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 (151-160 of 372) with videos related to

Pageof 38
Sort By:
European Journal of Medical Genetics|July 2, 2013
A clinical molecular genetic service for United Kingdom families with choroideraemiaSimon C Ramsden, Anna O'Grady, Tracy Fletcher, et al.
Ophthalmology|November 13, 2015
Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in HumansRola Ba-Abbad, Gavin Arno, Keren Carss, et al.
Eye (London, England)|August 29, 2019
A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutationsSancy Low, Ryian Mohamed, Alice Davidson, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|August 29, 2013
ABCA4 gene screening by next-generation sequencing in a British cohortKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trialsJonathan Aboshiha, Vy Luong, Jill Cowing, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Investigative Ophthalmology & Visual Science|September 12, 2025
Selective Impairment of Rod-Driven Vision in Vitamin A Deficiency: Insights From Examining the Effect of Desensitizing BackgroundsMegan Margetts, Remi Rufus-Toye, Xiaofan Jiang, et al.
Molecular Vision|January 21, 2010
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humansRobert H Henderson, Zheng Li, Mai M Abd El Aziz, et al.
JMIR Formative Research|January 31, 2022
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility StudyRose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, et al.
Pageof 38

Showing results (151-160 of 372) with videos related to

Sort By:
Pageof 38
European Journal of Medical Genetics|July 2, 2013
A clinical molecular genetic service for United Kingdom families with choroideraemiaSimon C Ramsden, Anna O'Grady, Tracy Fletcher, et al.
Ophthalmology|November 13, 2015
Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in HumansRola Ba-Abbad, Gavin Arno, Keren Carss, et al.
Eye (London, England)|August 29, 2019
A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutationsSancy Low, Ryian Mohamed, Alice Davidson, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|August 29, 2013
ABCA4 gene screening by next-generation sequencing in a British cohortKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|August 30, 2014
Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trialsJonathan Aboshiha, Vy Luong, Jill Cowing, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Investigative Ophthalmology & Visual Science|September 12, 2025
Selective Impairment of Rod-Driven Vision in Vitamin A Deficiency: Insights From Examining the Effect of Desensitizing BackgroundsMegan Margetts, Remi Rufus-Toye, Xiaofan Jiang, et al.
Molecular Vision|January 21, 2010
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humansRobert H Henderson, Zheng Li, Mai M Abd El Aziz, et al.
JMIR Formative Research|January 31, 2022
Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility StudyRose M Gilbert, Dayyanah Sumodhee, Nikolas Pontikos, et al.
Pageof 38