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Documenta Ophthalmologica. Advances in Ophthalmology
|
November 18, 2018
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)
Fred K Chen, Xiao Zhang, Jonathan Eintracht, et al.
Translational Vision Science & Technology
|
June 10, 2021
Retinal Differential Light Sensitivity Variation Across the Macula in Healthy Subjects: Importance of Cone Separation and Loci Eccentricity
Danuta M Sampson, Danial Roshandel, Avenell L Chew, et al.
Ophthalmic Genetics
|
September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathy
Danial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Ophthalmic Genetics
|
February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathy
Zhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine
|
July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect
Di Huang, Jennifer A Thompson, Jason Charng, et al.
Investigative Ophthalmology & Visual Science
|
April 14, 2026
ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
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Showing results (11-20 of 16) with videos related to
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This site can display upto 16 results.
Documenta Ophthalmologica. Advances in Ophthalmology
|
November 18, 2018
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)
Fred K Chen, Xiao Zhang, Jonathan Eintracht, et al.
Translational Vision Science & Technology
|
June 10, 2021
Retinal Differential Light Sensitivity Variation Across the Macula in Healthy Subjects: Importance of Cone Separation and Loci Eccentricity
Danuta M Sampson, Danial Roshandel, Avenell L Chew, et al.
Ophthalmic Genetics
|
September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathy
Danial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Ophthalmic Genetics
|
February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathy
Zhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine
|
July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect
Di Huang, Jennifer A Thompson, Jason Charng, et al.
Investigative Ophthalmology & Visual Science
|
April 14, 2026
ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
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of 2