小児の網膜電図記録用に新しく試作した極小LED内蔵コンタクトレンズ電極の使用経験
永濱 皆美, 奥 一真, 近藤 寛之
あたらしい眼科, Jul. 2021, Reviewed, No invitation

自動車運転が課題となった脳梗塞後の半盲の一例
村上 美紀, 奥 一真, 蜂須賀 研二, 近藤 寛之
日本ロービジョン学会誌, Mar. 2019, Reviewed, Null

アトピー性皮膚炎患者に対する硝子体手術施行例の外眼部所見
成瀬 翔, 近藤 寛之, 奥 一真, 森田 啓文
眼科臨床紀要, May 2018, Reviewed, Null

水晶体亜脱臼を伴う低眼圧症に対し、眼内レンズ毛様溝縫着術が奏効した3例
奥 一真, 真野 奈津子, 喜田 照代, 池田 恒彦, 近藤 寛之
眼科臨床紀要, Mar. 2017, Reviewed, Null
Lead

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.
Kondo Hiroyuki, Oku Kazuma, Katagiri Satoshi, Hayashi Takaaki, Nakano Tadashi, Iwata Akiko, Kuniyoshi Kazuki, Kusaka Shunji, Hiyoshi Atsushi, Uchio Eiichi, Kondo Mineo, Oishi Noriko, Kameya Shuhei, Mizota Atsushi, Naoi Nobuhisa, Ueno Shinji, Terasaki Hiroko, Morimoto Takeshi, Iwaki Masayoshi, Yoshitake Kazutoshi, Iejima Daisuke, Fujinami Kaoru, Tsunoda Kazushige, Shinoda Kei, Iwata Takeshi
Human genome variation, Jan. 2019, Reviewed, Null

Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015)
Kazuma Oku, Kei Tokutsu, Shinya Matsuda, Hiroyuki Kondo
Japanese Journal of Ophthalmology, Aug. 2021, Reviewed, Null
Lead

Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene
Mamika Asano_x000D_ Katsuhiko Yokoyama_x000D_ Kazuma Oku_x000D_ Itsuka Matsushita_x000D_ Kenichi Kimoto_x000D_ Toshiaki Kubota_x000D_ Hiroyuki Kondo
Ophthalmic genetics, Apr. 2022, Reviewed, No invitation

ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME.
Fujimoto Kazushi, Nagata Tatsuo, Matsushita Itsuka, Oku Kazuma, Imagawa Mamika, Kuniyoshi Kazuki, Hayashi Takaaki, Kimoto Kenichi, Ohji Masahito, Kusaka Shunji, Kondo Hiroyuki
Retina (Philadelphia, Pa.), Mar. 2021, Reviewed, No invitation