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

Rando Allikmets

Showing results (111-120 of 180) with videos related to

Pageof 18
Sort By:
Plos One|September 7, 2012
Identification of a potential susceptibility locus for macular telangiectasia type 2Nancy L Parmalee, Carl Schubert, Maria Figueroa, et al.
Investigative Ophthalmology & Visual Science|May 27, 2008
ATM gene variants in patients with idiopathic perifoveal telangiectasiaIrene A Barbazetto, Miia Room, Nicholas A Yannuzzi, et al.
Human Mutation|January 4, 2017
In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy CasesStéphanie S Cornelis, Nathalie M Bax, Jana Zernant, 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|March 29, 2014
Quantitative fundus autofluorescence in recessive Stargardt diseaseTomas R Burke, Tobias Duncker, Russell L Woods, et al.
JCI Insight|October 20, 2022
A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt diseaseMasha Kolesnikova, Jin Kyun Oh, Jiali Wang, et al.
American Journal of Ophthalmology|September 17, 2011
Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosaRoyce W S Chen, Jonathan P Greenberg, Margot A Lazow, et al.
Human Mutation|July 29, 2014
Genetic and clinical analysis of ABCA4-associated disease in African American patientsJana Zernant, Frederick T Collison, Winston Lee, et al.
Human Genomics|August 3, 2011
Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degenerationGregory S Hageman, Karen Gehrs, Serguei Lejnine, et al.
American Journal of Ophthalmology|May 24, 2020
Optical Gap Biomarker in Cone-Dominant Retinal DystrophyJin Kyun Oh, Joseph Ryu, Jose Ronaldo Lima de Carvalho, et al.
Pageof 18

Showing results (111-120 of 180) with videos related to

Sort By:
Pageof 18
Plos One|September 7, 2012
Identification of a potential susceptibility locus for macular telangiectasia type 2Nancy L Parmalee, Carl Schubert, Maria Figueroa, et al.
Investigative Ophthalmology & Visual Science|May 27, 2008
ATM gene variants in patients with idiopathic perifoveal telangiectasiaIrene A Barbazetto, Miia Room, Nicholas A Yannuzzi, et al.
Human Mutation|January 4, 2017
In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy CasesStéphanie S Cornelis, Nathalie M Bax, Jana Zernant, 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|March 29, 2014
Quantitative fundus autofluorescence in recessive Stargardt diseaseTomas R Burke, Tobias Duncker, Russell L Woods, et al.
JCI Insight|October 20, 2022
A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt diseaseMasha Kolesnikova, Jin Kyun Oh, Jiali Wang, et al.
American Journal of Ophthalmology|September 17, 2011
Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosaRoyce W S Chen, Jonathan P Greenberg, Margot A Lazow, et al.
Human Mutation|July 29, 2014
Genetic and clinical analysis of ABCA4-associated disease in African American patientsJana Zernant, Frederick T Collison, Winston Lee, et al.
Human Genomics|August 3, 2011
Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degenerationGregory S Hageman, Karen Gehrs, Serguei Lejnine, et al.
American Journal of Ophthalmology|May 24, 2020
Optical Gap Biomarker in Cone-Dominant Retinal DystrophyJin Kyun Oh, Joseph Ryu, Jose Ronaldo Lima de Carvalho, et al.
Pageof 18