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

G Robson

Showing results (391-400 of 456) with videos related to

Pageof 46
Sort By:
Human Mutation|January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophyAlice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Ophthalmology. Retina|June 18, 2023
CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural HistoryMalena Daich Varela, Emma S Duignan, Samantha R De Silva, et al.
Advanced Materials (Deerfield Beach, Fla.)|August 29, 2024
Scalable Atomic Arrays for Spin-Based Quantum Computers in SiliconAlexander M Jakob, Simon G Robson, Hannes R Firgau, et al.
Trials|May 14, 2016
Paclitaxel-coated balloon fistuloplasty versus plain balloon fistuloplasty only to preserve the patency of arteriovenous fistulae used for haemodialysis (PAVE): study protocol for a randomised controlled trialNarayan Karunanithy, Irene Rebollo Mesa, Anthony Dorling, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 31, 2025
ISCEV standard full-field ERG reference limits from 407 healthy subjects, derived from transference and validation of reference data between electrode types and centresRebecca A Baker, Shaun M Leo, William I N Clowes, et al.
Ophthalmology. Retina|January 14, 2020
Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for TherapyGenevieve A Wright, Michalis Georgiou, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
Translational Vision Science & Technology|September 30, 2022
Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field ElectroretinographySophie L Glinton, Antonio Calcagni, Watjana Lilaonitkul, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Pageof 46

Showing results (391-400 of 456) with videos related to

Sort By:
Pageof 46
Human Mutation|January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophyAlice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Ophthalmology. Retina|June 18, 2023
CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural HistoryMalena Daich Varela, Emma S Duignan, Samantha R De Silva, et al.
Advanced Materials (Deerfield Beach, Fla.)|August 29, 2024
Scalable Atomic Arrays for Spin-Based Quantum Computers in SiliconAlexander M Jakob, Simon G Robson, Hannes R Firgau, et al.
Trials|May 14, 2016
Paclitaxel-coated balloon fistuloplasty versus plain balloon fistuloplasty only to preserve the patency of arteriovenous fistulae used for haemodialysis (PAVE): study protocol for a randomised controlled trialNarayan Karunanithy, Irene Rebollo Mesa, Anthony Dorling, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 31, 2025
ISCEV standard full-field ERG reference limits from 407 healthy subjects, derived from transference and validation of reference data between electrode types and centresRebecca A Baker, Shaun M Leo, William I N Clowes, et al.
Ophthalmology. Retina|January 14, 2020
Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for TherapyGenevieve A Wright, Michalis Georgiou, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
Translational Vision Science & Technology|September 30, 2022
Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field ElectroretinographySophie L Glinton, Antonio Calcagni, Watjana Lilaonitkul, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Pageof 46