Search research articles
Contact Us
Filters
Showing results (91-100 of 148) with videos related to
Page
of 15
Sort By:
American Journal of Ophthalmology
|
February 16, 2024
Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal Dystrophy
Shaima Awadh Hashem, Michalis Georgiou, Yu Fujinami-Yokokawa, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
February 16, 2019
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia
Kai Suzuki, Kiyoko Gocho, Keiichiro Akeo, et al.
Ophthalmology. Retina
|
September 1, 2024
PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural History
Shaima Awadh Hashem, Michalis Georgiou, Genevieve Wright, et al.
Investigative Ophthalmology & Visual Science
|
November 15, 2019
Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings
Natsuko Nakamura, Kazushige Tsunoda, Yoshinobu Mizuno, et al.
Progress in Retinal and Eye Research
|
January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
JAMA Ophthalmology
|
June 15, 2018
Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10
Xiangrong Kong, Kaoru Fujinami, Rupert W Strauss, et al.
Investigative Ophthalmology & Visual Science
|
April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome
Juan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
American Journal of Ophthalmology
|
July 23, 2021
Longitudinal Changes of Fixation Stability and Location Within 24 Months in Stargardt Disease: ProgStar Report No. 16
Etienne M Schönbach, Rupert W Strauss, Marco E G V Cattaneo, et al.
Ophthalmology. Retina
|
June 18, 2023
CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural History
Malena Daich Varela, Emma S Duignan, Samantha R De Silva, et al.
Ophthalmology Science
|
April 23, 2026
Fundus Autofluorescence as a Sensitive Biomarker of Disease Progression in Bietti Crystalline Dystrophy
Huanyu Zhao, Masatoshi Fukushima, Takahiro Hisai, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 148) with videos related to
Sort By:
Page
of 15
American Journal of Ophthalmology
|
February 16, 2024
Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal Dystrophy
Shaima Awadh Hashem, Michalis Georgiou, Yu Fujinami-Yokokawa, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
February 16, 2019
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia
Kai Suzuki, Kiyoko Gocho, Keiichiro Akeo, et al.
Ophthalmology. Retina
|
September 1, 2024
PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural History
Shaima Awadh Hashem, Michalis Georgiou, Genevieve Wright, et al.
Investigative Ophthalmology & Visual Science
|
November 15, 2019
Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings
Natsuko Nakamura, Kazushige Tsunoda, Yoshinobu Mizuno, et al.
Progress in Retinal and Eye Research
|
January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
JAMA Ophthalmology
|
June 15, 2018
Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10
Xiangrong Kong, Kaoru Fujinami, Rupert W Strauss, et al.
Investigative Ophthalmology & Visual Science
|
April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome
Juan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
American Journal of Ophthalmology
|
July 23, 2021
Longitudinal Changes of Fixation Stability and Location Within 24 Months in Stargardt Disease: ProgStar Report No. 16
Etienne M Schönbach, Rupert W Strauss, Marco E G V Cattaneo, et al.
Ophthalmology. Retina
|
June 18, 2023
CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural History
Malena Daich Varela, Emma S Duignan, Samantha R De Silva, et al.
Ophthalmology Science
|
April 23, 2026
Fundus Autofluorescence as a Sensitive Biomarker of Disease Progression in Bietti Crystalline Dystrophy
Huanyu Zhao, Masatoshi Fukushima, Takahiro Hisai, et al.
Page
of 15