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ArticlesPeer ReviewedFull Text
New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome
Author / Creator:Kuniyoshi, Kazuki ; Hayashi, Takaaki ; Sakuramoto, Hiroyuki ; Mishima, Hiroshi ; Tsuneoka, Hiroshi ; Tsunoda, Kazushige ; Iwata, Takeshi ; Shimomura, Yoshikazu
Publisher:Tokyo: Springer Japan
Journal title:Japanese journal of ophthalmology, 2016-11, Vol.60 (6), p.476-485
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ArticlesPeer ReviewedFull Text
Intravitreal injection of bevacizumab for retinopathy of prematurity
Author / Creator:Kuniyoshi, Kazuki ; Sugioka, Koji ; Sakuramoto, Hiroyuki ; Kusaka, Shunji ; Wada, Norihisa ; Shimomura, Yoshikazu
Publisher:Tokyo: Springer Japan
Journal title:Japanese journal of ophthalmology, 2014-05, Vol.58 (3), p.237-243
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ArticlesPeer ReviewedFull Text
Two types of acute zonal occult outer retinopathy differentiated by dark- and light-adapted perimetry
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Nakao, Yuzo ; Matsumoto, Chota ; Shimomura, Yoshikazu
Publisher:Tokyo: Springer Japan
Journal title:Japanese journal of ophthalmology, 2014-03, Vol.58 (2), p.177-187
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ArticlesPeer ReviewedFull Text
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia
Author / Creator:Kuniyoshi, Kazuki ; Muraki-Oda, Sanae ; Ueyama, Hisao ; Toyoda, Futoshi ; Sakuramoto, Hiroyuki ; Ogita, Hisakazu ; Irifune, Motohiro ; Yamamoto, Shuji ; Nakao, Akira ; Tsunoda, Kazushige ; Iwata, Takeshi ; Ohji, Masahito ; Shimomura, Yoshikazu
Publisher:Tokyo: Springer Japan
Journal title:Japanese journal of ophthalmology, 2016-05, Vol.60 (3), p.187-197
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ArticlesPeer ReviewedFull Text
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy
Author / Creator:Kuniyoshi, Kazuki ; Hayashi, Takaaki ; Kameya, Shuhei ; Katagiri, Satoshi ; Mizobuchi, Kei ; Tachibana, Toshiaki ; Kubota, Daiki ; Sakuramoto, Hiroyuki ; Tsunoda, Kazushige ; Fujinami, Kaoru ; Yoshitake, Kazutoshi ; Iwata, Takeshi ; Nakano, Tadashi ; Kusaka, Shunji
Publisher:Switzerland: MDPI
Journal title:International journal of molecular sciences, 2020-02, Vol.21 (4), p.1331
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ArticlesPeer ReviewedFull Text
Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Yoshitake, Kazutoshi ; Abe, Kosuke ; Ikeo, Kazuho ; Furuno, Masaaki ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2014-06, Vol.128 (3), p.219-228
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ArticlesPeer ReviewedFull Text
Long-lasting, dense scotoma under light-adapted conditions in patient with multiple evanescent white dot syndrome
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Sugioka, Koji ; Matsumoto, Chota ; Kusaka, Shunji ; Shimomura, Yoshikazu
Publisher:Dordrecht: Springer Netherlands
Journal title:International ophthalmology, 2016-08, Vol.36 (4), p.601-605
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ArticlesPeer ReviewedFull Text
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Yoshitake, Kazutoshi ; Ikeo, Kazuho ; Furuno, Masaaki ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2015-08, Vol.131 (1), p.71-79
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ArticlesPeer ReviewedFull Text
Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy
Author / Creator:Kuniyoshi, Kazuki ; Ikeo, Kazuho ; Sakuramoto, Hiroyuki ; Furuno, Masaaki ; Yoshitake, Kazutoshi ; Hatsukawa, Yoshikazu ; Nakao, Akira ; Tsunoda, Kazushige ; Kusaka, Shunji ; Shimomura, Yoshikazu ; Iwata, Takeshi
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Documenta ophthalmologica, 2015-02, Vol.130 (1), p.49-55
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ArticlesPeer ReviewedFull Text
A case of bilateral, acquired, and acute dysfunction of short-wavelength-sensitive cone systems
Author / Creator:Kuniyoshi, Kazuki ; Sakuramoto, Hiroyuki ; Nakao, Akira ; Takada, Sonoko ; Shimomura, Yoshikazu
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Documenta ophthalmologica, 2012-08, Vol.125 (1), p.75-80
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ArticlesPeer ReviewedFull Text
Novel mutations in the gene for [alpha]-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia
Author / Creator:Kuniyoshi, Kazuki ; Muraki-oda, Sanae ; Ueyama, Hisao ; Toyoda, Futoshi ; Sakuramoto, Hiroyuki ; Ogita, Hisakazu ; Irifune, Motohiro ; Yamamoto, Shuji ; Nakao, Akira ; Tsunoda, Kazushige ; Iwata, Takeshi ; Ohji, Masahito ; Shimomura, Yoshikazu
Publisher:Tokyo: Springer Nature B.V
Journal title:Japanese journal of ophthalmology, 2016-05, Vol.60 (3), p.187
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ArticlesPeer ReviewedFull Text
Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration
Author / Creator:Sakuramoto, Hiroyuki ; Kuniyoshi ; Tsunoda ; Akahori ; Iwata ; Shimomura
Publisher:New Zealand: Taylor & Francis Ltd
Journal title:Clinical ophthalmology (Auckland, N.Z.), 2013-01, Vol.7 (default), p.1703-1711
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ReportsFull Text
Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration
Author / Creator:Sakuramoto, Hiroyuki ; Kuniyoshi, Kazuki ; Tsunoda, Kazushige ; Akahori, Masakazu ; Iwata, Takeshi ; Shimomura, Yoshikazu
Journal title:Clinical ophthalmology (Auckland, N.Z.), 2013, Vol.7, p.1703-1711
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ArticlesPeer ReviewedFull Text
Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques
Author / Creator:Fujinami-Yokokawa, Yu ; Ninomiya, Hideki ; Liu, Xiao ; Yang, Lizhu ; Pontikos, Nikolas ; Yoshitake, Kazutoshi ; Iwata, Takeshi ; Sato, Yasunori ; Hashimoto, Takeshi ; Tsunoda, Kazushige ; Miyata, Hiroaki ; Fujinami, Kaoru
Publisher:England: BMJ Publishing Group LTD
Journal title:British journal of ophthalmology, 2021-09, Vol.105 (9), p.1272-1279
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New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome

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Intravitreal injection of bevacizumab for retinopathy of prematurity

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Two types of acute zonal occult outer retinopathy differentiated by dark- and light-adapted perimetry

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Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia

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Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy

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Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation

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Long-lasting, dense scotoma under light-adapted conditions in patient with multiple evanescent white dot syndrome

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Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations

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Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy

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A case of bilateral, acquired, and acute dysfunction of short-wavelength-sensitive cone systems

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Novel mutations in the gene for [alpha]-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia

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Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration

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Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration

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Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques

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