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Itay Chowers

Showing results (101-110 of 135) with videos related to

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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.
Retina (Philadelphia, Pa.)|February 20, 2010
Bevacizumab for choroidal neovascularization related to inflammatory diseasesMichal Kramer, Ruth Axer-Siegel, Tareq Jaouni, et al.
Human Molecular Genetics|October 2, 2003
Gene expression variation in the adult human retinaItay Chowers, Dongmei Liu, Ronald H Farkas, et al.
Eye (London, England)|May 1, 2020
A 12-month prospective study to evaluate the efficacy of using the treat-and-extend regimen with intravitreal aflibercept as a Second-Line Treatment for Diabetic Macular Oedema (the TADI Study)Liran Tiosano, Rita Ehrlich, Yoreh Barak, 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.
European Journal of Ophthalmology|June 20, 2018
Diabetic macular edema treated with ranibizumab following bevacizumab failure in Israel (DERBI study)Rita Ehrlich, Russell Pokroy, Ori Segal, et al.
Investigative Ophthalmology & Visual Science|November 25, 2024
Adult Onset Foveomacular Vitelliform Dystrophy Shows Genetic Overlap With Age-Related Macular DegenerationShlomit Jaskoll, Adi Kramer, Sarah Elbaz-Hayoun, et al.
Investigative Ophthalmology & Visual Science|February 28, 2020
Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMDMichelle Grunin, Gala Beykin, Elior Rahmani, et al.
American Journal of Human Genetics|August 14, 2010
Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosaDikla Bandah-Rozenfeld, Liliana Mizrahi-Meissonnier, Chen Farhy, et al.
Investigative Ophthalmology & Visual Science|August 27, 2003
Identification of novel genes preferentially expressed in the retina using a custom human retina cDNA microarrayItay Chowers, Tushara L Gunatilaka, Ronald H Farkas, et al.
Pageof 14

Showing results (101-110 of 135) with videos related to

Sort By:
Pageof 14
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.
Retina (Philadelphia, Pa.)|February 20, 2010
Bevacizumab for choroidal neovascularization related to inflammatory diseasesMichal Kramer, Ruth Axer-Siegel, Tareq Jaouni, et al.
Human Molecular Genetics|October 2, 2003
Gene expression variation in the adult human retinaItay Chowers, Dongmei Liu, Ronald H Farkas, et al.
Eye (London, England)|May 1, 2020
A 12-month prospective study to evaluate the efficacy of using the treat-and-extend regimen with intravitreal aflibercept as a Second-Line Treatment for Diabetic Macular Oedema (the TADI Study)Liran Tiosano, Rita Ehrlich, Yoreh Barak, 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.
European Journal of Ophthalmology|June 20, 2018
Diabetic macular edema treated with ranibizumab following bevacizumab failure in Israel (DERBI study)Rita Ehrlich, Russell Pokroy, Ori Segal, et al.
Investigative Ophthalmology & Visual Science|November 25, 2024
Adult Onset Foveomacular Vitelliform Dystrophy Shows Genetic Overlap With Age-Related Macular DegenerationShlomit Jaskoll, Adi Kramer, Sarah Elbaz-Hayoun, et al.
Investigative Ophthalmology & Visual Science|February 28, 2020
Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMDMichelle Grunin, Gala Beykin, Elior Rahmani, et al.
American Journal of Human Genetics|August 14, 2010
Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosaDikla Bandah-Rozenfeld, Liliana Mizrahi-Meissonnier, Chen Farhy, et al.
Investigative Ophthalmology & Visual Science|August 27, 2003
Identification of novel genes preferentially expressed in the retina using a custom human retina cDNA microarrayItay Chowers, Tushara L Gunatilaka, Ronald H Farkas, et al.
Pageof 14