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Kaoru Fujinami

Showing results (61-70 of 148) with videos related to

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Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
Investigative Ophthalmology & Visual Science|September 2, 2016
Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4Ana Fakin, Anthony G Robson, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science|November 8, 2016
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous PatientsAna Fakin, Anthony G Robson, John Pei-Wen Chiang, et al.
Medicine|December 23, 2022
A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case reportKeitaro Mizumoto, Kumiko Kato, Kaoru Fujinami, et al.
Japanese Journal of Ophthalmology|March 28, 2026
Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatusTakuhiro Hayakawa, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 27, 2020
Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1Xiao Liu, Xiaohong Meng, Lizhu Yang, et al.
The British Journal of Ophthalmology|November 8, 2023
Stargardt macular dystrophy and therapeutic approachesKaoru Fujinami, Nadia Waheed, Yannik Laich, et al.
Ophthalmic Genetics|December 9, 2017
Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variantsAzusa Kominami, Shinji Ueno, Taro Kominami, et al.
American Journal of Ophthalmology|March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural HistorySagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Journal of Ophthalmology|May 17, 2019
Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning TechniquesYu Fujinami-Yokokawa, Nikolas Pontikos, Lizhu Yang, et al.
Pageof 15

Showing results (61-70 of 148) with videos related to

Sort By:
Pageof 15
Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
Investigative Ophthalmology & Visual Science|September 2, 2016
Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4Ana Fakin, Anthony G Robson, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science|November 8, 2016
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous PatientsAna Fakin, Anthony G Robson, John Pei-Wen Chiang, et al.
Medicine|December 23, 2022
A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case reportKeitaro Mizumoto, Kumiko Kato, Kaoru Fujinami, et al.
Japanese Journal of Ophthalmology|March 28, 2026
Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatusTakuhiro Hayakawa, Kei Mizobuchi, Takaaki Hayashi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 27, 2020
Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1Xiao Liu, Xiaohong Meng, Lizhu Yang, et al.
The British Journal of Ophthalmology|November 8, 2023
Stargardt macular dystrophy and therapeutic approachesKaoru Fujinami, Nadia Waheed, Yannik Laich, et al.
Ophthalmic Genetics|December 9, 2017
Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variantsAzusa Kominami, Shinji Ueno, Taro Kominami, et al.
American Journal of Ophthalmology|March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural HistorySagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Journal of Ophthalmology|May 17, 2019
Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning TechniquesYu Fujinami-Yokokawa, Nikolas Pontikos, Lizhu Yang, et al.
Pageof 15