Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Edward Averbukh"'
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 3, Pp 793-797 (2022)
This report describes a case of central serous chorioretinopathy (CSCR) occurring following cessation of terbinafine treatment. A 51-year-old man presented for a routine ophthalmic examination. He was treated with oral terbinafine for onychomycosis u
Externí odkaz:
https://doaj.org/article/323017102857428f813c0b6c550d5def
Autor:
Jamel Corredores, Itzhak Hemo, Tareq Jaouni, Zohar Habot-Wilner, Michal Kramer, Shiri Shulman, Haneen Jabaly-Habib, Ala'a Al-Talbishi, Michael Halpert, Edward Averbukh, Jaime Levy, Iris Deitch-Harel, Radgonde Amer
Publikováno v:
International Journal of Ophthalmology, Vol 14, Iss 1, Pp 97-105 (2021)
AIM: To analyze the risk factors, ophthalmological features, treatment modalities and their effect on the visual outcome in patients with endogenous fungal endophthalmitis (EFE). METHODS: Data retrieved from the medical files included age at presenta
Externí odkaz:
https://doaj.org/article/d20a548b49754ff5a540bf47d51ee858
Publikováno v:
Current Eye Research. 46:539-545
To evaluate the anatomical correlation between fellow eyes for bilateral second-line anti-VEGF treatment in eyes with bilateral diabetic macular edema (DME) with incomplete response to first-line bevacizumab therapy.Seventy-four eyes (The mean±SD ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dae54244f4aaf0a57f8f72b03c19050d
https://doi.org/10.1080/02713683.2020.1812085
https://doi.org/10.1080/02713683.2020.1812085
Autor:
Esther Yamin, Elisha Gootwine, Alexey Obolensky, Eyal Banin, Raaya Ezra-Elia, Edward Averbukh, Ron Ofri, William W. Hauswirth, Hay Dvir, Maya Ross, Hen Honig, Alexander Rosov
Publikováno v:
Human Gene Therapy. 31:719-729
Gene augmentation therapy based on subretinal delivery of adeno-associated viral (AAV) vectors is proving to be highly efficient in treating several inherited retinal degenerations. However, due to potential complications and drawbacks posed by subre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818d5537ca37d9c1e347b78eb1fc0401
https://doi.org/10.1089/hum.2020.023
https://doi.org/10.1089/hum.2020.023
Publikováno v:
J Neurosci
The ability of the adult human brain to develop function following correction of congenital deafferentation is controversial. Specifically, cases of recovery from congenital visual deficits are rare. CNGA3-achromatopsia is a congenital hereditary dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4eb5743cfc978b721b51e599248b41a
https://europepmc.org/articles/PMC8412991/
https://europepmc.org/articles/PMC8412991/
Autor:
Tareq Jaouni, Tali Bdolah-Abram, Liran Tiosano, Itay Chowers, Eyal Banin, Shayan Yousefi, Edward Averbukh
Purpose: To evaluate the thickness of the ellipsoid zone (EZ) layer and its correlation with visual acuity and the disease stage in eyes with Adult-onset foveomacular vitelliform dystrophy (AFVD).Materials and Methods: Ninety-two eyes of 57 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::929410756572d1654d7a3aa0c8ce0cc0
https://doi.org/10.21203/rs.3.rs-603729/v1
https://doi.org/10.21203/rs.3.rs-603729/v1
Autor:
A. Rosov, Deniz Dalkara, H. Honig, Ron Ofri, Esther Yamin, Eyal Banin, Edward Averbukh, Maya Ross, Melissa Desrosiers, E. Gootwine, Alexey Obolensky, Raaya Ezra-Elia, H. Dvir
Publikováno v:
Gene therapy. 29(10-11)
Sheep carrying a mutated CNGA3 gene exhibit diminished cone function and provide a naturally occurring large animal model of achromatopsia. Subretinal injection of a vector carrying the CNGA3 transgene resulted in long-term recovery of cone function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2d2ce007dafa1b99819a8c378009c6a
https://pubmed.ncbi.nlm.nih.gov/34853444
https://pubmed.ncbi.nlm.nih.gov/34853444
Autor:
Edward Averbukh, William W. Hauswirth, Hen Honig, Maya Ross, Alexander Rosov, Eyal Banin, Alexey Obolensky, Raaya Ezra-Elia, Elisha Gootwine, Ron Ofri
Publikováno v:
Human Gene Therapy. 29:1376-1386
Achromatopsia causes severely reduced visual acuity, photoaversion, and inability to discern colors due to cone photoreceptor dysfunction. In 2010, we reported on day-blindness in sheep caused by a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f55bf8af99b1522ffd7bf8b0f3d1dd09
https://doi.org/10.1089/hum.2018.076
https://doi.org/10.1089/hum.2018.076
Autor:
Mazen Abu-Siam, Elisha Gootwine, Alexander Rosov, Oren Pe'er, Liat Gantz, Hay Dvir, Edward Averbukh, Ron Ofri, Hen Honig, Maya Ross, Eyal Banin, Dikla Arad, Alexey Obolensky, Itzhak Aizenberg
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports
Scientific Reports
Achromatopsia is an inherited retinal disease characterized by loss of cone photoreceptor function. Day blind CNGA3 mutant Improved Awassi sheep provide a large animal model for achromatopsia. This study measured refractive error and axial length par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::534b597204919319ac9539cd7c427da9
https://doi.org/10.1038/s41598-020-76205-z
https://doi.org/10.1038/s41598-020-76205-z
Autor:
Mor Ben-Yair, Scott Ehrenberg, Shiri Zayit-Soudry, Diego Almeida, Laura Derman, Yoreh Barak, Tareq Jaouni, Edward Averbukh, Shiran Almus, Michael Mimouni
Publikováno v:
Retina (Philadelphia, Pa.). 40(6)
PURPOSE To identify factors associated with persistent subretinal fluid (SRF) after small-gauge pars plana vitrectomy for primary rhegmatogenous retinal detachment. METHODS This retrospective study included patients from 2 tertiary centers who underw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7e5608f976741023c64a5f55aa5d99
https://pubmed.ncbi.nlm.nih.gov/31241497
https://pubmed.ncbi.nlm.nih.gov/31241497