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The top documents of retinafoundation
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation
Standardized full-field electroretinography. Normal values and their variation with age
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene
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Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids
A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa*1
Method for deriving visual field boundaries from OCT scans of patients with retinitis pigmentosa
A randomized placebo-controlled clinical trial of docosahexaenoic acid (DHA) supplementation for X-linked retinitis pigmentosa
Transition Zones between Healthy and Diseased Retina in Choroideremia (CHM) and Stargardt Disease (STGD) as Compared to Retinitis Pigmentosa (RP)
A randomized placebo-controlled clinical trial of docosahexaenoic acid (DHA) supplementation for X-linked retinitis pigmentosa
The Transition Zone between Healthy and Diseased Retina in Patients with Retinitis Pigmentosa
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development
Genomic Rearrangements of the PRPF31 Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa
Loss of Caveolin-1 Impairs Retinal Function Due to Disturbance of Subretinal Microenvironment
Time-resolved FRET fluorescence spectroscopy of visible fluorescent protein pairs
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4
LCPUFA requirements for preterm infants: Neurophysiological Studies
Effects of ω-3 long-chain polyunsaturated fatty acid supplementation on retinal and cortical development in premature infants
Normative pediatric visual acuity using single surrounded HOTV optotypes on the Electronic Visual Acuity Tester following the Amblyopia Treatment Study protocol