Showing results (41-50 of 117) with videos related to
Sort By:
Pageof 12
Translational Vision Science & Technology|June 15, 2021
Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 GeneHiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, et al.Human Genome Variation|November 1, 2019
Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutationsDaisuke Miyamichi, Sachiko Nishina, Katsuhiro Hosono, et al.Japanese Journal of Ophthalmology|April 19, 2018
Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutationsKentaro Kurata, Katsuhiro Hosono, Akiko Hikoya, et al.Retina (Philadelphia, Pa.)|August 12, 2017
ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISK REGIONTadashi Yokoi, Satoshi Katagiri, Miina Hiraoka, et al.Ophthalmology|March 4, 2006
Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophyMakoto Nakamura, Jian Lin, Shinji Ueno, et al.European Journal of Pharmacology|July 29, 2008
Mouse strain differences in immobility and sensitivity to fluvoxamine and desipramine in the forced swimming test: analysis of serotonin and noradrenaline transporter bindingYumi Sugimoto, Yoshinobu Kajiwara, Kazufumi Hirano, et al.Journal of Human Genetics|May 20, 2011
Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populationsHiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.Human Genome Variation|April 18, 2019
A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variantsMuhammad Nazmul Haque, Kentaro Kurata, Katsuhiro Hosono, et al.Journal of Human Genetics|September 17, 2010
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1Hiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.Human Genome Variation|June 9, 2016
Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacyChunxia Wang, Katsuhiro Hosono, Shu Kachi, et al.Pageof 12