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

Rola Ba-Abbad

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
Ophthalmic Genetics|May 20, 2024
Revisiting molecular diagnosis in a family with retinitis pigmentosa: integrating deep phenotyping and bioinformatic analysisRola Ba-Abbad
Cornea|December 19, 2008
Penetrating keratoplasty for keratoconus with or without vernal keratoconjunctivitisMichael D Wagoner, Rola Ba-Abbad,
Ophthalmic Genetics|May 29, 2023
Phenotypic and genotypic features of <i>POC1B</i>-associated cone dystrophyTariq A Alzahem, Abdulwahab AlTheeb, Rola Ba-Abbad
Genes|June 27, 2024
The Clinical and Mutational Spectrum of Bardet-Biedl Syndrome in Saudi ArabiaDoaa Milibari, Sawsan R Nowilaty, Rola Ba-Abbad
Ophthalmic Genetics|April 15, 2024
<i>PRPS1</i>-associated retinopathy: a diagnostic odysseyTariq A Alzahem, Abdulwahab AlTheeb, Rola Ba-Abbad
Ophthalmic Genetics|April 20, 2026
Unusual presentation of cone dysfunction consequent upon a homozygous <i>FAM161A</i> variantJinan Alhamad, Enas Magharbil, Sawsan R Nowilaty, et al.
Ophthalmology|March 21, 2007
Corneal transplant survival after onset of severe endothelial rejectionMichael D Wagoner, Rola Ba-Abbad, John E Sutphin, et al.
Ophthalmic Genetics|May 8, 2019
Rod-cone dystrophy associated with the Gly167Asp variant in PRPH2Rola Ba-Abbad, Anthony G Robson, Becky MacPhee, et al.
Retinal Cases & Brief Reports|June 17, 2020
MONOZYGOTIC TWINS DISCORDANT FOR ASYMMETRIC PIGMENTED PARAVENOUS CHORIORETINAL ATROPHYNaomi Fischer, Emma Duignan, Anthony G Robson, et al.
Ophthalmic Genetics|January 5, 2020
Macular maldevelopment in <i>ATF6</i>-mediated retinal dysfunctionMarkus Ritter, Gavin Arno, Rola Ba-Abbad, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Ophthalmic Genetics|May 20, 2024
Revisiting molecular diagnosis in a family with retinitis pigmentosa: integrating deep phenotyping and bioinformatic analysisRola Ba-Abbad
Cornea|December 19, 2008
Penetrating keratoplasty for keratoconus with or without vernal keratoconjunctivitisMichael D Wagoner, Rola Ba-Abbad,
Ophthalmic Genetics|May 29, 2023
Phenotypic and genotypic features of <i>POC1B</i>-associated cone dystrophyTariq A Alzahem, Abdulwahab AlTheeb, Rola Ba-Abbad
Genes|June 27, 2024
The Clinical and Mutational Spectrum of Bardet-Biedl Syndrome in Saudi ArabiaDoaa Milibari, Sawsan R Nowilaty, Rola Ba-Abbad
Ophthalmic Genetics|April 15, 2024
<i>PRPS1</i>-associated retinopathy: a diagnostic odysseyTariq A Alzahem, Abdulwahab AlTheeb, Rola Ba-Abbad
Ophthalmic Genetics|April 20, 2026
Unusual presentation of cone dysfunction consequent upon a homozygous <i>FAM161A</i> variantJinan Alhamad, Enas Magharbil, Sawsan R Nowilaty, et al.
Ophthalmology|March 21, 2007
Corneal transplant survival after onset of severe endothelial rejectionMichael D Wagoner, Rola Ba-Abbad, John E Sutphin, et al.
Ophthalmic Genetics|May 8, 2019
Rod-cone dystrophy associated with the Gly167Asp variant in PRPH2Rola Ba-Abbad, Anthony G Robson, Becky MacPhee, et al.
Retinal Cases & Brief Reports|June 17, 2020
MONOZYGOTIC TWINS DISCORDANT FOR ASYMMETRIC PIGMENTED PARAVENOUS CHORIORETINAL ATROPHYNaomi Fischer, Emma Duignan, Anthony G Robson, et al.
Ophthalmic Genetics|January 5, 2020
Macular maldevelopment in <i>ATF6</i>-mediated retinal dysfunctionMarkus Ritter, Gavin Arno, Rola Ba-Abbad, et al.
Pageof 4