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Investigative Ophthalmology & Visual Science
|
June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night Blindness
Rola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, 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.
Plos One
|
March 30, 2017
Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease
Stanley Lambertus, Nathalie M Bax, Ana Fakin, 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.
Progress in Retinal and Eye Research
|
August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies
Samantha R De Silva, Gavin Arno, Anthony G Robson, et al.
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.
Investigative Ophthalmology & Visual Science
|
August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?
Isabelle Audo, Olivier M Vanakker, Alaric Smith, 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.
Ophthalmology
|
April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular Phenotype
Arundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Human Mutation
|
January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy
Alice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
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of 38
Search research articles
Search
Showing results (191-200 of 372) with videos related to
Sort By:
Page
of 38
Investigative Ophthalmology & Visual Science
|
June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night Blindness
Rola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, 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.
Plos One
|
March 30, 2017
Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease
Stanley Lambertus, Nathalie M Bax, Ana Fakin, 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.
Progress in Retinal and Eye Research
|
August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies
Samantha R De Silva, Gavin Arno, Anthony G Robson, et al.
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.
Investigative Ophthalmology & Visual Science
|
August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?
Isabelle Audo, Olivier M Vanakker, Alaric Smith, 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.
Ophthalmology
|
April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular Phenotype
Arundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Human Mutation
|
January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy
Alice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Page
of 38