Kenichi Kozaki

Clinical heterogeneity between two Japanese siblings with congenital achromatopsia

Takaaki Hayashi, Kenichi Kozaki, K. Kitahara, 2004, Visual Neuroscience.

Subfoveal choroidal thickness in multiple evanescent white dot syndrome

Takaaki Hayashi, Kenichi Kozaki, H. Tsuneoka, 2012, Clinical & experimental optometry.

Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.

Takaaki Hayashi, Kenichi Kozaki, K. Kitahara, 2004, American journal of ophthalmology.

Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene

M. Urashima, Takaaki Hayashi, Kenichi Kozaki, 2011, Ophthalmic Research.

Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).

Takaaki Hayashi, Kenichi Kozaki, K. Kitahara, 2004, Acta ophthalmologica Scandinavica.

Multifocal electroretinographic evaluation of macular function in acute posterior multifocal placoid pigment epitheliopathy

Takaaki Hayashi, Kenichi Kozaki, H. Tsuneoka, 2013, Documenta Ophthalmologica.

Improvement of visual function in bilateral acute zonal occult outer retinopathy

M. Kinoshita, Takaaki Hayashi, Kenichi Kozaki, 2012 .

Autosomal Dominant Occult Macular Dystrophy with an RP1L1 Mutation (R45W)

Hisashi Yamada, Takaaki Hayashi, Kenichi Kozaki, 2012, Optometry and vision science : official publication of the American Academy of Optometry.

Change in anterior chamber depth following combined pars plana vitrectomy, phacoemulsification, and intraocular lens implantation using different types of intraocular lenses

Kenichi Kozaki, Akira Watanabe, H. Tsuneoka, 2010, Japanese Journal of Ophthalmology.