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Brain Structure & Function|February 15, 2015
Genetically induced impairment of retinal ganglion cells at the axonal level is linked to extrastriate cortical plasticityCatarina Mateus, Otília C d'Almeida, Aldina Reis, et al.Neuroimage|May 21, 2013
Long term cortical plasticity in visual retinotopic areas in humans with silent retinal ganglion cell lossOtília C d'Almeida, Catarina Mateus, Aldina Reis, et al.Journal of Glaucoma|February 3, 2015
A New Approach to Assess Early Progressive Loss Across Multiple Visual Channels In the Natural History of GlaucomaCatarina Mateus, Miguel Raimundo, Bárbara Oliveiros, et al.Journal of Vision|October 2, 2010
Asymmetry of visual sensory mechanisms: electrophysiological, structural, and psychophysical evidencesMaria Fátima Silva, Catarina Mateus, Aldina Reis, et al.Diabetes|June 21, 2014
Neuroretinal dysfunction with intact blood-retinal barrier and absent vasculopathy in type 1 diabetesAldina Reis, Catarina Mateus, Pedro Melo, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 7, 2012
Physiological evidence for impairment in autosomal dominant optic atrophy at the pre-ganglion levelAldina Reis, Catarina Mateus, Teresa Viegas, et al.Neural Plasticity|July 26, 2019
Enhanced Visual Attentional Modulation in Patients with Inherited Peripheral Retinal Degeneration in the Absence of Cortical DegenerationSónia Ferreira, Andreia Carvalho Pereira, Bruno Quendera, et al.Neuroimage. Clinical|January 25, 2017
Primary visual cortical remapping in patients with inherited peripheral retinal degenerationSónia Ferreira, Andreia Carvalho Pereira, Bruno Quendera, et al.Journal of Neurology|April 1, 2011
Independent patterns of damage to retinocortical pathways in multiple sclerosis without a previous episode of optic neuritisAldina Reis, Catarina Mateus, M Carmo Macário, et al.Investigative Ophthalmology & Visual Science|March 11, 2008
Evidence of widespread retinal dysfunction in patients with stargardt disease and morphologically unaffected carrier relativesSusana Maia-Lopes, Eduardo D Silva, Maria Fátima Silva, et al.Pageof 2