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Ophthalmology|October 31, 2006
A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responsesTakaaki Hayashi, Tamaki Gekka, Tomokazu Takeuchi, et al.Ophthalmic Surgery, Lasers & Imaging Retina|April 19, 2019
Long-Term Course Following Vitreous Surgery for Epiretinal MembraneTakefumi Kishi, Akira Watanabe, Shoyo Yoshimine, et al.Journal of Cataract and Refractive Surgery|December 26, 2015
Trisection technique for the extraction of dislocated intraocular lenses through a small surgical incisionTamaki Gekka, Tomoichiro Ogawa, Yasuhiro Ohkuma, et al.Documenta Ophthalmologica. Advances in Ophthalmology|March 10, 2012
Improvement of central visual function following steroid pulse therapy in acute zonal occult outer retinopathyTakaaki Kitakawa, Takaaki Hayashi, Hirotsugu Takashina, et al.Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|September 2, 2015
Efficacy of Intravitreal Triamcinolone Acetonide for Diabetic Macular Edema After VitrectomyAkira Watanabe, Akane Tsuzuki, Kota Arai, et al.Optometry and Vision Science : Official Publication of the American Academy of Optometry|August 11, 2015
Improved Photoreceptor Function in Male Acute Zonal Occult Outer RetinopathyTsutomu Sakai, Tamaki Gekka, Kenichi Kohzaki, et al.Acta Ophthalmologica Scandinavica|April 28, 2006
Compound heterozygous RDH5 mutations in familial fleck retina with night blindnessTakaaki Hayashi, Satoshi Goto-Omoto, Tomokazu Takeuchi, et al.Visual Neuroscience|September 12, 2006
Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsiaSatoshi Goto-Omoto, Takaaki Hayashi, Tamaki Gekka, et al.Ophthalmology|October 18, 2005
Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosityTakaaki Hayashi, Tamaki Gekka, Satoshi Goto-Omoto, et al.Visual Neuroscience|September 12, 2006
Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defectTakaaki Hayashi, Akiko Kubo, Tomokazu Takeuchi, et al.Pageof 4