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Kaoru Fujinami

Showing results (31-40 of 148) with videos related to

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Acta Ophthalmologica|February 19, 2010
Stargardt disease with preserved central vision: identification of a putative novel mutation in ATP-binding cassette transporter geneKaoru Fujinami, Masakazu Akahori, Masaki Fukui, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 24, 2018
ISCEV extended protocol for the dark-adapted red flash ERGDorothy A Thompson, Kaoru Fujinami, Ido Perlman, et al.
Retina (Philadelphia, Pa.)|August 16, 2021
RETINAL SURFACE WRINKLING AS AN INDICATOR FOR INTERNAL LIMITING MEMBRANE PEELING DURING VITRECTOMY FOR RETINAL DETACHMENTKunihiko Akiyama, Kaoru Fujinami, Ken Watanabe, et al.
Retina (Philadelphia, Pa.)|November 10, 2023
PREVALENCE AND CLINICAL FEATURES OF RADIAL FUNDUS AUTOFLUORESCENCE IN HIGH MYOPIC WOMENShih-Wen Wang, Tae Igarashi-Yokoi, Shiho Mochida, et al.
The British Journal of Ophthalmology|November 21, 2007
Transient macular dysfunction determined by focal macular electroretinogramNaoki Terauchi, Kaoru Fujinami, Kei Shinoda, et al.
Ophthalmic Genetics|June 23, 2022
A recurrent variant in <i>LIM2</i> causes an isolated congenital sutural/lamellar cataract in a Japanese familyVanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki, et al.
Acta Ophthalmologica|September 12, 2013
Fine central macular dots associated with childhood-onset Stargardt DiseaseKaoru Fujinami, Ravjit Singh, Joseph Carroll, et al.
Plos One|November 3, 2017
Advanced quantitative analysis of the sub-retinal pigment epithelial space in recurrent neovascular age-related macular degenerationMariko Sasaki, Yu Kato, Kaoru Fujinami, et al.
American Journal of Medical Genetics. Part A|June 18, 2025
A de novo HK1 Variant in a Boy Fulfilling the Diagnostic Criteria for Tuberous Sclerosis Complex: Expanding the Phenotypic Spectrum of NEDVIBADaisuke Ariyasu, Hiroaki Sato, Hideo Cho, et al.
Investigative Ophthalmology & Visual Science|December 3, 2017
Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular DystrophyYu Kato, Gen Hanazono, Kaoru Fujinami, et al.
Pageof 15

Showing results (31-40 of 148) with videos related to

Sort By:
Pageof 15
Acta Ophthalmologica|February 19, 2010
Stargardt disease with preserved central vision: identification of a putative novel mutation in ATP-binding cassette transporter geneKaoru Fujinami, Masakazu Akahori, Masaki Fukui, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 24, 2018
ISCEV extended protocol for the dark-adapted red flash ERGDorothy A Thompson, Kaoru Fujinami, Ido Perlman, et al.
Retina (Philadelphia, Pa.)|August 16, 2021
RETINAL SURFACE WRINKLING AS AN INDICATOR FOR INTERNAL LIMITING MEMBRANE PEELING DURING VITRECTOMY FOR RETINAL DETACHMENTKunihiko Akiyama, Kaoru Fujinami, Ken Watanabe, et al.
Retina (Philadelphia, Pa.)|November 10, 2023
PREVALENCE AND CLINICAL FEATURES OF RADIAL FUNDUS AUTOFLUORESCENCE IN HIGH MYOPIC WOMENShih-Wen Wang, Tae Igarashi-Yokoi, Shiho Mochida, et al.
The British Journal of Ophthalmology|November 21, 2007
Transient macular dysfunction determined by focal macular electroretinogramNaoki Terauchi, Kaoru Fujinami, Kei Shinoda, et al.
Ophthalmic Genetics|June 23, 2022
A recurrent variant in <i>LIM2</i> causes an isolated congenital sutural/lamellar cataract in a Japanese familyVanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki, et al.
Acta Ophthalmologica|September 12, 2013
Fine central macular dots associated with childhood-onset Stargardt DiseaseKaoru Fujinami, Ravjit Singh, Joseph Carroll, et al.
Plos One|November 3, 2017
Advanced quantitative analysis of the sub-retinal pigment epithelial space in recurrent neovascular age-related macular degenerationMariko Sasaki, Yu Kato, Kaoru Fujinami, et al.
American Journal of Medical Genetics. Part A|June 18, 2025
A de novo HK1 Variant in a Boy Fulfilling the Diagnostic Criteria for Tuberous Sclerosis Complex: Expanding the Phenotypic Spectrum of NEDVIBADaisuke Ariyasu, Hiroaki Sato, Hideo Cho, et al.
Investigative Ophthalmology & Visual Science|December 3, 2017
Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular DystrophyYu Kato, Gen Hanazono, Kaoru Fujinami, et al.
Pageof 15