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Page 1
Survey of microphthalmia in Japan.
Nishina S, Kurosaka D, Nishida Y, Kondo H, Kobayashi Y, Azuma N. Nishina S, et al. Among authors: kondo h. Jpn J Ophthalmol. 2012 May;56(3):198-202. doi: 10.1007/s10384-012-0126-7. Epub 2012 Feb 23. Jpn J Ophthalmol. 2012. PMID: 22358587
Foveal Hypoplasia in Patients with Stickler Syndrome.
Matsushita I, Nagata T, Hayashi T, Kimoto K, Kubota T, Ohji M, Kusaka S, Kondo H. Matsushita I, et al. Among authors: kondo h. Ophthalmology. 2017 Jun;124(6):896-902. doi: 10.1016/j.ophtha.2017.01.046. Epub 2017 Mar 7. Ophthalmology. 2017. PMID: 28283280
Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.
Katagiri S, Iwasa M, Hayashi T, Hosono K, Yamashita T, Kuniyoshi K, Ueno S, Kondo M, Ueyama H, Ogita H, Shichida Y, Inagaki H, Kurahashi H, Kondo H, Ohji M, Hotta Y, Nakano T. Katagiri S, et al. Among authors: kondo m, kondo h. Sci Rep. 2018 Jul 31;8(1):11507. doi: 10.1038/s41598-018-29891-9. Sci Rep. 2018. PMID: 30065301 Free PMC article.
Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.
Kondo H, Oku K, Katagiri S, Hayashi T, Nakano T, Iwata A, Kuniyoshi K, Kusaka S, Hiyoshi A, Uchio E, Kondo M, Oishi N, Kameya S, Mizota A, Naoi N, Ueno S, Terasaki H, Morimoto T, Iwaki M, Yoshitake K, Iejima D, Fujinami K, Tsunoda K, Shinoda K, Iwata T. Kondo H, et al. Among authors: kondo m. Hum Genome Var. 2019 Jan 8;6:3. doi: 10.1038/s41439-018-0034-6. eCollection 2019. Hum Genome Var. 2019. PMID: 30652005 Free PMC article.
Electroretinograms of eyes with Stickler syndrome.
Kondo H, Fujimoto K, Imagawa M, Oku K, Matsushita I, Hayashi T, Nagata T. Kondo H, et al. Doc Ophthalmol. 2020 Jun;140(3):233-243. doi: 10.1007/s10633-019-09739-x. Epub 2019 Nov 28. Doc Ophthalmol. 2020. PMID: 31781920
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency.
Yang L, Fujinami K, Ueno S, Kuniyoshi K, Hayashi T, Kondo M, Mizota A, Naoi N, Shinoda K, Kameya S, Fujinami-Yokokawa Y, Liu X, Arno G, Pontikos N, Kominami T, Terasaki H, Sakuramoto H, Katagiri S, Mizobuchi K, Nakamura N, Mawatari G, Kurihara T, Tsubota K, Miyake Y, Yoshitake K, Iwata T, Tsunoda K; JEGC study group. Yang L, et al. Among authors: kondo m. Sci Rep. 2020 Mar 26;10(1):5497. doi: 10.1038/s41598-020-62119-3. Sci Rep. 2020. PMID: 32218477 Free PMC article.
RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort.
Katagiri S, Hayashi T, Nakamura M, Mizobuchi K, Gekka T, Komori S, Ueno S, Terasaki H, Sakuramoto H, Kuniyoshi K, Kusaka S, Nagashima R, Kondo M, Fujinami K, Tsunoda K, Matsuura T, Kondo H, Yoshitake K, Iwata T, Nakano T. Katagiri S, et al. Among authors: kondo m, kondo h. Invest Ophthalmol Vis Sci. 2020 Mar 9;61(3):53. doi: 10.1167/iovs.61.3.53. Invest Ophthalmol Vis Sci. 2020. PMID: 32232344 Free PMC article.
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.
Fujinami-Yokokawa Y, Fujinami K, Kuniyoshi K, Hayashi T, Ueno S, Mizota A, Shinoda K, Arno G, Pontikos N, Yang L, Liu X, Sakuramoto H, Katagiri S, Mizobuchi K, Kominami T, Terasaki H, Nakamura N, Kameya S, Yoshitake K, Miyake Y, Kurihara T, Tsubota K, Miyata H, Iwata T, Tsunoda K; Japan Eye Genetics Consortium. Fujinami-Yokokawa Y, et al. Sci Rep. 2020 Jun 12;10(1):9531. doi: 10.1038/s41598-020-65737-z. Sci Rep. 2020. PMID: 32533067 Free PMC article.
3,757 results