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Kaoru Fujinami

Showing results (41-50 of 148) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|July 11, 2020
Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1)Ayane Hirose, Satoshi Katagiri, Takaaki Hayashi, et al.
Molecular Genetics & Genomic Medicine|May 23, 2020
Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findingsKei Mizobuchi, Takaaki Hayashi, Kazutoshi Yoshitake, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 26, 2020
Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-upXiao Liu, Lixia Gao, Gang Wang, et al.
Translational Vision Science & Technology|March 6, 2019
Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt DiseasePreena Tanna, Michalis Georgiou, Rupert W Strauss, et al.
SAGE Open Medical Case Reports|September 25, 2020
Fish oil supplementation and repeated macular hemorrhage without choroidal neovascularization: A case reportShi-Ying Li, Kaoru Fujinami, Sheila G Crewther, et al.
Japanese Journal of Ophthalmology|January 4, 2019
Three cases of acute-onset bilateral photophobiaShinji Ueno, Daiki Inooka, Monika Meinert, et al.
Japanese Journal of Ophthalmology|November 12, 2020
Acute unilateral inner retinal dysfunction with photophobia: importance of electrodiagnosisToshiaki Hirakata, Kaoru Fujinami, Wataru Saito, et al.
Ophthalmic Genetics|January 14, 2022
Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in <i>NMNAT1</i>: a case report and mini reviewTomoyasu Kayazawa, Kazuki Kuniyoshi, Yoshikazu Hatsukawa, et al.
American Journal of Ophthalmology|August 16, 2020
Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural HistoryMichalis Georgiou, Parampal S Grewal, Akshay Narayan, et al.
Investigative Ophthalmology & Visual Science|July 20, 2018
A Cross-Sectional and Longitudinal Study of Retinal Sensitivity in RPE65-Associated Leber Congenital AmaurosisNeruban Kumaran, Gary S Rubin, Angelos Kalitzeos, et al.
Pageof 15

Showing results (41-50 of 148) with videos related to

Sort By:
Pageof 15
Documenta Ophthalmologica. Advances in Ophthalmology|July 11, 2020
Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1)Ayane Hirose, Satoshi Katagiri, Takaaki Hayashi, et al.
Molecular Genetics & Genomic Medicine|May 23, 2020
Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findingsKei Mizobuchi, Takaaki Hayashi, Kazutoshi Yoshitake, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 26, 2020
Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-upXiao Liu, Lixia Gao, Gang Wang, et al.
Translational Vision Science & Technology|March 6, 2019
Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt DiseasePreena Tanna, Michalis Georgiou, Rupert W Strauss, et al.
SAGE Open Medical Case Reports|September 25, 2020
Fish oil supplementation and repeated macular hemorrhage without choroidal neovascularization: A case reportShi-Ying Li, Kaoru Fujinami, Sheila G Crewther, et al.
Japanese Journal of Ophthalmology|January 4, 2019
Three cases of acute-onset bilateral photophobiaShinji Ueno, Daiki Inooka, Monika Meinert, et al.
Japanese Journal of Ophthalmology|November 12, 2020
Acute unilateral inner retinal dysfunction with photophobia: importance of electrodiagnosisToshiaki Hirakata, Kaoru Fujinami, Wataru Saito, et al.
Ophthalmic Genetics|January 14, 2022
Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in <i>NMNAT1</i>: a case report and mini reviewTomoyasu Kayazawa, Kazuki Kuniyoshi, Yoshikazu Hatsukawa, et al.
American Journal of Ophthalmology|August 16, 2020
Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural HistoryMichalis Georgiou, Parampal S Grewal, Akshay Narayan, et al.
Investigative Ophthalmology & Visual Science|July 20, 2018
A Cross-Sectional and Longitudinal Study of Retinal Sensitivity in RPE65-Associated Leber Congenital AmaurosisNeruban Kumaran, Gary S Rubin, Angelos Kalitzeos, et al.
Pageof 15