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

Michalis Georgiou

Showing results (41-50 of 96) with videos related to

Pageof 10
Sort By:
American Journal of Ophthalmology|December 9, 2019
Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease SymmetryMichalis Georgiou, Thomas Kane, Preena Tanna, et al.
Ophthalmic Genetics|August 14, 2020
Macula-predominant retinopathy associated with biallelic variants in <i>RDH12</i>Rola Ba-Abbad, Gavin Arno, Anthony G Robson, et al.
The British Journal of Ophthalmology|February 12, 2020
Prospective exploratory study to assess the safety and efficacy of aflibercept in cystoid macular oedema associated with retinitis pigmentosaStacey A Strong, Tunde Peto, Catey Bunce, et al.
Orphanet Journal of Rare Diseases|November 27, 2020
The genetic landscape of crystallins in congenital cataractVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Translational Vision Science & Technology|August 25, 2020
Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in <i>CNGA3-</i> and <i>CNGB3</i>-Associated AchromatopsiaMichalis Georgiou, Katie M Litts, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science|March 24, 2020
Photoreceptor Structure in GNAT2-Associated AchromatopsiaMichalis Georgiou, Navjit Singh, Thomas Kane, et al.
Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
The British Journal of Ophthalmology|May 25, 2021
Novel disease-causing variant in <i>RDH12</i> presenting with autosomal dominant retinitis pigmentosaManickam Nick Muthiah, Angelos Kalitzeos, Kate Oprych, et al.
Investigative Ophthalmology & Visual Science|September 22, 2020
Long-Term Investigation of Retinal Function in Patients with AchromatopsiaMichalis Georgiou, Navjit Singh, Thomas Kane, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
American Journal of Ophthalmology|December 9, 2019
Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease SymmetryMichalis Georgiou, Thomas Kane, Preena Tanna, et al.
Ophthalmic Genetics|August 14, 2020
Macula-predominant retinopathy associated with biallelic variants in <i>RDH12</i>Rola Ba-Abbad, Gavin Arno, Anthony G Robson, et al.
The British Journal of Ophthalmology|February 12, 2020
Prospective exploratory study to assess the safety and efficacy of aflibercept in cystoid macular oedema associated with retinitis pigmentosaStacey A Strong, Tunde Peto, Catey Bunce, et al.
Orphanet Journal of Rare Diseases|November 27, 2020
The genetic landscape of crystallins in congenital cataractVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
Eye (London, England)|May 22, 2026
Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with four rod phototransduction genesVishanna Balbirsingh, Shaima A Hashem, Michalis Georgiou, et al.
Translational Vision Science & Technology|August 25, 2020
Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in <i>CNGA3-</i> and <i>CNGB3</i>-Associated AchromatopsiaMichalis Georgiou, Katie M Litts, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science|March 24, 2020
Photoreceptor Structure in GNAT2-Associated AchromatopsiaMichalis Georgiou, Navjit Singh, Thomas Kane, et al.
Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
The British Journal of Ophthalmology|May 25, 2021
Novel disease-causing variant in <i>RDH12</i> presenting with autosomal dominant retinitis pigmentosaManickam Nick Muthiah, Angelos Kalitzeos, Kate Oprych, et al.
Investigative Ophthalmology & Visual Science|September 22, 2020
Long-Term Investigation of Retinal Function in Patients with AchromatopsiaMichalis Georgiou, Navjit Singh, Thomas Kane, et al.
Pageof 10