Visual acuity improvement in children with albinism beyond the first decade of life.

Autor: Claudia Yahalom, Ana Navarrete, Atara Juster, Ayan Galbinur, Anat Blumenfeld, Karen Hendler

Publikováno v: PLoS ONE, Vol 19, Iss 1, p e0296744 (2024)

PurposeTo determine if visual maturation continues beyond the first decade of life in children with albinism and whether this is related to albinism type, presence of nystagmus, eye muscle surgery or refractive errors.DesignCase series based on retro

Externí odkaz: https://doaj.org/article/93732124bc364f6085531f64909da445

Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in Israel

Autor: Karen Hendler, Rani Patal, Ibrahim Saadeh, Claudia Yahalom, Michal Macarov, Ron Braun, Anat Blumenfeld

Publikováno v: Eye. 36:2052-2056

BACKGROUND To assess the main causes leading to childhood visual impairment/blindness in a center for low vision in Israel and to analyze the literature on pediatric blinding diseases in developed countries. METHODS Retrospective study based on obser

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b21febefaefdfb23be566e053d423ae9
https://doi.org/10.1038/s41433-021-01743-3

Implementing enhanced education to improve the UCLA Preschool Vision Program

Autor: Fei Yu, Karen Hendler, Shiva Mehravaran, Ann Quan, Anne L. Coleman

Publikováno v: Journal of American Association for Pediatric Ophthalmology and Strabismus. 22:441-444

To examine whether educational pamphlets and videos for adults can increase follow-up rates for eye examinations among preschool children.The target population was 3- to 5-year-olds attending preschools within Los Angeles County and receiving service

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99c67f4d5e25e65f9f3e00873736ff0
https://doi.org/10.1016/j.jaapos.2018.07.346

Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease

Autor: Michal Macarov, Karen Hendler, Anat Blumenfeld, Claudia Yahalom, Orly Wussuki-Lior, Samer Khateb, Mordechai Shohat

Publikováno v: Graefe's Archive for Clinical and Experimental Ophthalmology. 256:2157-2164

Aniridia is a rare panocular disorder caused by mutations in the PAX6 gene and characterized mainly by iris hypoplasia. Here, we present six families with a history of low vision/blindness with a previously undiagnosed mild aniridia phenotype with mi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2fccc4f3bac13608bfc16e55cedb6c8
https://doi.org/10.1007/s00417-018-4119-1

TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

Autor: Karen Hendler, Claudia Yahalom, Isabelle Audo, Dror Sharon, Samer Khateb, Alaa AlTalbishi, Christina Zeitz, Prasanthi Namburi, Ruth Sheffer, Eyal Banin, Lina Zelinger

Publikováno v: Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-6 (2019)

Precise genetic and phenotypic characterization of congenital stationary night blindness (CSNB) patients is needed for future therapeutic interventions. The aim of this study was to estimate the prevalence of CSNB in our populations and to study clin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::366e3c7c5faeed44407c34e0bf0d8a2f
http://europepmc.org/articles/PMC6700182