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 (1-10 of 372) with videos related to

Pageof 38
Sort By:
Journal of Occupational and Environmental Hygiene|March 25, 2005
Rapid assessment of microbial hazards in metalworking fluidsAndrew R Webster, JiYoung Lee, Rolf A Deininger
JAMA Ophthalmology|June 18, 2025
Recognizing Variants Prevalent in Particular AncestriesOmar A Mahroo, Siying Lin, Andrew R Webster
Investigative Ophthalmology & Visual Science|February 12, 2015
Efficacy and prognostic factors of response to carbonic anhydrase inhibitors in management of cystoid macular edema in retinitis pigmentosaGerald Liew, Anthony T Moore, Andrew R Webster, et al.
Ophthalmic Genetics|March 13, 2023
Typical best vitelliform dystrophy secondary to biallelic variants in BEST1Pankaja Dhoble, Anthony G Robson, Andrew R Webster, et al.
Current Opinion in Neurology|January 27, 2009
Update on Usher syndromeZubin Saihan, Andrew R Webster, Linda Luxon, et al.
Experimental Eye Research|March 11, 2014
The effect of the common c.2299delG mutation in USH2A on RNA splicingEva Lenassi, Zubin Saihan, Maria Bitner-Glindzicz, et al.
BMC Research Notes|December 12, 2013
An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case reportMichael Karampelas, Vasileios Soumplis, Dimitrios Karagiannis, et al.
Ophthalmic Genetics|August 24, 2021
A rare canonical splice-site variant in VPS13B causes attenuated Cohen syndromeMalena Daich Varela, Fabiana Louise Motta, Andrew R Webster, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|April 19, 2022
Whole Genome Sequencing Identifies a Partial Deletion of RTN4IP1 in a Patient With Isolated Optic AtrophyNeringa Jurkute, Gavin Arno, Andrew R Webster, et al.
Ophthalmic Genetics|September 4, 2008
The frequency of the H402 allele of CFH and its involvement with age-related maculopathy in an aged Black African Xhosa populationAri Ziskind, Soraya Bardien, Lize van der Merwe, et al.
Pageof 38

Showing results (1-10 of 372) with videos related to

Sort By:
Pageof 38
Journal of Occupational and Environmental Hygiene|March 25, 2005
Rapid assessment of microbial hazards in metalworking fluidsAndrew R Webster, JiYoung Lee, Rolf A Deininger
JAMA Ophthalmology|June 18, 2025
Recognizing Variants Prevalent in Particular AncestriesOmar A Mahroo, Siying Lin, Andrew R Webster
Investigative Ophthalmology & Visual Science|February 12, 2015
Efficacy and prognostic factors of response to carbonic anhydrase inhibitors in management of cystoid macular edema in retinitis pigmentosaGerald Liew, Anthony T Moore, Andrew R Webster, et al.
Ophthalmic Genetics|March 13, 2023
Typical best vitelliform dystrophy secondary to biallelic variants in BEST1Pankaja Dhoble, Anthony G Robson, Andrew R Webster, et al.
Current Opinion in Neurology|January 27, 2009
Update on Usher syndromeZubin Saihan, Andrew R Webster, Linda Luxon, et al.
Experimental Eye Research|March 11, 2014
The effect of the common c.2299delG mutation in USH2A on RNA splicingEva Lenassi, Zubin Saihan, Maria Bitner-Glindzicz, et al.
BMC Research Notes|December 12, 2013
An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case reportMichael Karampelas, Vasileios Soumplis, Dimitrios Karagiannis, et al.
Ophthalmic Genetics|August 24, 2021
A rare canonical splice-site variant in VPS13B causes attenuated Cohen syndromeMalena Daich Varela, Fabiana Louise Motta, Andrew R Webster, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|April 19, 2022
Whole Genome Sequencing Identifies a Partial Deletion of RTN4IP1 in a Patient With Isolated Optic AtrophyNeringa Jurkute, Gavin Arno, Andrew R Webster, et al.
Ophthalmic Genetics|September 4, 2008
The frequency of the H402 allele of CFH and its involvement with age-related maculopathy in an aged Black African Xhosa populationAri Ziskind, Soraya Bardien, Lize van der Merwe, et al.
Pageof 38