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JAMA Network Open
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June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal Degeneration
Jasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Genes
|
December 16, 2020
Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL
Susan M Downes, Tham Nguyen, Vicky Tai, et al.
Rheumatology Advances in Practice
|
August 22, 2019
An audit of the use of hydroxychloroquine in rheumatology clinics
Claudia Worth, Imran H Yusuf, Bethany Turner, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
July 7, 2023
New Imaging Technology for Simultaneous Multiwavelength-UWF Fundus Fluorescein Angiography and Indocyanine Green Angiography With Navigated Central and Peripheral SS-OCT
Francisco Javier Valentin Bravo, William Ayliffe, Sebastian Francis Eduardo Stanga, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Cells
|
August 26, 2023
The Role of Inflammation in Age-Related Macular Degeneration-Therapeutic Landscapes in Geographic Atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Monica L Hu, et al.
Genes
|
December 30, 2025
Expanding the Genetic Spectrum in <i>IMPG1</i> and <i>IMPG2</i> Retinopathy
Saoud Al-Khuzaei, Ahmed K Shalaby, Jing Yu, et al.
Frontiers in Neuroscience
|
July 16, 2024
Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Benjamin W J Ng, et al.
The British Journal of Ophthalmology
|
July 22, 2017
Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA<sup>Lys</sup> (m.8340G>A) gene variant
Jaidip S Gill, Steven A Hardy, Emma L Blakely, et al.
The British Journal of Ophthalmology
|
June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophies
Ryan Combs, Georgina Hall, Katherine Payne, et al.
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of 14
Search research articles
Search
Showing results (61-70 of 131) with videos related to
Sort By:
Page
of 14
JAMA Network Open
|
June 15, 2019
Clinical and Molecular Characterization of PROM1-Related Retinal Degeneration
Jasmina Cehajic-Kapetanovic, Johannes Birtel, Michelle E McClements, et al.
Genes
|
December 16, 2020
Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL
Susan M Downes, Tham Nguyen, Vicky Tai, et al.
Rheumatology Advances in Practice
|
August 22, 2019
An audit of the use of hydroxychloroquine in rheumatology clinics
Claudia Worth, Imran H Yusuf, Bethany Turner, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
July 7, 2023
New Imaging Technology for Simultaneous Multiwavelength-UWF Fundus Fluorescein Angiography and Indocyanine Green Angiography With Navigated Central and Peripheral SS-OCT
Francisco Javier Valentin Bravo, William Ayliffe, Sebastian Francis Eduardo Stanga, et al.
Retina (Philadelphia, Pa.)
|
December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology
Anthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Cells
|
August 26, 2023
The Role of Inflammation in Age-Related Macular Degeneration-Therapeutic Landscapes in Geographic Atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Monica L Hu, et al.
Genes
|
December 30, 2025
Expanding the Genetic Spectrum in <i>IMPG1</i> and <i>IMPG2</i> Retinopathy
Saoud Al-Khuzaei, Ahmed K Shalaby, Jing Yu, et al.
Frontiers in Neuroscience
|
July 16, 2024
Age-related macular degeneration: suitability of optogenetic therapy for geographic atrophy
Grace A Borchert, Hoda Shamsnajafabadi, Benjamin W J Ng, et al.
The British Journal of Ophthalmology
|
July 22, 2017
Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNA<sup>Lys</sup> (m.8340G>A) gene variant
Jaidip S Gill, Steven A Hardy, Emma L Blakely, et al.
The British Journal of Ophthalmology
|
June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophies
Ryan Combs, Georgina Hall, Katherine Payne, et al.
Page
of 14