Retinal Imaging in Patients With Inherited Retinal Degenerations
Condition(s):Retinitis PigmentosaLast Updated:August 27, 2020Recruiting
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Condition(s):Retinitis PigmentosaLast Updated:August 27, 2020Recruiting
Condition(s):Eye Diseases Hereditary; Retinal Disease; Achromatopsia; Bardet-Biedl Syndrome; Bassen-Kornzweig Syndrome; Batten Disease; Best Disease; Choroidal Dystrophy; Choroideremia; Cone Dystrophy; Cone-Rod Dystrophy; Congenital Stationary Night Blindness; Enhanced S-Cone Syndrome; Fundus Albipunctatus; Goldmann-Favre Syndrome; Gyrate Atrophy; Juvenile Macular Degeneration; Kearns-Sayre Syndrome; Leber Congenital Amaurosis; Refsum Syndrome; Retinitis Pigmentosa; Retinitis Punctata Albescens; Retinoschisis; Rod-Cone Dystrophy; Rod Dystrophy; Rod Monochromacy; Stargardt Disease; Usher SyndromeLast Updated:December 13, 2018Recruiting
Condition(s):Retinitis Pigmentosa; Retinal DegenerationLast Updated:December 22, 2020Recruiting
Condition(s):Retinal Degeneration; Retinitis Pigmentosa; Eye Diseases, HereditaryLast Updated:February 21, 2021Not yet recruiting
Condition(s):Inherited Retinal Dystrophy Primarily Involving Sensory Retina; Inherited Retinal Dystrophy Primarily Involving Retinal Pigment EpitheliumLast Updated:October 18, 2019Recruiting
Condition(s):Inherited Retinal DystrophiesLast Updated:October 1, 2018Recruiting
Condition(s):Hereditary Retinal DystrophiesLast Updated:December 14, 2020Recruiting
Condition(s):Blindness; Leber Congenital Amaurosis 10; Vision Disorders; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease; Retinal DegenerationLast Updated:December 22, 2020Recruiting
Condition(s):Retinitis Pigmentosa Associated With CNGB1 MutationsLast Updated:March 5, 2021Recruiting
Condition(s):Vision Functional Brain Networks in Patients With Hereditary Retinal DystrophiesLast Updated:April 12, 2021Recruiting
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