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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: kusuhara s. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
A case of POEMS syndrome with cystoid macular edema.
Imai H, Kusuhara S, Nakanishi Y, Teraoka Escaño MF, Yamamoto H, Tsukahara Y, Negi A. Imai H, et al. Among authors: kusuhara s. Am J Ophthalmol. 2005 Mar;139(3):563-6. doi: 10.1016/j.ajo.2004.09.016. Am J Ophthalmol. 2005. PMID: 15767082
Retinal nerve fiber layer thickness in optic tract syndrome.
Tatsumi Y, Kanamori A, Kusuhara A, Nakanishi Y, Kusuhara S, Nakamura M. Tatsumi Y, et al. Among authors: kusuhara a, kusuhara s. Jpn J Ophthalmol. 2005 Jul-Aug;49(4):294-6. doi: 10.1007/s10384-005-0195-y. Jpn J Ophthalmol. 2005. PMID: 16075328
A case of probable Vogt-Koyanagi-Harada disease in a 3-year-old girl.
Katsuyama A, Kusuhara S, Awano H, Nagase H, Matsumiya W, Nakamura M. Katsuyama A, et al. Among authors: kusuhara s. BMC Ophthalmol. 2019 Aug 13;19(1):179. doi: 10.1186/s12886-019-1192-0. BMC Ophthalmol. 2019. PMID: 31409322 Free PMC article.
192 results