Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families
Hayashi, Takaaki, Kameya, Shuhei, Mizobuchi, Kei, Kubota, Daiki, Kikuchi, Sachiko, Yoshitake, Kazutoshi, Mizota, Atsushi, Murakami, Akira, Iwata, Takeshi, Nakano, Tadashi
Published in Scientific reports (28.09.2020)
Published in Scientific reports (28.09.2020)
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An effective strategy to reduce blood pressure after forest walking in middle-aged and aged people
Horiuchi, Masahiro, Endo, Junko, Akatsuka, Shin, Hasegawa, Tatsuya, Yamamoto, Eriko, Uno, Tadashi, Kikuchi, Sachiko
Published in Journal of Physical Therapy Science (2015)
Published in Journal of Physical Therapy Science (2015)
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High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia
Suzuki, Kai, Gocho, Kiyoko, Akeo, Keiichiro, Kikuchi, Sachiko, Kubota, Daiki, Katagiri, Satoshi, Fujinami, Kaoru, Tsunoda, Kazushige, Iwata, Takeshi, Yamaki, Kunihiko, Igarashi, Tsutomu, Nakano, Tadashi, Takahashi, Hiroshi, Hayashi, Takaaki, Kameya, Shuhei
Published in Ophthalmic surgery, lasers & imaging (01.02.2019)
Published in Ophthalmic surgery, lasers & imaging (01.02.2019)
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Multimodal imaging of a case of peripheral cone dystrophy
Ito, Naoko, Kameya, Shuhei, Gocho, Kiyoko, Hayashi, Takaaki, Kikuchi, Sachiko, Katagiri, Satoshi, Gekka, Tamaki, Yamaki, Kunihiko, Takahashi, Hiroshi, Tsuneoka, Hiroshi
Published in Documenta ophthalmologica (01.06.2015)
Published in Documenta ophthalmologica (01.06.2015)
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High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation
Takahashi, Hiroshi, Mizota, Atsushi, Hayashi, Takaaki, Yamaki, Kunihiko, Usui, Ayumi, Kikuchi, Sachiko, Akeo, Keiichiro, Kameya, Shuhei, Gocho, Kiyoko, Tsuneoka, Hiroshi
Published in Journal of Ophthalmology (01.01.2014)
Published in Journal of Ophthalmology (01.01.2014)
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Limbal nodules associated with Sweet’s syndrome
Kikuchi, Sachiko, Hori, Junko, Tsukada, Reiko, Takahashi, Hiroshi, Kato, Tokue
Published in Japanese journal of ophthalmology (01.11.2009)
Published in Japanese journal of ophthalmology (01.11.2009)
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Journal Article
CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family
Kubota, Daiki, Gocho, Kiyoko, Kikuchi, Sachiko, Akeo, Keiichiro, Miura, Masahiro, Yamaki, Kunihiko, Takahashi, Hiroshi, Kameya, Shuhei
Published in Ophthalmic genetics (01.08.2018)
Published in Ophthalmic genetics (01.08.2018)
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Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy
Fujinami, Kaoru, Kameya, Shuhei, Kikuchi, Sachiko, Ueno, Shinji, Kondo, Mineo, Hayashi, Takaaki, Shinoda, Kei, Machida, Shigeki, Kuniyoshi, Kazuki, Kawamura, Yuichi, Akahori, Masakazu, Yoshitake, Kazutoshi, Katagiri, Satoshi, Nakanishi, Ayami, Sakuramoto, Hiroyuki, Ozawa, Yoko, Tsubota, Kazuo, Yamaki, Kunihiko, Mizota, Atsushi, Terasaki, Hiroko, Miyake, Yozo, Iwata, Takeshi, Tsunoda, Kazushige
Published in Investigative ophthalmology & visual science (01.09.2016)
Published in Investigative ophthalmology & visual science (01.09.2016)
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Journal Article
Brian Friel's Search for Irishness in Dancing at Lughnasa and Wonderful Tennessee
KIKUCHI, Sachiko
Published in Eibeibunka: Studies in English Language, Literature and Culture (31.03.2009)
Published in Eibeibunka: Studies in English Language, Literature and Culture (31.03.2009)
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Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variants
Kominami, Azusa, Ueno, Shinji, Kominami, Taro, Nakanishi, Ayami, Ito, Yasuki, Fujinami, Kaoru, Tsunoda, Kazushige, Hayashi, Takaaki, Kikuchi, Sachiko, Kameya, Shuhei, Iwata, Takeshi, Terasaki, Hiroko
Published in Ophthalmic genetics (01.04.2018)
Published in Ophthalmic genetics (01.04.2018)
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Journal Article
High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy
Takahashi, Hiroshi, Mizota, Atsushi, Shinoda, Kei, Kameya, Shuhei, Kabuto, Takenori, Kikuchi, Sachiko, Gocho, Kiyoko, Yamaki, Kunihiko
Published in BioMed research international (01.01.2013)
Published in BioMed research international (01.01.2013)
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Journal Article
Cone Dystrophy in Patient with Homozygous RP1L1 Mutation
Takahashi, Hiroshi, Audo, Isabelle, Yamaki, Kunihiko, Sugawara, Yuko, Akeo, Keiichiro, El Shamieh, Said, Gocho, Kiyoko, Kameya, Shuhei, Kikuchi, Sachiko, Zeitz, Christina
Published in BioMed research international (01.01.2015)
Published in BioMed research international (01.01.2015)
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Journal Article
Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family
Kubota, Daiki, Oishi, Noriko, Gocho, Kiyoko, Kikuchi, Sachiko, Yamaki, Kunihiko, Igarashi, Tsutomu, Takahashi, Hiroshi, Ishida, Nobuo, Iwata, Takeshi, Mizota, Atsushi, Kameya, Shuhei
Published in Ophthalmic genetics (03.09.2019)
Published in Ophthalmic genetics (03.09.2019)
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Journal Article
Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation
Kubota, Daiki, Gocho, Kiyoko, Akeo, Keiichiro, Kikuchi, Sachiko, Sugahara, Michitaka, Matsumoto, Celso Soiti, Shinoda, Kei, Mizota, Atsushi, Yamaki, Kunihiko, Takahashi, Hiroshi, Kameya, Shuhei
Published in Documenta ophthalmologica (01.06.2016)
Published in Documenta ophthalmologica (01.06.2016)
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