1. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation. (3rd March 2020) Authors: Hosono, Katsuhiro; Kawase, Kazuhide; Kurata, Kentaro; Niimi, Yusuke; Saitsu, Hirotomo; Minoshima, Shinsei; Ohnishi, Hidenori; Yamamoto, Takahiro; Hikoya, Akiko; Tachibana, Nobutaka; Fukao, Toshiyuki; Yamamoto, Tetsuya; Hotta, Yoshihiro Journal: Ophthalmic genetics Issue: Volume 41:Number 2(2020) Page Start: 175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISK REGION. Issue 8 (August 2018) Authors: Yokoi, Tadashi; Katagiri, Satoshi; Hiraoka, Miina; Nakayama, Yuri; Hosono, Katsuhiro; Hotta, Yoshihiro; Nishina, Sachiko; Azuma, Noriyuki Journal: Retina Issue: Volume 38:Issue 8(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in the EYS Gene. (March 2014) Authors: Suto, Kimiko; Hosono, Katsuhiro; Takahashi, Masayo; Hirami, Yasuhiko; Arai, Yuki; Nagase, Yasunori; Ueno, Shinji; Terasaki, Hiroko; Minoshima, Shinsei; Kondo, Mineo; Hotta, Yoshihiro Journal: Ophthalmic genetics Issue: Volume 35:Number 1(2014:Mar.) Page Start: 25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Combination therapy of oncolytic herpes simplex virus HF10 and bevacizumab against experimental model of human breast carcinoma xenograft. Issue 7 (27th September 2014) Authors: Tan, Gewen; Kasuya, Hideki; Sahin, Tevfik Tolga; Yamamura, Kazuo; Wu, Zhiwen; Koide, Yusuke; Hotta, Yoshihiro; Shikano, Toshio; Yamada, Suguru; Kanzaki, Akiyuki; Fujii, Tsutomu; Sugimoto, Hiroyuki; Nomoto, Shuji; Nishikawa, Yoko; Tanaka, Maki; Tsurumaru, Naoko; Kuwahara, Toshie; Fukuda, Saori; Ic... Journal: International journal of cancer Issue: Volume 136:Issue 7(2015:Apr. 01) Page Start: 1718 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene. Issue 6 (1st June 2000) Authors: Hirano, Koji; Hotta, Yoshihiro; Fujiki, Keiko; Kanai, Atsushi Journal: British journal of ophthalmology Issue: Volume 84:Issue 6(2000) Page Start: 583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. De novo heterozygous variants in KIF5B cause kyphomelic dysplasia. Issue 1 (5th April 2022) Authors: Itai, Toshiyuki; Wang, Zheng; Nishimura, Gen; Ohashi, Hirofumi; Guo, Long; Wakano, Yasuhiro; Sugiura, Takahiro; Hayakawa, Hiromi; Okada, Mayumi; Saisu, Takashi; Kitta, Ayana; Doi, Hiroshi; Kurosawa, Kenji; Hotta, Yoshihiro; Hosono, Katsuhiro; Sato, Miho; Shimizu, Kenji; Takikawa, Kazuharu; Watana... Journal: Clinical genetics Issue: Volume 102:Issue 1(2022) Page Start: 3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Development of free piston engine linear generator system and a resonant pendulum type control method. (July 2021) Authors: Kosaka, Hidemasa; Akita, Tomoyuki; Goto, Shigeaki; Hotta, Yoshihiro Journal: International journal of engine research Issue: Volume 22:Number 7(2021) Page Start: 2254 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients. Issue 10 (17th June 2019) Authors: Koyanagi, Yoshito; Akiyama, Masato; Nishiguchi, Koji M; Momozawa, Yukihide; Kamatani, Yoichiro; Takata, Sadaaki; Inai, Chihiro; Iwasaki, Yusuke; Kumano, Mikako; Murakami, Yusuke; Omodaka, Kazuko; Abe, Toshiaki; Komori, Shiori; Gao, Dan; Hirakata, Toshiaki; Kurata, Kentaro; Hosono, Katsuhiro; Ueno... Journal: Journal of medical genetics Issue: Volume 56:Issue 10(2019) Page Start: 662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing. Issue 12 (7th November 2022) Authors: Suga, Akiko; Yoshitake, Kazutoshi; Minematsu, Naoko; Tsunoda, Kazushige; Fujinami, Kaoru; Miyake, Yozo; Kuniyoshi, Kazuki; Hayashi, Takaaki; Mizobuchi, Kei; Ueno, Shinji; Terasaki, Hiroko; Kominami, Taro; Nao‐I, Nobuhisa; Mawatari, Go; Mizota, Atsushi; Shinoda, Kei; Kondo, Mineo; Kato, Kumiko; Se... Journal: Human mutation Issue: Volume 43:Issue 12(2022) Page Start: 2251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of susceptibility loci for light-induced visual impairment in rats. (September 2021) Authors: Ohishi, Kentaro; Hosono, Katsuhiro; Obana, Akira; Noda, Akio; Hiramitsu, Tadahisa; Hotta, Yoshihiro; Minoshima, Shinsei Journal: Experimental eye research Issue: Volume 210(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗