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Japanese Journal of Ophthalmology|September 6, 2008
A novel mutation (967-970+2)delAAAGGT in the choroideremia gene found in a Japanese family and related clinical findingsYutaka Iino, Takuro Fujimaki, Keiko Fujiki, et al.Japanese Journal of Ophthalmology|August 6, 2004
Mutations in the membrane component, chromosome 1, surface marker 1 (M1S1) gene in gelatinous drop-like corneal dystrophyAkira Murakami, Shunsuke Kimura, Keiko Fujiki, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|September 12, 2007
In vivo laser confocal microscopic findings of corneal stromal dystrophiesAkira Kobayashi, Keiko Fujiki, Takuro Fujimaki, et al.Japanese Journal of Ophthalmology|November 2, 2011
OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophyTetsuya Hamahata, Takuro Fujimaki, Keiko Fujiki, et al.Japanese Journal of Ophthalmology|July 29, 2008
A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophyTakahiko Seto, Keiko Fujiki, Hitoshi Kishishita, et al.Japanese Journal of Ophthalmology|April 11, 2006
Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucomaYoko Inagaki, Yukihiko Mashima, Nobuo Fuse, et al.Japanese Journal of Ophthalmology|October 23, 2009
A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutationMomoko Himi, Takuro Fujimaki, Toshiyuki Yokoyama, et al.Ophthalmic Genetics|December 23, 2010
A novel nonsense mutation in rhodopsin gene in two Indonesian families with autosomal recessive retinitis pigmentosaArief Kartasasmita, Keiko Fujiki, Erwin Iskandar, et al.Ocular Immunology and Inflammation|May 5, 2009
Bilateral anterior granulomatous keratouveitis with sunset glow fundus in a patient with autoimmune polyglandular syndromeYuri Futagami, Sunao Sugita, Takuro Fujimaki, et al.Journal of Pediatric Ophthalmology and Strabismus|June 10, 2006
Central retinal vein occlusion caused by human herpesvirus 6Yoko Takizawa, Seiichiro Hayashi, Takuro Fujimaki, et al.Pageof 3