z-logo
open-access-imgOpen Access
Evidence of Widespread Retinal Dysfunction in Patients with Stargardt Disease and Morphologically Unaffected Carrier Relatives
Author(s) -
Susana Maia-Lopes,
Eduardo Silva,
Maria Fa ́tima Silva,
Aldina Reis,
Pedro Faria,
Miguel CasteloBranco
Publication year - 2008
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.07-1051
Subject(s) - electroretinography , abca4 , parvocellular cell , stargardt disease , achromatic lens , ophthalmology , erg , medicine , biology , choroideremia , retinal , genetics , optometry , optics , phenotype , gene , physics , central nervous system
To characterize contrast sensitivity (CS) across the visual field for two achromatic spatial-temporal frequencies in 21 families with Stargardt disease (STGD) and to correlate psychophysical impairment with patterns of change in multifocal electroretinography (mfERG).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom