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Anthony T Moore

Showing results (171-180 of 277) with videos related to

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Translational Vision Science & Technology|August 22, 2020
Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular DegenerationKamron N Khan, Shyamanga Borooah, Leonardo Lando, et al.
Investigative Ophthalmology & Visual Science|March 26, 2011
Integrity of the cone photoreceptor mosaic in oligocone trichromacyMichel Michaelides, Jungtae Rha, Elise W Dees, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Ophthalmology|February 1, 2014
Detailed phenotypic and genotypic characterization of bietti crystalline dystrophyStephanie Halford, Gerald Liew, Donna S Mackay, et al.
American Journal of Ophthalmology|August 20, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and functionKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
American Journal of Human Genetics|November 15, 2016
Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment DysgenesisSek-Shir Cheong, Lisa Hentschel, Alice E Davidson, et al.
American Journal of Human Genetics|March 15, 2006
Mutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndromeIrene A Aligianis, Neil V Morgan, Marina Mione, et al.
Scientific Reports|August 10, 2017
Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locusValentina Cipriani, Raquel S Silva, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Pageof 28

Showing results (171-180 of 277) with videos related to

Sort By:
Pageof 28
Translational Vision Science & Technology|August 22, 2020
Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular DegenerationKamron N Khan, Shyamanga Borooah, Leonardo Lando, et al.
Investigative Ophthalmology & Visual Science|March 26, 2011
Integrity of the cone photoreceptor mosaic in oligocone trichromacyMichel Michaelides, Jungtae Rha, Elise W Dees, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Ophthalmology|February 1, 2014
Detailed phenotypic and genotypic characterization of bietti crystalline dystrophyStephanie Halford, Gerald Liew, Donna S Mackay, et al.
American Journal of Ophthalmology|August 20, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and functionKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
American Journal of Human Genetics|November 15, 2016
Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment DysgenesisSek-Shir Cheong, Lisa Hentschel, Alice E Davidson, et al.
American Journal of Human Genetics|March 15, 2006
Mutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndromeIrene A Aligianis, Neil V Morgan, Marina Mione, et al.
Scientific Reports|August 10, 2017
Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locusValentina Cipriani, Raquel S Silva, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Pageof 28