1. CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family. (4th July 2018) Authors: Kubota, Daiki; Gocho, Kiyoko; Kikuchi, Sachiko; Akeo, Keiichiro; Miura, Masahiro; Yamaki, Kunihiko; Takahashi, Hiroshi; Kameya, Shuhei Journal: Ophthalmic genetics Issue: Volume 39:Number 4(2018) Page Start: 500 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cone Dystrophy in Patient with Homozygous RP1L1 Mutation. (29th January 2015) Authors: Kikuchi, Sachiko; Kameya, Shuhei; Gocho, Kiyoko; El Shamieh, Said; Akeo, Keiichiro; Sugawara, Yuko; Yamaki, Kunihiko; Zeitz, Christina; Audo, Isabelle; Takahashi, Hiroshi Other Names: Mizota Atsushi Academic Editor. Journal: BioMed research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera. (18th August 2015) Authors: Akeo, Keiichiro; Kameya, Shuhei; Gocho, Kiyoko; Kubota, Daiki; Yamaki, Kunihiko; Takahashi, Hiroshi Other Names: Lombardo Marco Academic Editor. Journal: Case reports in ophthalmological medicine Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy. (28th November 2013) Authors: Gocho, Kiyoko; Kikuchi, Sachiko; Kabuto, Takenori; Kameya, Shuhei; Shinoda, Kei; Mizota, Atsushi; Yamaki, Kunihiko; Takahashi, Hiroshi Other Names: Votruba Marcela Academic Editor. Journal: BioMed research international Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation. (3rd September 2014) Authors: Gocho, Kiyoko; Kameya, Shuhei; Akeo, Keiichiro; Kikuchi, Sachiko; Usui, Ayumi; Yamaki, Kunihiko; Hayashi, Takaaki; Tsuneoka, Hiroshi; Mizota, Atsushi; Takahashi, Hiroshi Other Names: Lai Timothy Y. Academic Editor. Journal: Journal of ophthalmology Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation. (1st November 2020) Authors: Kubota, Daiki; Matsumoto, Kaori; Hayashi, Mika; Oishi, Noriko; Gocho, Kiyoko; Yamaki, Kunihiko; Kobayakawa, Shinichiro; Igarashi, Tsutomu; Takahashi, Hiroshi; Kameya, Shuhei Journal: Ophthalmic genetics Issue: Volume 41:Number 6(2020) Page Start: 629 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation. (4th May 2021) Authors: Oishi, Noriko; Kubota, Daiki; Nakamoto, Kenji; Takeda, Yukito; Hayashi, Mika; Gocho, Kiyoko; Yamaki, Kunihiko; Igarashi, Tsutomu; Takahashi, Hiroshi; Kameya, Shuhei Journal: Ophthalmic genetics Issue: Volume 42:Number 3(2021) Page Start: 304 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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. (3rd September 2019) Authors: Kubota, Daiki; Oishi, Noriko; Gocho, Kiyoko; Kikuchi, Sachiko; Yamaki, Kunihiko; Igarashi, Tsutomu; Takahashi, Hiroshi; Ishida, Nobuo; Iwata, Takeshi; Mizota, Atsushi; Kameya, Shuhei Journal: Ophthalmic genetics Issue: Volume 40:Number 5(2019) Page Start: 480 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗