Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update

Documenta Ophthalmologica

Volumn 116, Issue 2, 2008, Pages 79-89

  Robson, Anthony G ^a,b   Michaelides, Michel ^a,b   Saihan, Zubin ^b   Bird, Alan C ^a,b   Webster, Andrew R ^a,b   Moore, Anthony T ^a,b   Fitzke, Fred W ^b   Holder, Graham E ^a  

^a MOORFIELDS EYE HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Autofluorescence imaging; Cone rod dystrophy; Electroretinography; Genotype phenotype correlation; Retinitis pigmentosa; Usher syndrome

Indexed keywords

GENE PRODUCT; GUANYLATE CYCLASE ACTIVATING PROTEIN 1; GUANYLATE CYCLASE ACTIVATOR; PROTEIN RIMS1; PROTEIN RPGR; UNCLASSIFIED DRUG; VOLTAGE GATED POTASSIUM CHANNEL;

AUTOFLUORESCENCE; CLINICAL ASSESSMENT; CLINICAL FEATURE; CONTROLLED STUDY; CORRELATION ANALYSIS; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; ELECTRORETINOGRAPHY; FUNCTIONAL ASSESSMENT; GENETIC SCREENING; HUMAN; LEBER CONGENITAL AMAUROSIS; MAJOR CLINICAL STUDY; NIGHT VISION; OPHTHALMOSCOPY; PHOTOPIC VISION; RETINA CONE; RETINA DYSTROPHY; RETINA FOVEA; RETINA ROD; RETINITIS PIGMENTOSA; RETINOSCHISIS; REVIEW; SENSITIVITY ANALYSIS; SENSORY SYSTEM ELECTROPHYSIOLOGY; USHER SYNDROME; VISUAL ACUITY; X CHROMOSOME LINKED DISORDER;

ELECTRORETINOGRAPHY; FLUORESCENCE; FOVEA CENTRALIS; FUNDUS OCULI; GENOTYPE; HUMANS; LIPOFUSCIN; PHENOTYPE; RETINITIS PIGMENTOSA; USHER SYNDROMES;

EID: 39649091008     PISSN: 00124486     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10633-007-9087-4     Document Type: Review

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