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Investigative Ophthalmology & Visual Science|May 21, 2010
Glucose-6-phosphate-dehydrogenase deficiency as a risk factor for pterygiumEnrico Peiretti, Antonella Mandas, Pierluigi Cocco, et al.
Plos One|November 30, 2018
Optical coherence tomography is a useful tool in the differentiation between true edema and pseudoedema of the optic discArturo Carta, Paolo Mora, Raffaella Aldigeri, et al.
Frontiers in Aging Neuroscience|November 27, 2014
Cognitive Impairment and Age-Related Vision Disorders: Their Possible Relationship and the Evaluation of the Use of Aspirin and Statins in a 65 Years-and-Over Sardinian PopulationAntonella Mandas, Rosa Maria Mereu, Olga Catte, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patientsFrancesca Simonelli, Carmela Ziviello, Francesco Testa, et al.
Acta Ophthalmologica|December 8, 2015
Health-related quality of life in patients with primary open-angle glaucoma. An Italian multicentre observational studyIrene Floriani, Luciano Quaranta, Eliana Rulli, et al.
European Journal of Ophthalmology|August 17, 2021
Non-infectious uveitis burden on quality of life and work impairment assessed through different psychometric questionnairesLuca Cimino, Piergiorgio Neri, Elisabetta Miserocchi, et al.
Investigative Ophthalmology & Visual Science|September 24, 2010
Molecular and clinical characterization of albinism in a large cohort of Italian patientsAnnagiusi Gargiulo, Francesco Testa, Settimio Rossi, et al.
Investigative Ophthalmology & Visual Science|March 30, 2002
BIGH3 mutation spectrum in corneal dystrophiesFrancis L Munier, Beatrice E Frueh, Philippe Othenin-Girard, et al.
Plos One|September 19, 2014
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 lociClaire L Simpson, Robert Wojciechowski, Konrad Oexle, et al.
Human Molecular Genetics|March 12, 2013
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorDwight Stambolian, Robert Wojciechowski, Konrad Oexle, et al.
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