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American Journal of Ophthalmology
|
August 20, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function
Kaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
JMIR Medical Informatics
|
December 13, 2021
Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review
Howard Maile, Ji-Peng Olivia Li, Daniel Gore, et al.
Ophthalmology Science
|
April 23, 2026
Genetic and Phenotypic Characterization of a Large Cohort of Patients with BBS1-Retinopathy
Juan C Romo-Aguas, Thales A C de Guimarāes, Angelos Kalitzeos, et al.
American Journal of Ophthalmology
|
March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations
Kaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
American Journal of Ophthalmology
|
October 8, 2023
RBP3-Retinopathy-Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping
Michalis Georgiou, Kaoru Fujinami, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science
|
January 7, 2022
Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3
Seong Joon Ahn, Lizhu Yang, Kazushige Tsunoda, et al.
American Journal of Ophthalmology
|
May 5, 2021
The Progression of Stargardt Disease Using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15
Etienne M Schönbach, Lucas Janeschitz-Kriegl, Rupert W Strauss, et al.
Investigative Ophthalmology & Visual Science
|
April 2, 2020
RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort
Satoshi Katagiri, Takaaki Hayashi, Masaki Nakamura, et al.
Ophthalmology
|
April 28, 2019
Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1
Kaoru Fujinami, Lizhu Yang, Kwangsic Joo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 22, 2020
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population
Kaoru Fujinami, Akio Oishi, Lizhu Yang, et al.
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of 15
Search research articles
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Showing results (111-120 of 148) with videos related to
Sort By:
Page
of 15
American Journal of Ophthalmology
|
August 20, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function
Kaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
JMIR Medical Informatics
|
December 13, 2021
Machine Learning Algorithms to Detect Subclinical Keratoconus: Systematic Review
Howard Maile, Ji-Peng Olivia Li, Daniel Gore, et al.
Ophthalmology Science
|
April 23, 2026
Genetic and Phenotypic Characterization of a Large Cohort of Patients with BBS1-Retinopathy
Juan C Romo-Aguas, Thales A C de Guimarāes, Angelos Kalitzeos, et al.
American Journal of Ophthalmology
|
March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations
Kaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
American Journal of Ophthalmology
|
October 8, 2023
RBP3-Retinopathy-Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping
Michalis Georgiou, Kaoru Fujinami, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science
|
January 7, 2022
Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3
Seong Joon Ahn, Lizhu Yang, Kazushige Tsunoda, et al.
American Journal of Ophthalmology
|
May 5, 2021
The Progression of Stargardt Disease Using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15
Etienne M Schönbach, Lucas Janeschitz-Kriegl, Rupert W Strauss, et al.
Investigative Ophthalmology & Visual Science
|
April 2, 2020
RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort
Satoshi Katagiri, Takaaki Hayashi, Masaki Nakamura, et al.
Ophthalmology
|
April 28, 2019
Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1
Kaoru Fujinami, Lizhu Yang, Kwangsic Joo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 22, 2020
Clinical and genetic characteristics of 10 Japanese patients with PROM1-associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population
Kaoru Fujinami, Akio Oishi, Lizhu Yang, et al.
Page
of 15