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Jaime Levy

Showing results (161-170 of 168) with videos related to

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American Journal of Human Genetics|September 3, 2011
High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2Shikma Mordechai, Libe Gradstein, Annika Pasanen, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
International Journal of Ophthalmology|January 20, 2021
Endogenous fungal endophthalmitis: risk factors, clinical course, and visual outcome in 13 patientsJamel Corredores, Itzhak Hemo, Tareq Jaouni, et al.
American Journal of Medical Genetics. Part A|December 5, 2018
Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribeOhad Wormser, Libe Gradstein, Einat Kadar, 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.
BMJ Open Ophthalmology|May 21, 2020
Ophthalmology practice during the COVID-19 pandemicKhaled Safadi, Joshua M Kruger, Itay Chowers, 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.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 9, 2026
A deep learning model for automated identification of age-related macular degeneration atrophyOren Avram, Yahel Shwartz, Adi Green, et al.
Pageof 17

Showing results (161-170 of 168) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 168 results.
American Journal of Human Genetics|September 3, 2011
High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2Shikma Mordechai, Libe Gradstein, Annika Pasanen, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
International Journal of Ophthalmology|January 20, 2021
Endogenous fungal endophthalmitis: risk factors, clinical course, and visual outcome in 13 patientsJamel Corredores, Itzhak Hemo, Tareq Jaouni, et al.
American Journal of Medical Genetics. Part A|December 5, 2018
Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribeOhad Wormser, Libe Gradstein, Einat Kadar, 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.
BMJ Open Ophthalmology|May 21, 2020
Ophthalmology practice during the COVID-19 pandemicKhaled Safadi, Joshua M Kruger, Itay Chowers, 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.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 9, 2026
A deep learning model for automated identification of age-related macular degeneration atrophyOren Avram, Yahel Shwartz, Adi Green, et al.
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