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Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, Terasaki H, Kominami T, Nao-I N, Mawatari G, Mizota A, Shinoda K, Kondo M, Kato K, Sekiryu T, Nakamura M, Kusuhara S, Yamamoto H, Yamamoto S, Mochizuki K, Kondo H, Matsushita I, Kameya S, Fukuchi T, Hatase T, Horiguchi M, Shimada Y, Tanikawa A, Yamamoto S, Miura G, Ito N, Murakami A, Fujimaki T, Hotta Y, Tanaka K, Iwata T. Suga A, et al. Among authors: horiguchi m. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
Fundus albipunctatus associated with cone dystrophy.
Miyake Y, Shiroyama N, Sugita S, Horiguchi M, Yagasaki K. Miyake Y, et al. Among authors: horiguchi m. Br J Ophthalmol. 1992 Jun;76(6):375-9. doi: 10.1136/bjo.76.6.375. Br J Ophthalmol. 1992. PMID: 1622952 Free PMC article.
Light deprivation and retinitis pigmentosa.
Miyake Y, Sugita S, Horiguchi M, Yagasaki K. Miyake Y, et al. Among authors: horiguchi m. Am J Ophthalmol. 1990 Sep 15;110(3):305-6. doi: 10.1016/s0002-9394(14)76350-0. Am J Ophthalmol. 1990. PMID: 2396657 No abstract available.
Asymmetry of focal ERG in human macular region.
Miyake Y, Shiroyama N, Horiguchi M, Ota I. Miyake Y, et al. Among authors: horiguchi m. Invest Ophthalmol Vis Sci. 1989 Aug;30(8):1743-9. Invest Ophthalmol Vis Sci. 1989. PMID: 2759790
495 results