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Meeting Abstract (3)
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Investigative Ophthalmology & Visual Science (5)

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ARVO Annual Meeting Abstract (3)
Genetics (1)
Retina (1)

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Eye Anatomy and Disorders (2)
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albinism (1)
electroretinography (1)
family (1)
genes (1)
genetics (1)
immunohistochemistry (1)
injections (1)
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ARVO Annual Meeting Abstract July 2018

Phase I/IIa Clinical Trial of Human Embryonic Stem Cell (hESC)-Derived Retinal Pigmented Epithelium (RPE, Opregen ® ) Transplantation in Advanced Dry Form Age-Related Macular Degeneration (AMD): Interim Results

Eyal Banin; Yitzchak Hemo; Tareq Jaouni; Devora Marks-Ohana; Maria Gurevich; Oscar Cuzzani; David S Boyer; Benjamin Reubinoff

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):77. doi:

ARVO Annual Meeting Abstract June 2017

Phase I/IIa clinical trial of human embryonic stem cell (hESC)-derived retinal pigmented epithelium (RPE, OpRegen ® ) transplantation in advanced dry form age-related macular degeneration (AMD): interim results

Eyal Banin; Yitzchak Hemo; Tareq Jaouni; Devora Marks-Ohana; Shelly Stika; Svetlana Zheleznykov; Alexey Obolensky; Maria Gurevich; Charles S/ Irving; Benjamin Reubinoff

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2320. doi:

Retina April 2017

Course of Sodium Iodate–Induced Retinal Degeneration in Albino and Pigmented Mice

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Guy Chowers; Matan Cohen; Devora Marks-Ohana; Shelly Stika; Ayala Eijzenberg; Eyal Banin; Alexey Obolensky
TAGS: albinism, iodates, mice, retinal degeneration, sodium, photoreceptors, injections, electroretinography, mice, inbred c57bl, immunohistochemistry
Invest. Ophthalmol. Vis. Sci.. 2017; 58(4):2239-2249. doi: https://doi.org/10.1167/iovs.16-21255

Includes: Supplemental Content

Genetics January 2015

Whole Exome Sequencing Reveals GUCY2D as a Major Gene Associated With Cone and Cone–Rod Dystrophy in Israel

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Csilla H. Lazar; Mousumi Mutsuddi; Adva Kimchi; Lina Zelinger; Liliana Mizrahi-Meissonnier; Devorah Marks-Ohana; Alexis Boleda; Rinki Ratnapriya; Dror Sharon; Anand Swaroop; Eyal Banin
TAGS: family, genes, israel, progressive cone-rod dystrophy, retinal cone, retinitis pigmentosa, whole exome sequencing, mutation, genetics, retinal diseases
Invest. Ophthalmol. Vis. Sci.. 2015; 56(1):420-430. doi: https://doi.org/10.1167/iovs.14-15647

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Phase I Gene Therapy Trial in Israeli Patients with Leber Congenital Amaurosis Caused by a Founder RPE65 Mutation: Safety and Efficacy Update with Up to Two Years of Follow-up

Eyal Banin; Alexey Obolensky; Yitzhak Hemo; Devora Marks-Ohana; Malka Sela; Esther Yamin; William Hauswirth; Samuel Jacobson; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):2709. doi:

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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