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Clinical & Experimental Ophthalmology|January 5, 2008
Woman with atypical unilateral Leber's hereditary optic neuropathy with visual improvementEiko Sugisaka, Hisao Ohde, Kei Shinoda, et al.
Japanese Journal of Ophthalmology|January 25, 2003
Macular nerve fibers temporal to fovea may have a greater potential to recover function in patients with Leber's hereditary optic neuropathyYukihiko Mashima, Enrique Adan Sato, Hisao Ohde, et al.
Japanese Journal of Ophthalmology|April 20, 2005
Genetic variants of TP53 and EPHX1 in Leber's hereditary optic neuropathy and their relationship to age at onsetKarin Ishikawa, Tomoyo Funayama, Hisao Ohde, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 23, 2013
Improvement of visual acuity after transcorneal electrical stimulation in case of Best vitelliform macular dystrophyNaoki Ozeki, Kei Shinoda, Hisao Ohde, et al.
Japanese Journal of Ophthalmology|April 6, 2004
Multifocal magnetoencephalogram applied to objective visual field analysisTakatsune Nishiyama, Hisao Ohde, Yasuhiro Haruta, et al.
Clinical & Experimental Ophthalmology|July 29, 2006
Microcirculation at optic disc rim is correlated with visual field defects in cases of anterior ischaemic optic neuropathyShinsuke Yokoyama, Itaru Kimura, Hisao Ohde, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 4, 2006
Phototoxic effects of commercial photographic flash lamp on rat eyesMakoto Inoue, Kei Shinoda, Hisao Ohde, et al.
Frontiers in Human Neuroscience|August 6, 2013
Early Visual Processing is Affected by Clinical Subtype in Patients with Unilateral Spatial Neglect: A Magnetoencephalography StudyKatsuhiro Mizuno, Tetsuya Tsuji, Yves Rossetti, et al.
Clinical Ophthalmology (Auckland, N.Z.)|December 31, 2010
Pattern-reversal visual-evoked potential in patients with occult macular dystrophyGen Hanazono, Hisao Ohde, Kei Shinoda, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 27, 2004
Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisisKei Shinoda, Hisao Ohde, Susumu Ishida, et al.
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