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Eedy Mezer

Showing results (61-70 of 67) with videos related to

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JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Harefuah|February 20, 2019
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]Dror Sharon, Tamar Ben-Yosef, Eran Pras, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 27, 2022
The impact of the first peak of the COVID-19 pandemic on childhood myopia control practice patterns among ophthalmologists-an international pediatric ophthalmology and strabismus council global perspectiveJonathan Kfir, Tamara Wygnanski-Jaffe, Sonal Farzavandi, et al.
Genes|July 29, 2025
Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical DiagnosisSofia Kulyamzin, Rina Leibu, Hadas Newman, et al.
BMC Medical Genetics|May 2, 2006
Eight previously unidentified mutations found in the OA1 ocular albinism geneHélène Mayeur, Olivier Roche, Christelle Vêtu, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
JAMA Ophthalmology|May 16, 2024
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli PopulationSapir Shalom, Tamar Ben-Yosef, Ifat Sher, et al.
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Showing results (61-70 of 67) with videos related to

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Pageof 7
You have reached the last page of results.This site can display upto 67 results.
JAMA Ophthalmology|July 17, 2025
Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal DegenerationManar Salameh, Ghadeer Abu Tair, Samira Mousa, et al.
Harefuah|February 20, 2019
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]Dror Sharon, Tamar Ben-Yosef, Eran Pras, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 27, 2022
The impact of the first peak of the COVID-19 pandemic on childhood myopia control practice patterns among ophthalmologists-an international pediatric ophthalmology and strabismus council global perspectiveJonathan Kfir, Tamara Wygnanski-Jaffe, Sonal Farzavandi, et al.
Genes|July 29, 2025
Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical DiagnosisSofia Kulyamzin, Rina Leibu, Hadas Newman, et al.
BMC Medical Genetics|May 2, 2006
Eight previously unidentified mutations found in the OA1 ocular albinism geneHélène Mayeur, Olivier Roche, Christelle Vêtu, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
JAMA Ophthalmology|May 16, 2024
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli PopulationSapir Shalom, Tamar Ben-Yosef, Ifat Sher, et al.
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