to use our website, you are agreeing to our privacy policy.Accept