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 (161-170 of 372) with videos related to

Pageof 38
Sort By:
Investigative Ophthalmology & Visual Science|June 27, 2006
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunctionMichel Michaelides, Sharon A Jenkins, Milam A Brantley, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth CohortPirro G Hysi, Claire L Simpson, Yvonne K Y Fok, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Ophthalmology. Retina|March 14, 2025
Best Vitelliform Macular Dystrophy Natural History Study Report 2: Fundus Autofluorescence and OCTYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 38

Showing results (161-170 of 372) with videos related to

Sort By:
Pageof 38
Investigative Ophthalmology & Visual Science|June 27, 2006
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunctionMichel Michaelides, Sharon A Jenkins, Milam A Brantley, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth CohortPirro G Hysi, Claire L Simpson, Yvonne K Y Fok, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Ophthalmology. Retina|March 14, 2025
Best Vitelliform Macular Dystrophy Natural History Study Report 2: Fundus Autofluorescence and OCTYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 38