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Human Genetics|June 16, 2009
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1Mounira Hmani-Aifa, Salma Ben Salem, Zeineb Benzina, et al.Investigative Ophthalmology & Visual Science|January 22, 2015
Cyclocoagulation of the ciliary bodies by high-intensity focused ultrasound: a 12-month multicenter studyPhilippe Denis, Florent Aptel, Jean-François Rouland, et al.Gene|July 4, 2013
Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 geneMariem Ben Said, Ebtissem Chouchène, Salma Ben Salem, et al.European Journal of Ophthalmology|June 26, 2012
Prevalence and risk factors for ocular surface disease among patients treated over the long term for glaucoma or ocular hypertensionChristophe Baudouin, Jean-Paul Renard, Jean-Philippe Nordmann, et al.International Ophthalmology|October 3, 2019
Increased choroidal thickness in primary angle closure measured by swept-source optical coherence tomography in Caucasian populationDiem-Trang Nguyen, Audrey Giocanti-Aurégan, Nassima Benhatchi, et al.Nature Genetics|May 3, 2011
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and miceK Saidas Nair, Mounira Hmani-Aifa, Zain Ali, et al.Ophthalmology. Glaucoma|July 30, 2021
Safety and Effectiveness of the PRESERFLO® MicroShunt in Primary Open-Angle Glaucoma: Results from a 2-Year Multicenter StudyHenny J M Beckers, Florent Aptel, Carroll A B Webers, et al.Pageof 3