Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Fedra Kort"'
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 5, Iss 2, Pp 127-129 (2010)
Purpose: To describe optical coherence tomography (OCT) findings in a patient with Berlin′s edema following blunt ocular trauma. Case Report: A 26-year-old man presented with acute loss of vision in his left eye following blunt trauma. He underwent
Externí odkaz:
https://doaj.org/article/128f9235cbcc4990a280a0123d67d230
Autor:
Leila El Matri, Rym Bouraoui, Ahmed Chebil, Fedra Kort, Mejda Bouladi, Rym Limaiem, Hana Landoulsi
Publikováno v:
Journal of Ophthalmology, Vol 2012 (2012)
Purpose. To evaluate functional and anatomic effects of intravitreal bevacizumab in patients with neovascular AMD and initial low visual acuity. Methods. Retrospective case series of 38 eyes with neovascular AMD and initial visual acuity of 20/200 or
Externí odkaz:
https://doaj.org/article/0d2f8bfca86d4ae18dc3ddf1288ee636
Autor:
Ahmed Chebil, Yousra Falfoul, L. El Matri, M. Kortli, A. Turki, A. Hassairi, Fedra Kort, H. Charfi
Publikováno v:
Journal Français d'Ophtalmologie. 40:666-675
Resume But Decrire l’apport de l’imagerie multimodale dans les differents stades de la maladie de Stargardt (STGD). Patients et methodes Quarante-six yeux de 23 patients atteints de STGD porteurs de mutations dans le gene ABCA4 ont ete inclus et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::811be4b91bb5cf88902b1aa7c43ed481
https://doi.org/10.1016/j.jfo.2017.05.008
https://doi.org/10.1016/j.jfo.2017.05.008
Publikováno v:
Ophthalmic Genetics. 38:494-497
Retinitis pigmentosa (RP), a hereditary retinal disorder causing degeneration of photoreceptors,1,2 displays large heterogeneity in terms of clinical manifestations, hereditary pattern, and causati...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00e0ed027a1781f14cc18d6bfbb5e3ba
https://doi.org/10.1080/13816810.2016.1275020
https://doi.org/10.1080/13816810.2016.1275020
Publikováno v:
Journal Français d'Ophtalmologie. 39:248-254
Resume Objectif Evaluer les resultats fonctionnels et anatomiques des injections intravitreennes de bevacizumab en monotherapie a 12 et a 24 mois dans les larges hemorragies sous maculaires compliquant la DMLA. Materiel et methodes Etude retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead8d6f1de988ce064e10381cd6cbb1d
https://doi.org/10.1016/j.jfo.2015.10.010
https://doi.org/10.1016/j.jfo.2015.10.010
Autor:
Leila El Matri, Rim Limaiem, Ahmed Chebil, Taieb Ben Abdallah, Fedra Kort, Imen Sfar, Imen Habibi, Yousr Gorgi, S. Ayed, Rim Bouraoui
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 234(4)
Purpose To explore the association between the polymorphism (S/F) p.R102G in the complement component 3 (C3) gene and age-related macular degeneration (AMD) in a Tunisian population. Methods The molecular study was performed by polymerase chain react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e8b5b5916afb2471ad49993ccdb9c3
https://pubmed.ncbi.nlm.nih.gov/28470643
https://pubmed.ncbi.nlm.nih.gov/28470643
Autor:
Imen, Habibi, Ahmed, Chebil, Yosra, Falfoul, Nathalie, Allaman-Pillet, Fedra, Kort, Daniel F, Schorderet, Leila El, Matri
Publikováno v:
Scientific Reports
Retinal dystrophies (RD) are a rare genetic disorder with high genetic heterogeneity. This study aimed at identifying disease-causing variants in fifteen consanguineous Tunisian families. Full ophthalmic examination was performed. Index patients were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03f8015cff81cac330be592116838af6
https://pubmed.ncbi.nlm.nih.gov/27874104
https://pubmed.ncbi.nlm.nih.gov/27874104
Publikováno v:
Journal Français d'Ophtalmologie. 37:296-302
Resume But Decrire un aspect particulier de la macula en SD-OCT au cours de l’achromatopsie congenitale complete. Materiels et methodes Six patients appartenant a trois familles tunisiennes consanguines presentant un nystagmus congenital et une amb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::613e37c3e1d57657425a288255a4ed9c
https://doi.org/10.1016/j.jfo.2013.12.008
https://doi.org/10.1016/j.jfo.2013.12.008
Publikováno v:
Journal Français d'Ophtalmologie. 36:687-692
Resume Introduction Le but de notre etude est de mesurer, au spectral-domain OCT (SD-OCT), l’epaisseur choroidienne foveolaire dans la myopie forte compliquee de neovaisseaux choroidiens et de la comparer par rapport a des yeux myopes forts sans co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f59c0a1d7d610f5ee97bff27c37738c0
https://doi.org/10.1016/j.jfo.2013.03.009
https://doi.org/10.1016/j.jfo.2013.03.009
Publikováno v:
Journal Français d'Ophtalmologie. 36:29-34
Resume But Comparer a long terme l’efficacite et l’innocuite des injections intravitreennes de bevacizumab versus la phototherapie dynamique a la verteporfine dans le traitement des neovaisseaux choroidiens (NVC) du myope fort. Methodes Nous avon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::688fd84047066887ed3e2b0e47bf9a0f
https://doi.org/10.1016/j.jfo.2012.03.015
https://doi.org/10.1016/j.jfo.2012.03.015