Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Hadas Mechoulam"'
Autor:
David Landau, Radgonde Amer, Khaled Safadi, Joshua M. Kruger, Itay Chowers, Abraham Solomon, Hamzah Aweidah, Shahar Frenkel, Hadas Mechoulam, Irene Anteby, Hadas Ben Eli, Itay Lavy, Tarek Jaouni, Liran Tiosano, Gabriel Greifner, Shay Ofir, Tamar Levi Vineberg, Jaime Levy
Publikováno v:
BMJ Open Ophthalmology, Vol 5, Iss 1 (2020)
Objective To present an established practice protocol for safe and effective hospital-setting ophthalmic practice during the coronavirus disease 2019 (COVID-19) pandemic.Methods and Analysis Literature was reviewed to identify articles relevant to CO
Externí odkaz:
https://doaj.org/article/77edc4ff6bf84a7193c1f8001867dfa3
Publikováno v:
Ocular Immunology and Inflammation. 31:455-461
To report two cases masquerading as TORCH but eventually diagnosed with Enhanced S-cone Syndrome (ESCS).Descriptive case report.Ocular manifestations in ESCS can be reminiscent to TORCH. CNV may develop with an incidence of 15%. We report the younges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::405be95728b5dd56dbdde472ae88bf79
https://doi.org/10.1080/09273948.2022.2028290
https://doi.org/10.1080/09273948.2022.2028290
Publikováno v:
Journal of Visual Impairment & Blindness. 116:61-69
Introduction Pediatric cataract is still a major cause for childhood visual impairment. The goal of our study was to analyze the prevalence of children with impaired vision (6/15 or worse) after surgery for bilateral cataract, to evaluate factors ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19b7238817f0afeead2d775fa5bd2047
https://doi.org/10.1177/0145482x211073588
https://doi.org/10.1177/0145482x211073588
Autor:
Mor Hanany, Nadav Levinger, Karen Hendler, Yoav Parag, Claudia Yahalom, Dror Sharon, Vardiella Meiner, Adva Kimchi, Eyal Banin, Hadas Mechoulam, Michal Macarov
Publikováno v:
European Journal of Ophthalmology. 31:3349-3354
Purpose: Knobloch syndrome is a rare, recessively inherited disorder classically characterized by high myopia, retinal detachment, and occipital encephalocele. Our aim is to report the clinical and genetic findings of four Israeli children affected b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02f8879706af5621f03b707c654e9ca8
https://doi.org/10.1177/1120672120977343
https://doi.org/10.1177/1120672120977343
Autor:
Vardiella Meiner, Dror Sharon, Christina Zeitz, Hagar Mor-Shaked, Hadas Mechoulam, Claudia Yahalom, Adva Kimchi, Eyal Banin, Isabelle Audo, Shira Silverstein, Michal Macarov, Anat Blumenfeld
Publikováno v:
Ophthalmic Genetics. 40:443-448
Background: Mutations in CACNA1F have been mainly associated with X-linked incomplete congenital stationary night blindness (icCSNB). Variable phenotypic expression in females was reported in some families. We report here three non-related Ashkenazi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::382ce1e499ae38a67b9b06fd9d08913c
https://doi.org/10.1080/13816810.2019.1681008
https://doi.org/10.1080/13816810.2019.1681008
Autor:
Nadav, Levinger, Karen, Hendler, Eyal, Banin, Mor, Hanany, Adva, Kimchi, Hadas, Mechoulam, Vardiella, Meiner, Yoav, Parag, Dror, Sharon, Michal, Macarov, Claudia, Yahalom
Publikováno v:
European journal of ophthalmology. 31(6)
Knobloch syndrome is a rare, recessively inherited disorder classically characterized by high myopia, retinal detachment, and occipital encephalocele. Our aim is to report the clinical and genetic findings of four Israeli children affected by Knobloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d3cb54aa1a2069d22681f3233fd066b8
https://pubmed.ncbi.nlm.nih.gov/33238767
https://pubmed.ncbi.nlm.nih.gov/33238767
Autor:
Adva, Kimchi, Vardiella, Meiner, Shira, Silverstein, Michal, Macarov, Hagar, Mor-Shaked, Anat, Blumenfeld, Isabelle, Audo, Christina, Zeitz, Hadas, Mechoulam, Eyal, Banin, Dror, Sharon, Claudia, Yahalom
Publikováno v:
Ophthalmic genetics. 40(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcf39876831fab19f8765e5ee7f14e99
https://pubmed.ncbi.nlm.nih.gov/31651202
https://pubmed.ncbi.nlm.nih.gov/31651202
Autor:
Michal Gur, Orly Elpeleg, Ephrat Levy-Lahad, Hadas Mechoulam, Tamar Harel, Vardiella Meiner, Smadar Horowitz-Cederboim, Muhannad Daana
Publikováno v:
Eur J Hum Genet
The transforming growth factor-beta (TGFβ) signaling pathway is essential for palatogenesis and retinal development. Glycoprotein A repetitions predominant (GARP), encoded by LRRC32, is a TGFβ cell surface receptor that has been studied primarily i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::889b9cd48e3cf65a8b95b00810b129b5
https://europepmc.org/articles/PMC6777458/
https://europepmc.org/articles/PMC6777458/
Autor:
Irene Anteby, Tamar Levi Vineberg, Radgonde Amer, Hamzah Aweidah, Shay Ofir, Shahar Frenkel, Liran Tiosano, Jaime Levy, Itay Chowers, Hadas Ben Eli, David Landau, Itay Lavy, Abraham Solomon, Hadas Mechoulam, Khaled Safadi, Gabriel Greifner, Joshua M. Kruger, Tarek Jaouni
Publikováno v:
BMJ Open Ophthalmology
BMJ Open Ophthalmology, Vol 5, Iss 1 (2020)
BMJ Open Ophthalmology, Vol 5, Iss 1 (2020)
ObjectiveTo present an established practice protocol for safe and effective hospital-setting ophthalmic practice during the coronavirus disease 2019 (COVID-19) pandemic.Methods and AnalysisLiterature was reviewed to identify articles relevant to COVI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d0ac669964a8db94f82cf27c59221dc
https://doi.org/10.1136/bmjophth-2020-000487
https://doi.org/10.1136/bmjophth-2020-000487
Autor:
Abraham Zlotogorski, Hadas Mechoulam, Yuval Ramot, Rula Siam, Sofia Babay, Vered Molho-Pessach
Publikováno v:
Ophthalmic Genetics. 36:365-368
H syndrome is an autosomal recessive histiocytosis with multisystemic involvement caused by mutations in the SLC29A3 gene. The term H syndrome was coined to denote the major clinical findings which include hyperpigmentation, hypertrichosis, hearing l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b3db1ff0b2001ac3e106b77b459532
https://doi.org/10.3109/13816810.2014.886272
https://doi.org/10.3109/13816810.2014.886272