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Kaoru Fujinami

Showing results (101-110 of 148) with videos related to

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Investigative Ophthalmology & Visual Science|May 19, 2026
Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence TomographyHirohiko Kawashima, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Ophthalmology|May 11, 2016
Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy in Japanese CohortAyami Nakanishi, Shinji Ueno, Takaaki Hayashi, et al.
Scientific Reports|November 16, 2019
Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophiesKei Mizobuchi, Takaaki Hayashi, Satoshi Katagiri, et al.
Genes|November 27, 2021
Genetic and Phenotypic Landscape of <i>PRPH2</i>-Associated Retinal Dystrophy in JapanAkio Oishi, Kaoru Fujinami, Go Mawatari, et al.
Genes|October 28, 2023
Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No. 5Yu Fujinami-Yokokawa, Lizhu Yang, Kwangsic Joo, et al.
NPJ Genomic Medicine|April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severityRiccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Human Genome Variation|October 25, 2019
Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
American Journal of Ophthalmology|February 10, 2023
Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17)Rupert W Strauss, Alexander Ho, Anamika Jha, et al.
American Journal of Ophthalmology|August 18, 2025
SNRNP200- associated Retinopathy: In-depth Clinical Phenotyping and Genetic CharacterizationJuan C Romo-Aguas, Yannik Laich, Angelos Kalitzeos, et al.
Human Genome Variation|February 13, 2020
Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Pageof 15

Showing results (101-110 of 148) with videos related to

Sort By:
Pageof 15
Investigative Ophthalmology & Visual Science|May 19, 2026
Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence TomographyHirohiko Kawashima, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Ophthalmology|May 11, 2016
Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy in Japanese CohortAyami Nakanishi, Shinji Ueno, Takaaki Hayashi, et al.
Scientific Reports|November 16, 2019
Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophiesKei Mizobuchi, Takaaki Hayashi, Satoshi Katagiri, et al.
Genes|November 27, 2021
Genetic and Phenotypic Landscape of <i>PRPH2</i>-Associated Retinal Dystrophy in JapanAkio Oishi, Kaoru Fujinami, Go Mawatari, et al.
Genes|October 28, 2023
Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No. 5Yu Fujinami-Yokokawa, Lizhu Yang, Kwangsic Joo, et al.
NPJ Genomic Medicine|April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severityRiccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Human Genome Variation|October 25, 2019
Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
American Journal of Ophthalmology|February 10, 2023
Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17)Rupert W Strauss, Alexander Ho, Anamika Jha, et al.
American Journal of Ophthalmology|August 18, 2025
SNRNP200- associated Retinopathy: In-depth Clinical Phenotyping and Genetic CharacterizationJuan C Romo-Aguas, Yannik Laich, Angelos Kalitzeos, et al.
Human Genome Variation|February 13, 2020
Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-associated retinal disorder: report of eight novel variantsGo Mawatari, Kaoru Fujinami, Xiao Liu, et al.
Pageof 15