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Meeting Abstract (9)
Journal Articles (1)

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Investigative Ophthalmology & Visual Science (10)

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ARVO Annual Meeting Abstract (9)
Retina (1)

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Eye Anatomy and Disorders (1)
Genetics (1)
Imaging (1)
Retina (1)
Retinal Imaging (1)

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electroretinography (1)
genes (1)
heterozygote (1)
homozygote (1)
mutation (1)
retinal cone (1)
syndrome (1)

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ARVO Annual Meeting Abstract July 2018

Carrier Frequency Analysis of Mutations Causing Recessive Inherited Retinal Diseases in the Israeli Population

Dror Sharon; Gilad Allon; Adva Kimchi; Anat Blumenfeld; Hadas Newman; Eran Pras; Libe Gradstein; Eyal Banin; Tamar Ben-Yosef; Mor Hanany

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3494. doi:

ARVO Annual Meeting Abstract June 2017

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects

Adva Kimchi; Samer Khateb; Rong Wen; Ziqiang Guan; Eran Pras; Shoshi Kurtzman; Samuel G Jacobson; Hadas Newman; Tamar Ben-Yosef; Eyal Banin; Dror Sharon

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):570. doi:

ARVO Annual Meeting Abstract June 2017

The Israeli Inherited Retinal Diseases Consortium (IIRDC): Mapping Inherited Retinal Diseases in the Israeli Population

Dror Sharon; Tamar Ben-Yosef; Nitza Goldenberg-Cohen; Libe Gradstein; Eran Pras; Anan Abbasi; Noam Shomron; Eedy Mezer; Miriam Ehrenberg; Shiri Zayit-Soudry; Hadas Newman; Rina Leibu; Ygal Rotenstreich; Haim Levy; Eyal Banin; Ido Perlman

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1238. doi:

ARVO Annual Meeting Abstract June 2017

Retinitis pigmentosa-associated cystoid macular edema has inflammatory optical density characteristics

Tomer Batash; Hadas Newman; Adiel Barak; Shiri Zayit-Soudry; Eran Pras; Eyal Banin; Michael Politis; Anat Loewenstein; Meira Neudorfer

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3236. doi:

Retina October 2016

Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone Syndrome

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Hadas Newman; Sergiu C. Blumen; Itzhak Braverman; Rana Hanna; Beatrice Tiosano; Ido Perlman; Tamar Ben-Yosef
TAGS: electroretinography, genes, homozygote, mutation, retinal cone, syndrome, heterozygote
Invest. Ophthalmol. Vis. Sci.. 2016; 57(13):5361-5371. doi: https://doi.org/10.1167/iovs.16-19505

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

A combination of oculopharyngeal muscular dystrophy and a variant of enhanced S-cone syndrome in Bukharan Jews due to linked mutations in PABPN1 and NRL

Tamar Ben-Yosef; Hadas Newman; Itzhak Braverman; Sergiu Blumen; Rana Hanna; Beatrice Tiosano; Ido Perlman

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3165. doi:

ARVO Annual Meeting Abstract June 2015

An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy

Tamar Ben-Yosef; Osnat Eidinger; Rina Leibu; Hadas Newman; Leah Rizel; Ido Perlman

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2898. doi:

ARVO Annual Meeting Abstract March 2012

Optical Coherence Tomography in Preeclamptic Women

Meira Neudorfer; Oriel Spierer; maya Ben-Amitai Hertman; Hadas Newman; Sarit Barak; Adiel Barak; Isca Asher-Landsberg

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):2679. doi:

ARVO Annual Meeting Abstract April 2011

Subfoveal Choroidal Melanoma: Pretreatment Characteristics and Response To Plaque Radiation Therapy

Kimberly J. Chin; Hadas Newman; Paul T. Finger

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3282. doi:

ARVO Annual Meeting Abstract April 2011

Involvement Of CD24 In Angiogenesis In A Mouse Model Of Oxygen-induced Retinopathy

Adiel Barak; Shiran Shapira; Sarah Kraus; Mordechai Rosner; Sarah Pri-Chen; Oriel Spierer; Anat Lowenstein; Nadir Arber; Hadas Newman

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3168. 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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