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 G Robson

Showing results (41-50 of 188) with videos related to

Pageof 19
Sort By:
Acta Ophthalmologica|May 22, 2015
Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11Irina Balikova, Anthony G Robson, Graham E Holder, et al.
Acta Ophthalmologica|December 30, 2014
Exome sequencing reveals ADAM9 mutations in a child with cone-rod dystrophySarah Hull, Gavin Arno, Vincent Plagnol, et al.
European Journal of Ophthalmology|August 19, 2020
Long-term follow-up of a case of posterior microphthalmos (PRSS56) with hyperautofluorescent retinal pigment epithelial depositsPiyali Sen, Anthony G Robson, Andrew R Webster, et al.
Investigative Ophthalmology & Visual Science|August 18, 2012
Macular pigment parameters in patients with macular telangiectasia (MacTel) and normal subjects: implications of a novel analysisSimona Degli Esposti, Catherine Egan, Catey Bunce, et al.
Retina (Philadelphia, Pa.)|January 5, 2018
PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY: Detailed Clinical Study of a Large CohortOlajumoke A Shona, Farrah Islam, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 27, 2023
The diagnostic accuracy of photopic negative responses evoked by broadband and chromatic stimuli in a clinically heterogeneous populationShaun M Leo, Magella M Neveu, Patrick Yu-Wai-Man, et al.
Clinical & Experimental Ophthalmology|February 23, 2008
A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutationSobha Sivaprasad, Boom Ting Kung, Anthony G Robson, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Autofluorescence findings in acute exudative polymorphous vitelliform maculopathyVeronika Vaclavik, Kenneth G-J Ooi, Alan C Bird, et al.
American Journal of Ophthalmology|January 30, 2007
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutationAndrew Scott, Nicholas G Strouthidis, Anthony G Robson, et al.
Pageof 19

Showing results (41-50 of 188) with videos related to

Sort By:
Pageof 19
Acta Ophthalmologica|May 22, 2015
Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11Irina Balikova, Anthony G Robson, Graham E Holder, et al.
Acta Ophthalmologica|December 30, 2014
Exome sequencing reveals ADAM9 mutations in a child with cone-rod dystrophySarah Hull, Gavin Arno, Vincent Plagnol, et al.
European Journal of Ophthalmology|August 19, 2020
Long-term follow-up of a case of posterior microphthalmos (PRSS56) with hyperautofluorescent retinal pigment epithelial depositsPiyali Sen, Anthony G Robson, Andrew R Webster, et al.
Investigative Ophthalmology & Visual Science|August 18, 2012
Macular pigment parameters in patients with macular telangiectasia (MacTel) and normal subjects: implications of a novel analysisSimona Degli Esposti, Catherine Egan, Catey Bunce, et al.
Retina (Philadelphia, Pa.)|January 5, 2018
PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY: Detailed Clinical Study of a Large CohortOlajumoke A Shona, Farrah Islam, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 27, 2023
The diagnostic accuracy of photopic negative responses evoked by broadband and chromatic stimuli in a clinically heterogeneous populationShaun M Leo, Magella M Neveu, Patrick Yu-Wai-Man, et al.
Clinical & Experimental Ophthalmology|February 23, 2008
A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutationSobha Sivaprasad, Boom Ting Kung, Anthony G Robson, 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.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Autofluorescence findings in acute exudative polymorphous vitelliform maculopathyVeronika Vaclavik, Kenneth G-J Ooi, Alan C Bird, et al.
American Journal of Ophthalmology|January 30, 2007
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutationAndrew Scott, Nicholas G Strouthidis, Anthony G Robson, et al.
Pageof 19