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Samer Khateb

Showing results (31-40 of 70) with videos related to

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Investigative Ophthalmology & Visual Science|August 18, 2021
Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular DegenerationBatya Rinsky, Gala Beykin, Michelle Grunin, et al.
Journal of Clinical Medicine|November 27, 2024
Evaluation of Retinal and Posterior Segment Vascular Changes Due to Systemic Hypoxia Using Optical Coherence Tomography AngiographyNadav Levinger, Nir Erdinest, Ayman Abu Rmeileh, et al.
Investigative Ophthalmology & Visual Science|March 1, 2018
The Genetics of Usher Syndrome in the Israeli and Palestinian PopulationsAyat Khalaileh, Alaa Abu-Diab, Tamar Ben-Yosef, et al.
Journal of Clinical Medicine|March 27, 2025
Anterior Segment Characteristics and Quality of Life of Patients with Central Serous ChorioretinopathyHadas Ben-Eli, Tal Asher, Rivkah Lender, et al.
Molecular Vision|April 11, 2022
Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genesSamer Khateb, Aya Shemesh, Ashly Offenheim, et al.
Medicine|January 10, 2026
Evaluating a novel triangular suture technique for scleral support of dislocated intraocular lenses following cataract surgery: A retrospective cohort studyNir Erdinest, Michael Tabi, Or Shmueli, et al.
Translational Vision Science & Technology|March 1, 2023
Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in MiceAlaa Abu-Diab, Prakadeeswari Gopalakrishnan, Chen Matsevich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humansSamer Khateb, Björn Kowalewski, Nicola Bedoni, et al.
JAMA Ophthalmology|April 19, 2019
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6BSamer Khateb, Marco Nassisi, Kinga M Bujakowska, et al.
Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Investigative Ophthalmology & Visual Science|August 18, 2021
Analysis of the Aqueous Humor Proteome in Patients With Age-Related Macular DegenerationBatya Rinsky, Gala Beykin, Michelle Grunin, et al.
Journal of Clinical Medicine|November 27, 2024
Evaluation of Retinal and Posterior Segment Vascular Changes Due to Systemic Hypoxia Using Optical Coherence Tomography AngiographyNadav Levinger, Nir Erdinest, Ayman Abu Rmeileh, et al.
Investigative Ophthalmology & Visual Science|March 1, 2018
The Genetics of Usher Syndrome in the Israeli and Palestinian PopulationsAyat Khalaileh, Alaa Abu-Diab, Tamar Ben-Yosef, et al.
Journal of Clinical Medicine|March 27, 2025
Anterior Segment Characteristics and Quality of Life of Patients with Central Serous ChorioretinopathyHadas Ben-Eli, Tal Asher, Rivkah Lender, et al.
Molecular Vision|April 11, 2022
Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genesSamer Khateb, Aya Shemesh, Ashly Offenheim, et al.
Medicine|January 10, 2026
Evaluating a novel triangular suture technique for scleral support of dislocated intraocular lenses following cataract surgery: A retrospective cohort studyNir Erdinest, Michael Tabi, Or Shmueli, et al.
Translational Vision Science & Technology|March 1, 2023
Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in MiceAlaa Abu-Diab, Prakadeeswari Gopalakrishnan, Chen Matsevich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humansSamer Khateb, Björn Kowalewski, Nicola Bedoni, et al.
JAMA Ophthalmology|April 19, 2019
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6BSamer Khateb, Marco Nassisi, Kinga M Bujakowska, et al.
Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.
Pageof 7