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Enid Chelva

Showing results (11-20 of 16) with videos related to

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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 EccentricityDanuta 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 retinopathyDanial 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 retinopathyZhiqin 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 defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Investigative Ophthalmology & Visual Science|April 14, 2026
ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological FindingsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.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 EccentricityDanuta 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 retinopathyDanial 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 retinopathyZhiqin 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 defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Investigative Ophthalmology & Visual Science|April 14, 2026
ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological FindingsRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Pageof 2