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Anthony T Moore

Showing results (191-200 of 277) with videos related to

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American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
JAMA Ophthalmology|June 4, 2016
Molecular and Clinical Findings in Patients With Knobloch SyndromeSarah Hull, Gavin Arno, Cristy A Ku, et al.
American Journal of Human Genetics|May 6, 2014
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophyPanagiotis I Sergouniotis, Christina Chakarova, Cian Murphy, et al.
JAMA Ophthalmology|May 31, 2014
Expansion of ocular phenotypic features associated with mutations in ADAMTS18Aman Chandra, Gavin Arno, Kathleen Williamson, et al.
The British Journal of Ophthalmology|January 26, 2021
Association of ambient air pollution with age-related macular degeneration and retinal thickness in UK BiobankSharon Y L Chua, Alasdair Warwick, Tunde Peto, et al.
Human Mutation|February 3, 2019
Unique noncoding variants upstream of PRDM13 are associated with a spectrum of developmental retinal dystrophies including progressive bifocal chorioretinal atrophyRaquel S Silva, Gavin Arno, Valentina Cipriani, et al.
American Journal of Ophthalmology|May 19, 2015
Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl SyndromeSophie Scheidecker, Sarah Hull, Yaumara Perdomo, et al.
Pageof 28

Showing results (191-200 of 277) with videos related to

Sort By:
Pageof 28
American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
JAMA Ophthalmology|June 4, 2016
Molecular and Clinical Findings in Patients With Knobloch SyndromeSarah Hull, Gavin Arno, Cristy A Ku, et al.
American Journal of Human Genetics|May 6, 2014
Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophyPanagiotis I Sergouniotis, Christina Chakarova, Cian Murphy, et al.
JAMA Ophthalmology|May 31, 2014
Expansion of ocular phenotypic features associated with mutations in ADAMTS18Aman Chandra, Gavin Arno, Kathleen Williamson, et al.
The British Journal of Ophthalmology|January 26, 2021
Association of ambient air pollution with age-related macular degeneration and retinal thickness in UK BiobankSharon Y L Chua, Alasdair Warwick, Tunde Peto, et al.
Human Mutation|February 3, 2019
Unique noncoding variants upstream of PRDM13 are associated with a spectrum of developmental retinal dystrophies including progressive bifocal chorioretinal atrophyRaquel S Silva, Gavin Arno, Valentina Cipriani, et al.
American Journal of Ophthalmology|May 19, 2015
Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl SyndromeSophie Scheidecker, Sarah Hull, Yaumara Perdomo, et al.
Pageof 28