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- Center for Hereditary Retinal Degenerations
- Contribute to State-of-the-Art Research
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Research
- Research Technique: Near-infrared excited Reduced-illuminance Autofluorescence Imaging
- RPGR and X-linked Retinitis Pigmentosa
- Optical coherence tomography (OCT) — Clinical
- RPE65-associated LCA
- ABCA4-associated Stargardt disease
- Interventions and Treatments: Clinical
- Interventions and Treatments: Pre-Clinical
- Research Technique: Pupilometry
- CEP290- and NPHP5-associated Leber congenital amaurosis
- Research Technique: Mathematical modeling
- Blue-cone monochromacy and achromatopsia
- RHO-associated autosomal dominant retinitis pigmentosa
- Age-related macular degeneration (AMD)
- Research technique: Microperimetry, fixation and nystagmus
- Research technique: Short-wavelength RAFI
- MYO7A-associated and other genetic forms of Usher syndrome
- NR2E3- and NRL-associated enhanced S-cone syndrome (ESCS)
- Dark-adaptation kinetics
- GUCY2D-LCA
- Other genetic forms of LCA
- Optical coherence tomography (OCT) - Animal Models
- Full-field Stimulus Testing (FST)
- functional MRI
- Orientation and Mobility
- Other inherited retinal degenerations
- Late-onset dominant retinal degenerations
- Electrophysiology - Clinical
- Electrophysiology - Preclinical
- Perimetry
- BEST1-associated retinopathies
- Refereed Journal Papers
- Recent Publications
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