Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments

por Kondo, Hiroyuki
Publicado en Taiwan J Ophthalmol (2015)

Foveal hypoplasia and optical coherence tomographic imaging

por Kondo, Hiroyuki
Publicado en Taiwan J Ophthalmol (2018)

Efficacy and safety of rotigotine in elderly patients with Parkinson’s disease in comparison with the non-elderly: a post hoc analysis of randomized, double-blind, placebo-controll...

por Nomoto, Masahiro, Iwaki, Hirotaka, Kondo, Hiroyuki, Sakurai, Masaya
Publicado en J Neurol (2017)

Correction to: Efficacy and safety of rotigotine in elderly patients with Parkinson’s disease in comparison with the non-elderly: a post hoc analysis of randomized, double-blind, p...

por Nomoto, Masahiro, Iwaki, Hirotaka, Kondo, Hiroyuki, Sakurai, Masaya
Publicado en J Neurol (2017)

Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy

por Asano, Mamika, Tsukamoto, Shoko, Sonoda, Koh-Hei, Kondo, Hiroyuki
Publicado en Am J Ophthalmol Case Rep (2021)

Early vitrectomy to reverse macular dragging in a one-month-old boy with familial exudative vitreoretinopathy

por Iwata, Akiko, Kusaka, Shunji, Ishimaru, Mayumi, Kondo, Hiroyuki, Kuniyoshi, Kazuki
Publicado en Am J Ophthalmol Case Rep (2019)

Polyethylene Glycol-Based Synthetic Hydrogel Sealant for Filtration Bleb Leaks: An In Vivo and Histologic Study

por Nagata, Tatsuo, Harada, Yukinori, Arai, Mikki, Hirose, Tatsuo, Kondo, Hiroyuki
Publicado en Transl Vis Sci Technol (2020)

Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity

por Kondo, Hiroyuki, Kusaka, Shunji, Yoshinaga, Aki, Uchio, Eiichi, Tawara, Akihiko, Tahira, Tomoko
Publicado 2013

Thymoproteasomes produce unique peptide motifs for positive selection of CD8(+) T cells

por Sasaki, Katsuhiro, Takada, Kensuke, Ohte, Yuki, Kondo, Hiroyuki, Sorimachi, Hiroyuki, Tanaka, Keiji, Takahama, Yousuke, Murata, Shigeo
Publicado en Nat Commun (2015)

Effectiveness of Mammographic Screening for Breast Cancer in Women Aged over 50 Years in Japan

por Morimoto, Tadaoki, Sasa, Mitsunori, Yamaguchi, Tetsuo, Kondo, Hiroyuki, Sagara, Yasunobu, Kuwamura, Yumi, Yamamoto, Sumiko, Tada, Toshiko
Publicado en Jpn J Cancer Res (1997)

PITHD1 is a proteasome-interacting protein essential for male fertilization

por Kondo, Hiroyuki, Matsumura, Takafumi, Kaneko, Mari, Inoue, Kenichi, Kosako, Hidetaka, Ikawa, Masahito, Takahama, Yousuke, Ohigashi, Izumi
Publicado en J Biol Chem (2020)

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

por Kondo, Hiroyuki, Matsushita, Itsuka, Nagata, Tatsuo, Fujihara, Etsuko, Hosono, Katsuhiro, Uchio, Eiichi, Hotta, Yoshihiro, Kusaka, Shunji
Publicado en Transl Vis Sci Technol (2021)

Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome

por Kondo, Hiroyuki, Matsushita, Itsuka, Nagata, Tatsuo, Hayashi, Takaaki, Kakinoki, Masashi, Uchio, Eiichi, Kondo, Mineo, Ohji, Masahito, Kusaka, Shunji
Publicado en Hum Genome Var (2016)

Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study

por Oshima, Yuji, Ishibashi, Yumi, Umeda, Naoyasu, Nagata, Tatsuo, Yoshida, Shigeo, Uchio, Eiichi, Kondo, Hiroyuki, Sonoda, Koh-hei, Ishibashi, Tatsuro
Publicado en BMC Ophthalmol (2021)

Essential role of CCL21 in establishment of central self-tolerance in T cells

por Kozai, Mina, Kubo, Yuki, Katakai, Tomoya, Kondo, Hiroyuki, Kiyonari, Hiroshi, Schaeuble, Karin, Luther, Sanjiv A., Ishimaru, Naozumi, Ohigashi, Izumi, Takahama, Yousuke
Publicado en J Exp Med (2017)

ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME

por Fujimoto, Kazushi, Nagata, Tatsuo, Matsushita, Itsuka, Oku, Kazuma, Imagawa, Mamika, Kuniyoshi, Kazuki, Hayashi, Takaaki, Kimoto, Kenichi, Ohji, Masahito, Kusaka, Shunji, Kondo, Hiroyuki
Publicado en Retina (2021)

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN

por Mizobuchi, Kei, Hayashi, Takaaki, Oishi, Noriko, Kubota, Daiki, Kameya, Shuhei, Higasa, Koichiro, Futami, Takuma, Kondo, Hiroyuki, Hosono, Katsuhiro, Kurata, Kentaro, Hotta, Yoshihiro, Yoshitake, Kazutoshi, Iwata, Takeshi, Matsuura, Tomokazu, Nakano, Tadashi
Publicado en J Clin Med (2021)

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

por Hosono, Katsuhiro, Nishina, Sachiko, Yokoi, Tadashi, Katagiri, Satoshi, Saitsu, Hirotomo, Kurata, Kentaro, Miyamichi, Daisuke, Hikoya, Akiko, Mizobuchi, Kei, Nakano, Tadashi, Minoshima, Shinsei, Fukami, Maki, Kondo, Hiroyuki, Sato, Miho, Hayashi, Takaaki, Azuma, Noriyuki, Hotta, Yoshihiro
Publicado en Sci Rep (2018)

Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy

por Katagiri, Satoshi, Iwasa, Maki, Hayashi, Takaaki, Hosono, Katsuhiro, Yamashita, Takahiro, Kuniyoshi, Kazuki, Ueno, Shinji, Kondo, Mineo, Ueyama, Hisao, Ogita, Hisakazu, Shichida, Yoshinori, Inagaki, Hidehito, Kurahashi, Hiroki, Kondo, Hiroyuki, Ohji, Masahito, Hotta, Yoshihiro, Nakano, Tadashi
Publicado en Sci Rep (2018)

Trans-omics Impact of Thymoproteasome in Cortical Thymic Epithelial Cells

por Ohigashi, Izumi, Tanaka, Yu, Kondo, Kenta, Fujimori, Sayumi, Kondo, Hiroyuki, Palin, Amy C., Hoffmann, Victoria, Kozai, Mina, Matsushita, Yosuke, Uda, Shinsuke, Motosugi, Ryo, Hamazaki, Jun, Kubota, Hiroyuki, Murata, Shigeo, Tanaka, Keiji, Katagiri, Toyomasa, Kosako, Hidetaka, Takahama, Yousuke
Publicado en Cell Rep (2019)