Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Leila, El Matri"'
Autor:
Imen Habibi, Yosra Falfoul, Ahmed Turki, Asma Hassairi, Khaled El Matri, Ahmed Chebil, Daniel F. Schorderet, Leila El Matri
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Abstract We report the molecular basis of the largest Tunisian cohort with inherited retinal dystrophies (IRD) reported to date, identify disease-causing pathogenic variants and describe genotype–phenotype correlations. A subset of 26 families from
Externí odkaz:
https://doaj.org/article/265ffa3b52364d2eb4761790714b5dc7
Publikováno v:
Therapeutic Advances in Ophthalmology, Vol 13 (2021)
Purpose: To compare the therapeutic impact of combining intravitreal injections of bevacizumab (IVB) with micropulse laser (MPL) in central diffuse diabetic macular edema (DME) versus IVB monotherapy during 12 months follow-up. Methods: We conducted
Externí odkaz:
https://doaj.org/article/3c22f781650244aebf9464701c752a7f
Autor:
Imen Habibi, Yosra Falfoul, Hoai Viet Tran, Khaled El Matri, Ahmed Chebil, Leila El Matri, Daniel F. Schorderet
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Retinal dystrophies (RD) are a group of Mendelian disorders caused by rare genetic variations leading to blindness. A pathogenic variant may manifest in both dominant or recessive mode and clinical and genetic heterogeneity makes it difficult to esta
Externí odkaz:
https://doaj.org/article/9476dbf46f8c44d281df67af7e5ad36f
Autor:
Khaled El Matri, Yousra Falfoul, Imen Habibi, Ahmed Chebil, Daniel Schorderet, Leila El Matri
Publikováno v:
Genes, Vol 12, Iss 11, p 1795 (2021)
Purpose: We report the case of a neurologically asymptomatic young boy presenting with an unusual phenotype of CYP2U1 related macular dystrophy associating bilateral macular telangiectasia (MacTel) and fibrotic choroidal neovascularization (CNV), ass
Externí odkaz:
https://doaj.org/article/0bc2795b48574cab87878fb68be396ee
Case Report: Swept-source Optical Coherence Tomography and Angiography Findings in Lipemia Retinalis
Autor:
Rim, Bouraoui, Khaled, El Matri, Kaouther, Derouiche, Yousra, Falfoul, Chiraz, Amrouche, Ines, Hachicha, Emna, Othmani, Fatma, Mghaieth, Leila, El Matri
Publikováno v:
Optometry and Vision Science. 99:76-81
Lipemia retinalis is a very rare ocular manifestation of severe hypertriglyceridemia. It is usually symptomatic and regresses after normalization of triglycerides levels. Early recognition is important to prevent ocular and life-threatening complicat
Publikováno v:
Acta Ophthalmologica. 100
Autor:
Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
Publikováno v:
Genes, Vol 11, Iss 5, p 503 (2020)
The authors wish to make a correction to the published version of their paper [...]
Externí odkaz:
https://doaj.org/article/5b3c481095114b7eab33a2cb82f29d9e
Autor:
Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
Publikováno v:
Genes, Vol 10, Iss 12, p 953 (2019)
Mutations in BEST1 cause several phenotypes including autosomal dominant (AD) Best vitelliform macular dystrophy type 2 (BVMD), AD vitreo-retino-choroidopathy (ADVIRC), and retinitis pigmentosa-50 (RP50). A rare subtype of Bestrophinopathy exists wit
Externí odkaz:
https://doaj.org/article/f58892df8f7347548a239dd23931ebee
Autor:
Yousra Falfoul, Imen Habibi, Ahmed Turki, Ahmed Chebil, Asma Hassairi, Daniel F. Schorderet, Leila El Matri
Publikováno v:
Journal of Ophthalmology, Vol 2018 (2018)
To assess the progression of Stargardt (STGD) disease over nine years in two branches of a large consanguineous Tunisian family. Initially, different phenotypes were observed with clinical intra- and interfamilial variations. At presentation, four di
Externí odkaz:
https://doaj.org/article/0b25626c8c0b47d19a7f033948b28975
Autor:
Yousra Falfoul, Rim Bouraoui, Zied Chelly, Fatma Mghaieth, Ahmed Chebil, Leila El Matri, Khaled El Matri
Publikováno v:
European Journal of Ophthalmology. 33:NP72-NP77
Aim: To report an uncommon case of optic disc and multiple choroidal metastases secondary to breast cancer, assessed with swept source optical coherence tomography (SS-OCT), fluorescein (FA), and infracyanine (ICGA) angiographies. Methods: Observatio