RETeval: Evaluation of light- and dark-adapted ERGs using a mydriasis-free, portable system: clinical classifications and normative data
The purpose of this study was to determine the intra-visit reliability and diagnostic capability of a handheld, mydriasisfree ERG, RETeval (LKC Technologies, Gaithersburg, MD, USA), in comparison with the standard clinical ff-ERG by measuring responses recommended by the International Society for Clinical Electrophysiology of Vision (ISCEV).
