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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.
Frontiers in Neuroscience
|
October 25, 2021
Structural and Functional Characteristics of Color Vision Changes in Choroideremia
Jasleen K Jolly, Matthew P Simunovic, Adam M Dubis, et al.
American Journal of Ophthalmology
|
November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers
Michalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science
|
December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive Inheritance
Neringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
The British Journal of Ophthalmology
|
October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1
Robert H Henderson, Donna S Mackay, Zheng Li, et al.
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.
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.
Investigative Ophthalmology & Visual Science
|
November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk Polymorphism
Zihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica
|
January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case series
Marie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
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of 19
Search research articles
Search
Showing results (121-130 of 188) with videos related to
Sort By:
Page
of 19
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.
Frontiers in Neuroscience
|
October 25, 2021
Structural and Functional Characteristics of Color Vision Changes in Choroideremia
Jasleen K Jolly, Matthew P Simunovic, Adam M Dubis, et al.
American Journal of Ophthalmology
|
November 17, 2023
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers
Michalis Georgiou, Anthony G Robson, Sami H Uwaydat, et al.
Investigative Ophthalmology & Visual Science
|
December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive Inheritance
Neringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
The British Journal of Ophthalmology
|
October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1
Robert H Henderson, Donna S Mackay, Zheng Li, et al.
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.
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.
Investigative Ophthalmology & Visual Science
|
November 12, 2024
The Electroretinogram I-Wave, a Component Originating in the Retinal OFF-Pathway, Associates With a Myopia Genetic Risk Polymorphism
Zihe Xu, Jit Kai Tan, Krishnika Vetrivel, et al.
Acta Ophthalmologica
|
January 1, 2019
Unilateral pigmentary retinopathy: a retrospective case series
Marie-Hélène Errera, Anthony G Robson, Tracey Wong, et al.
Page
of 19