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Anthony T Moore

Showing results (51-60 of 277) with videos related to

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Investigative Ophthalmology & Visual Science|March 27, 2003
An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4Michel Michaelides, Samantha Johnson, Arabella Poulson, et al.
Genes|May 10, 2020
Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital CataractVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 22, 2015
Electroretinogram assessment of children with sensorineural hearing loss: implications for screeningStephanie K West, Maya Hindocha, Chris R Hogg, et al.
Investigative Ophthalmology & Visual Science|December 28, 2013
Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod functionAndrew Stockman, G Bruce Henning, Michel Michaelides, et al.
The British Journal of Ophthalmology|May 12, 2011
High-resolution optical coherence tomography imaging in KCNV2 retinopathyPanagiotis I Sergouniotis, Graham E Holder, Anthony G Robson, et al.
Ophthalmology|December 21, 2011
Retinal structure, function, and molecular pathologic features in gyrate atrophyPanagiotis I Sergouniotis, Alice E Davidson, Eva Lenassi, et al.
The British Journal of Ophthalmology|February 25, 2016
Preserved visual function in retinal dystrophy due to hypomorphic <i>RPE65</i> mutationsSarah Hull, Graham E Holder, Anthony G Robson, et al.
Eye (London, England)|June 24, 2018
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataractVanita Berry, Alexander C W Ionides, Nikolas Pontikos, et al.
Ophthalmology|February 23, 2010
Macular function assessed by microperimetry in patients with enhanced S-cone syndromeElliott H Sohn, Fred K Chen, Gary S Rubin, et al.
Retina (Philadelphia, Pa.)|June 8, 2017
NORMAL ELECTROOCULOGRAPHY IN BEST DISEASE AND AUTOSOMAL RECESSIVE BESTROPHINOPATHYKamron N Khan, Farrah Islam, Graham E Holder, et al.
Pageof 28

Showing results (51-60 of 277) with videos related to

Sort By:
Pageof 28
Investigative Ophthalmology & Visual Science|March 27, 2003
An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4Michel Michaelides, Samantha Johnson, Arabella Poulson, et al.
Genes|May 10, 2020
Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital CataractVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 22, 2015
Electroretinogram assessment of children with sensorineural hearing loss: implications for screeningStephanie K West, Maya Hindocha, Chris R Hogg, et al.
Investigative Ophthalmology & Visual Science|December 28, 2013
Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod functionAndrew Stockman, G Bruce Henning, Michel Michaelides, et al.
The British Journal of Ophthalmology|May 12, 2011
High-resolution optical coherence tomography imaging in KCNV2 retinopathyPanagiotis I Sergouniotis, Graham E Holder, Anthony G Robson, et al.
Ophthalmology|December 21, 2011
Retinal structure, function, and molecular pathologic features in gyrate atrophyPanagiotis I Sergouniotis, Alice E Davidson, Eva Lenassi, et al.
The British Journal of Ophthalmology|February 25, 2016
Preserved visual function in retinal dystrophy due to hypomorphic <i>RPE65</i> mutationsSarah Hull, Graham E Holder, Anthony G Robson, et al.
Eye (London, England)|June 24, 2018
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataractVanita Berry, Alexander C W Ionides, Nikolas Pontikos, et al.
Ophthalmology|February 23, 2010
Macular function assessed by microperimetry in patients with enhanced S-cone syndromeElliott H Sohn, Fred K Chen, Gary S Rubin, et al.
Retina (Philadelphia, Pa.)|June 8, 2017
NORMAL ELECTROOCULOGRAPHY IN BEST DISEASE AND AUTOSOMAL RECESSIVE BESTROPHINOPATHYKamron N Khan, Farrah Islam, Graham E Holder, et al.
Pageof 28