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Investigative Ophthalmology & Visual Science|August 2, 2017
C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel MutationsChristina Gerth-Kahlert, Amit Tiwari, James V M Hanson, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|May 29, 2024
The Fight Tumour Blindness Registry: Efficient capture of high-quality real-world data in uveal melanomaRoderick F O'Day, R Max Conway, Li-Anne Lim, et al.
Molecular Vision|June 17, 2008
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testingJohn Neidhardt, Esther Glaus, Birgit Lorenz, et al.
Eye (London, England)|September 21, 2024
Fight Retinal Blindness SPAIN. Report 3: clinical outcomes of vascular endothelial growth factor inhibitors in low vision eyes with neovascular age-related macular degeneration. A national database studyMartín Puzo, Pilar Calvo-Perez, Francisco Bartol-Puyal, et al.
Ophthalmology. Retina|November 4, 2023
Macular Neovascularization Type Influence on Anti-VEGF Intravitreal Therapy Outcomes in Age-Related Macular DegenerationJordi Izquierdo-Serra, Ruben Martin-Pinardel, Aina Moll-Udina, et al.
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