A. Merdassi

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene

Ahmed Rebai, D. Schorderet, S. Abdelhak, 2011, Journal of Human Genetics.

Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, Tunisia.

S. Abdelhak, A. Merdassi, K. Derouiche, 2014, Journal francais d'ophtalmologie.

[Therapeutic penetrating keratoplasty in herpes infected eye].

A. Merdassi, L. el Matri, R. Limaiem, 2009, Bulletin de la Societe belge d'ophtalmologie.

[Severe microbial keratitis: report of 100 cases].

A. Merdassi, L. el Matri, R. Limaiem, 2007, Journal francais d'ophtalmologie.

[Ophthalmologic manifestations of congenital rubella].

A. Merdassi, L. Matri, Y. Falfoul, 2011, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Clinical and angiographic characteristics of Bietti's corneoretinal dystrophy: a case study of an 8-year-old girl].

A. Merdassi, L. el Matri, N. Chaker, 2007, Journal francais d'ophtalmologie.

Intravitreal bevacizumab versus photodynamic therapy for myopic choroidal neovascularization in a North-African population

A. Merdassi, L. el Matri, A. Chebil, 2011, Graefe's Archive for Clinical and Experimental Ophthalmology.

Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports

S. Abdelhak, M. Mokni, F. Ouechtati, 2010, Journal of Medical Case Reports.

reportCoexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family : two case reports

S. Abdelhak, M. Mokni, F. Ouechtati, 2015 .