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Retina (Philadelphia, Pa.)|January 25, 2023
SYMPTOMATIC EARLY-ONSET X-LINKED RETINOSCHISIS: Clinical Presentation and OutcomesGwendoline Piquin, Youssef Abdelmassih, Gilles Martin, et al.
Frontiers in Medicine|August 22, 2022
Coats disease in female population: A comparison of clinical presentation and outcomesGwendoline Piquin, Thibaut Chapron, Youssef Abdelmassih, et al.
Ocular Immunology and Inflammation|September 7, 2016
Cataract Surgery with Primary Lens Implantation in Children with Chronic UveitisDamien Guindolet, Pascal Dureau, Céline Terrada, et al.
Acta Ophthalmologica|March 31, 2022
Congenital cataract surgery: long-term refractive outcomes of a new intraocular lens power correction formulaRomain Touzé, Pascal Dureau, Catherine Edelson, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 10, 2020
Outcome and risk factors of vitreoretinal surgery in pediatric patients with familial exudative vitreoretinopathySylvain El-Khoury, Ana Clement, Ismael Chehaibou, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Different HLA class IA region complotypes for HLA-A29.2 and -A29.1 antigens, identical in birdshot retinochoroidopathy patients or healthy individualsBéatrice Donvito, Dominique Monnet, Thierry Tabary, et al.
Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophyIsabelle Perrault, Sylvain Hanein, Xavier Zanlonghi, et al.
Plos One|January 12, 2013
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotypeIsabelle Perrault, Alejandro Estrada-Cuzcano, Irma Lopez, et al.
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