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ARVO Annual Meeting Abstract June 2020

Whole exome sequencing identified novel homozygous ALMS1 mutations in a Tunisian family with Alström syndrome

Imen Habibi; Yousra Falfoul; Ahmed Turki; Leila El Matri; Daniel F Schorderet

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2403.

ARVO Annual Meeting Abstract June 2020

Report of a Tunisian family with phenotypic variability linked to BEST 1 mutation

Leila El Matri; Yousra Falfoul; Habibi Imen; Khaled ElMatri; AHMED chebil; Asma Hassairi; Daniel F Schorderet

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2425.

ARVO Annual Meeting Abstract July 2019

Report of five families with autosomal recessive Bestrophinopathies (ARB)

Habibi Imen; Yosra Falfoul; Margarita G. Todorova; Stefan Wyrsch; Daniel F Schorderet; Leila El Matri

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):398.

ARVO Annual Meeting Abstract June 2017

Novel RPGRIP1 mutation in Leber congenital amaurosis patients

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

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3239.

ARVO Annual Meeting Abstract June 2017

Consanguineous Tunisian Family With Enhanced-S-cone Syndrome

youssr louati; Veronika Vaclavik; Daniel F Schorderet; Imen Habibi

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4685.

ARVO Annual Meeting Abstract April 2014

Effect of Risk Alleles in CFH, C3, and VEGFA on the Response to Intravitreal Bevacizumab in Tunisian patients with neovascular AMD

Habibi Imen; Fedra Kort; Imen Sfar; Ahmed Chebil; Rim Bouraoui; Taïeb Ben Abdallah; Leila El Matri; Yousr Gorgi

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):77.

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