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

Andrew R Webster

Showing results (141-150 of 372) with videos related to

Pageof 38
Sort By:
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2005
Autofluorescence imaging of choroidal neovascularization due to age-related macular degenerationSamantha S Dandekar, Sharon A Jenkins, Tunde Peto, et al.
Ophthalmology|October 15, 2018
Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease)Omar A Mahroo, Kamron N Khan, Genevieve Wright, et al.
European Journal of Human Genetics : EJHG|February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophyRyan Combs, Marion McAllister, Katherine Payne, et al.
Human Mutation|March 9, 2017
Single-base substitutions in the CHM promoter as a cause of choroideremiaAlina Radziwon, Gavin Arno, Dianna K Wheaton, et al.
The British Journal of Ophthalmology|July 4, 2019
Characterisation of microvascular abnormalities using OCT angiography in patients with biallelic variants in <i>USH2A</i> and <i>MYO7A</i>Ahmed M Hagag, Andreas Mitsios, Jasdeep S Gill, et al.
BMJ Open Ophthalmology|August 9, 2021
Prevalence of electronegative electroretinograms in a healthy adult cohortXiaofan Jiang, Taha Bhatti, Ambreen Tariq, et al.
JAMA Ophthalmology|June 10, 2016
Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3)Gavin Arno, Graham E Holder, Christina Chakarova, et al.
Investigative Ophthalmology & Visual Science|July 1, 2025
A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African AncestryWendy M Wong, Anthony G Robson, Rebecca A Baker, et al.
Ophthalmology|May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Pageof 38

Showing results (141-150 of 372) with videos related to

Sort By:
Pageof 38
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2005
Autofluorescence imaging of choroidal neovascularization due to age-related macular degenerationSamantha S Dandekar, Sharon A Jenkins, Tunde Peto, et al.
Ophthalmology|October 15, 2018
Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease)Omar A Mahroo, Kamron N Khan, Genevieve Wright, et al.
European Journal of Human Genetics : EJHG|February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophyRyan Combs, Marion McAllister, Katherine Payne, et al.
Human Mutation|March 9, 2017
Single-base substitutions in the CHM promoter as a cause of choroideremiaAlina Radziwon, Gavin Arno, Dianna K Wheaton, et al.
The British Journal of Ophthalmology|July 4, 2019
Characterisation of microvascular abnormalities using OCT angiography in patients with biallelic variants in <i>USH2A</i> and <i>MYO7A</i>Ahmed M Hagag, Andreas Mitsios, Jasdeep S Gill, et al.
BMJ Open Ophthalmology|August 9, 2021
Prevalence of electronegative electroretinograms in a healthy adult cohortXiaofan Jiang, Taha Bhatti, Ambreen Tariq, et al.
JAMA Ophthalmology|June 10, 2016
Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3)Gavin Arno, Graham E Holder, Christina Chakarova, et al.
Investigative Ophthalmology & Visual Science|July 1, 2025
A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African AncestryWendy M Wong, Anthony G Robson, Rebecca A Baker, et al.
Ophthalmology|May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Pageof 38