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M Lamey

Showing results (41-50 of 73) with videos related to

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Stem Cell Research|April 4, 2025
Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variantKhine 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 OCTRachael 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 RetinopathiesDanial 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 familyJuanita 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 ParametersSena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Ophthalmology. Retina|August 29, 2023
ReplyRachael 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> RetinopathyJason 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 AUTOFLUORESCENCERachael 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 AutofluorescenceRachael 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 SNRNP200Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Stem Cell Research|April 4, 2025
Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variantKhine 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 OCTRachael 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 RetinopathiesDanial 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 familyJuanita 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 ParametersSena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Ophthalmology. Retina|August 29, 2023
ReplyRachael 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> RetinopathyJason 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 AUTOFLUORESCENCERachael 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 AutofluorescenceRachael 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 SNRNP200Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
Pageof 8