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Japanese Journal of Ophthalmology|January 4, 2019
Three cases of acute-onset bilateral photophobiaShinji Ueno, Daiki Inooka, Monika Meinert, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 27, 2007
Transcorneal electrical stimulation of retina to treat longstanding retinal artery occlusionKoichi Inomata, Kei Shinoda, Hisao Ohde, et al.Retina (Philadelphia, Pa.)|April 3, 2012
Clinical characteristics of occult macular dystrophy in family with mutation of RP1l1 geneKazushige Tsunoda, Tomoaki Usui, Tetsuhisa Hatase, et al.Case Reports in Ophthalmology|January 1, 2013
Acute Visual Field Defect following Vitrectomy Determined to Originate from Optic Nerve by Electrophysiological TestsAtsuro Uchida, Kei Shinoda, Celso Soiti Matsumoto, et al.American Journal of Human Genetics|September 10, 2010
Dominant mutations in RP1L1 are responsible for occult macular dystrophyMasakazu Akahori, Kazushige Tsunoda, Yozo Miyake, et al.Molecular Vision|November 2, 2019
Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohortAkiko Maeda-Katahira, Natsuko Nakamura, Takaaki Hayashi, et al.Pageof 3