日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Epidemiology and Visual Outcome of Pediatric Ocular Trauma in a Major Tertiary Eye Center in Tunisia: A 6-Year Retrospective Study

突尼斯一家大型三级眼科中心儿童眼外伤的流行病学和视觉预后:一项为期6年的回顾性研究

Rmili, Mohamed Foued; Chebil, Ahmed; Limaiem, Rim; Chaker, Nibrass; Bouraoui, Rym; Falfoul, Yousra; El Matri, Leila

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

假显性遗传性视网膜营养不良的不同表型

Habibi, Imen; Falfoul, Yosra; Tran, Hoai Viet; El Matri, Khaled; Chebil, Ahmed; El Matri, Leila; Schorderet, Daniel F

Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography

采用包括OCT血管造影在内的多模态成像技术评估与CYP2U1致病变异相关的双侧黄斑毛细血管扩张性黄斑营养不良。

El Matri, Khaled; Falfoul, Yousra; Habibi, Imen; Chebil, Ahmed; Schorderet, Daniel; El Matri, Leila

Subthreshold micropulse laser adjuvant to bevacizumab versus bevacizumab monotherapy in treating diabetic macular edema: one- year- follow-up

亚阈值微脉冲激光辅助贝伐单抗治疗与贝伐单抗单药治疗糖尿病性黄斑水肿的比较:一年随访

El Matri, Leila; Chebil, Ahmed; El Matri, Khaled; Falfoul, Yousra; Chebbi, Zouheir

Multimodal imaging of bilateral ischemic retinal vasculopathy associated with Berger's IgA nephropathy: case report

双侧缺血性视网膜血管病变合并Berger IgA肾病的多模态影像学诊断:病例报告

El Matri, Khaled; Amoroso, Francesca; Zambrowski, Olivia; Miere, Alexandra; Souied, Eric H

Genetic spectrum of retinal dystrophies in Tunisia

突尼斯视网膜营养不良的遗传谱

Habibi, Imen; Falfoul, Yosra; Turki, Ahmed; Hassairi, Asma; El Matri, Khaled; Chebil, Ahmed; Schorderet, Daniel F; El Matri, Leila

Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10, 953

更正:Habibi I. 等人,“常染色体隐性遗传性雌激素病 (ARB) 的临床和遗传学发现”,《基因》,2019,10,953

Habibi, Imen; Falfoul, Yosra; Todorova, Margarita G; Wyrsch, Stefan; Vaclavik, Veronika; Helfenstein, Maria; Turki, Ahmed; El Matri, Khaled; El Matri, Leila; Schorderet, Daniel F

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)

常染色体隐性遗传性雌激素血症(ARB)的临床和遗传学发现

Habibi, Imen; Falfoul, Yosra; Todorova, Margarita G; Wyrsch, Stefan; Vaclavik, Veronika; Helfenstein, Maria; Turki, Ahmed; Matri, Khaled El; Matri, Leila El; Schorderet, Daniel F

Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

携带新的ABCA4突变的突尼斯近亲大家族中斯塔加特病的表型进展

Falfoul, Yousra; Habibi, Imen; Turki, Ahmed; Chebil, Ahmed; Hassairi, Asma; Schorderet, Daniel F; El Matri, Leila

Identifying mutations in Tunisian families with retinal dystrophy

识别突尼斯视网膜营养不良家族中的基因突变

Habibi, Imen; Chebil, Ahmed; Falfoul, Yosra; Allaman-Pillet, Nathalie; Kort, Fedra; Schorderet, Daniel F; El Matri, Leila