Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anthony T Moore

Showing results (101-110 of 277) with videos related to

Pageof 28
Sort By:
Molecular Vision|May 8, 2009
Blue cone monochromacy: causative mutations and associated phenotypesJessica C Gardner, Michel Michaelides, Graham E Holder, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokersTiina Sepp, Jane C Khan, Deborah A Thurlby, et al.
Ophthalmic Genetics|October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataractVanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Progress in Retinal and Eye Research|May 14, 2016
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processesKamron N Khan, Omar A Mahroo, Rehna S Khan, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
A survey of DNA variation of C2ORF71 in probands with progressive autosomal recessive retinal degeneration and controlsPanagiotis I Sergouniotis, Zheng Li, Donna S Mackay, et al.
Ophthalmology. Retina|July 5, 2022
Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical ResultsMark Edward Pennesi, Paul Yang, David G Birch, et al.
Molecular Vision|April 21, 2010
Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathyEsther Meyer, Michel Michaelides, Louise J Tee, et al.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
Pageof 28

Showing results (101-110 of 277) with videos related to

Sort By:
Pageof 28
Molecular Vision|May 8, 2009
Blue cone monochromacy: causative mutations and associated phenotypesJessica C Gardner, Michel Michaelides, Graham E Holder, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokersTiina Sepp, Jane C Khan, Deborah A Thurlby, et al.
Ophthalmic Genetics|October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataractVanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Progress in Retinal and Eye Research|May 14, 2016
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processesKamron N Khan, Omar A Mahroo, Rehna S Khan, et al.
Retina (Philadelphia, Pa.)|December 3, 2009
"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiologyAnthony G Robson, Andrew R Webster, Michel Michaelides, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
A survey of DNA variation of C2ORF71 in probands with progressive autosomal recessive retinal degeneration and controlsPanagiotis I Sergouniotis, Zheng Li, Donna S Mackay, et al.
Ophthalmology. Retina|July 5, 2022
Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis: 1-Year Clinical ResultsMark Edward Pennesi, Paul Yang, David G Birch, et al.
Molecular Vision|April 21, 2010
Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathyEsther Meyer, Michel Michaelides, Louise J Tee, et al.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
Pageof 28