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Meeting Abstract (6)
Journal Articles (4)

Journal

Investigative Ophthalmology & Visual Science (10)

Article Type

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

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Eye Anatomy and Disorders (4)
Genetics (4)
Retina (4)
Imaging (1)

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cohort studies (3)
japanese (3)
eye (2)
macular dystrophy (2)
ophthalmoscopy (2)
photoreceptors (2)
retinal diseases (2)
cone dystrophy (1)
electroretinography (1)
family (1)

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Retina March 2020

RDH5 -Related Fundus Albipunctatus in a Large Japanese Cohort

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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. doi: 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

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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. doi: 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

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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. doi: 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. doi: https://doi.org/

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. doi: https://doi.org/

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. doi: https://doi.org/

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. doi: https://doi.org/

Genetics September 2016

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

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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: phenotype, cohort studies, family, genes, genotype, photoreceptors, retinal diseases, macular dystrophy, japanese, whole exome sequencing
Invest. Ophthalmol. Vis. Sci.. 2016; 57(11):4837-4846. doi: 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. doi: https://doi.org/

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. doi: https://doi.org/

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Online ISSN: 1552-5783

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

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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