Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Taiga Inooka

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 13, 2026
Petrolatum-based ointment application induces swelling of the PRESERFLO MicroshuntRyo Tomita, Taiga Inooka, Takato Kajita, et al.
Ophthalmology Science|February 18, 2026
Association of High-Density Lipoprotein Cholesterol with Macular Structure in Nonglaucomatous IndividualsTaiga Inooka, Ryo Tomita, Ayana Suzumura, et al.
Plos One|April 24, 2023
Assessment of factors affecting flicker ERGs recorded with RETeval from data obtained from health checkup screeningTaiga Inooka, Taro Kominami, Shunsuke Yasuda, et al.
Scientific Reports|December 5, 2024
Assessment of factors affecting anterior chamber depth from data obtained from health checkup participants in JapanTaiga Inooka, Taro Kominami, Ryo Tomita, et al.
Scientific Reports|October 28, 2024
Phenotypic variability of RP1-related inherited retinal dystrophy associated with the c.5797 C > T (p.Arg1933*) variant in the Japanese populationKeigo Natsume, Taro Kominami, Kensuke Goto, et al.
Genetics in Medicine Open|December 13, 2024
A homozygous structural variant of <i>RPGRIP1</i> is frequently associated with achromatopsia in Japanese patients with IRDAkiko Suga, Kei Mizobuchi, Taiga Inooka, et al.
Ophthalmology Science|February 23, 2026
Evolving Consultation: Enhancing Ophthalmic Diagnostic Performance Using Large Language ModelTaiga Inooka, Hikaru Ota, Yosuke Taki, et al.
Retina (Philadelphia, Pa.)|September 17, 2024
GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPANTaiga Inooka, Takaaki Hayashi, Kazushige Tsunoda, et al.
Retina (Philadelphia, Pa.)|February 10, 2026
Deletion involving exon 18 of RPGRIP1 is a major cause of achromatopsiaTaiga Inooka, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Ophthalmology|May 8, 2026
Genotype-phenotype correlations in RPGRIP1-associated retinal dystrophy in a nationwide Japanese cohortKei Mizobuchi, Taiga Inooka, Takuya Aoki, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 13, 2026
Petrolatum-based ointment application induces swelling of the PRESERFLO MicroshuntRyo Tomita, Taiga Inooka, Takato Kajita, et al.
Ophthalmology Science|February 18, 2026
Association of High-Density Lipoprotein Cholesterol with Macular Structure in Nonglaucomatous IndividualsTaiga Inooka, Ryo Tomita, Ayana Suzumura, et al.
Plos One|April 24, 2023
Assessment of factors affecting flicker ERGs recorded with RETeval from data obtained from health checkup screeningTaiga Inooka, Taro Kominami, Shunsuke Yasuda, et al.
Scientific Reports|December 5, 2024
Assessment of factors affecting anterior chamber depth from data obtained from health checkup participants in JapanTaiga Inooka, Taro Kominami, Ryo Tomita, et al.
Scientific Reports|October 28, 2024
Phenotypic variability of RP1-related inherited retinal dystrophy associated with the c.5797 C > T (p.Arg1933*) variant in the Japanese populationKeigo Natsume, Taro Kominami, Kensuke Goto, et al.
Genetics in Medicine Open|December 13, 2024
A homozygous structural variant of <i>RPGRIP1</i> is frequently associated with achromatopsia in Japanese patients with IRDAkiko Suga, Kei Mizobuchi, Taiga Inooka, et al.
Ophthalmology Science|February 23, 2026
Evolving Consultation: Enhancing Ophthalmic Diagnostic Performance Using Large Language ModelTaiga Inooka, Hikaru Ota, Yosuke Taki, et al.
Retina (Philadelphia, Pa.)|September 17, 2024
GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPANTaiga Inooka, Takaaki Hayashi, Kazushige Tsunoda, et al.
Retina (Philadelphia, Pa.)|February 10, 2026
Deletion involving exon 18 of RPGRIP1 is a major cause of achromatopsiaTaiga Inooka, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Ophthalmology|May 8, 2026
Genotype-phenotype correlations in RPGRIP1-associated retinal dystrophy in a nationwide Japanese cohortKei Mizobuchi, Taiga Inooka, Takuya Aoki, et al.
Pageof 2