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Stem Cell Research
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April 4, 2025
Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variant
Khine Zaw, Milan Fernando, Dan Zhang, et al.
Ophthalmology. Retina
|
May 20, 2023
Analysis of the Outer Retinal Bands in ABCA4 and PRPH2-Associated Retinopathy using OCT
Rachael C Heath Jeffery, Johnny Lo, Jennifer A Thompson, et al.
Translational Vision Science & Technology
|
May 18, 2021
Multimodal Retinal Imaging and Microperimetry Reveal a Novel Phenotype and Potential Trial End Points in CRB1-Associated Retinopathies
Danial Roshandel, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Ophthalmic Genetics
|
October 13, 2020
Progressive sector retinitis pigmentosa due to c.440G>T mutation in <i>SAG</i> in an Australian family
Juanita Pappalardo, Rachael C Heath Jeffery, Jennifer A Thompson, et al.
Genes
|
February 26, 2025
Retinal Disease Variability in Female Carriers of <i>RPGR</i> Variants Associated with Retinitis Pigmentosa: Clinical and Genetic Parameters
Sena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Ophthalmology. Retina
|
August 29, 2023
Reply
Rachael C Heath Jeffery, Johnny Lo, Jennifer A Thompson, et al.
Translational Vision Science & Technology
|
September 25, 2020
Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in <i>USH2A</i> Retinopathy
Jason Charng, Tina M Lamey, Jennifer A Thompson, et al.
Retina (Philadelphia, Pa.)
|
March 28, 2022
SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Ophthalmology Science
|
October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus Autofluorescence
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Stem Cell Research
|
January 11, 2021
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200
Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
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of 8
Search research articles
Search
Showing results (41-50 of 73) with videos related to
Sort By:
Page
of 8
Stem Cell Research
|
April 4, 2025
Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variant
Khine Zaw, Milan Fernando, Dan Zhang, et al.
Ophthalmology. Retina
|
May 20, 2023
Analysis of the Outer Retinal Bands in ABCA4 and PRPH2-Associated Retinopathy using OCT
Rachael C Heath Jeffery, Johnny Lo, Jennifer A Thompson, et al.
Translational Vision Science & Technology
|
May 18, 2021
Multimodal Retinal Imaging and Microperimetry Reveal a Novel Phenotype and Potential Trial End Points in CRB1-Associated Retinopathies
Danial Roshandel, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Ophthalmic Genetics
|
October 13, 2020
Progressive sector retinitis pigmentosa due to c.440G>T mutation in <i>SAG</i> in an Australian family
Juanita Pappalardo, Rachael C Heath Jeffery, Jennifer A Thompson, et al.
Genes
|
February 26, 2025
Retinal Disease Variability in Female Carriers of <i>RPGR</i> Variants Associated with Retinitis Pigmentosa: Clinical and Genetic Parameters
Sena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Ophthalmology. Retina
|
August 29, 2023
Reply
Rachael C Heath Jeffery, Johnny Lo, Jennifer A Thompson, et al.
Translational Vision Science & Technology
|
September 25, 2020
Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in <i>USH2A</i> Retinopathy
Jason Charng, Tina M Lamey, Jennifer A Thompson, et al.
Retina (Philadelphia, Pa.)
|
March 28, 2022
SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Ophthalmology Science
|
October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus Autofluorescence
Rachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Stem Cell Research
|
January 11, 2021
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200
Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
Page
of 8