Skip to main navigation
Skip to search
Skip to main content
The Rotterdam Eye Hospital and Rotterdam Ophthalmic Institute Home
English
Nederlands
Search content at The Rotterdam Eye Hospital and Rotterdam Ophthalmic Institute
Home
Research output
Profiles
Activities
Press/Media
Research units
Clinical course of cone dystrophy caused by mutations in the RPGR gene
Alberta A H J Thiadens
, Gyan G Soerjoesing
, Ralph J Florijn
, A G Tjiam
, Anneke I den Hollander
,
L Ingeborgh van den Born
, Frans C Riemslag
, Arthur A B Bergen
, Caroline C W Klaver
Medical retina and Uveitis
Research output
:
Contribution to journal
›
Article
›
Research
›
peer-review
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Clinical course of cone dystrophy caused by mutations in the RPGR gene'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Clinical Course
100%
Cone Dystrophy
100%
RPGR Gene
100%
Female Carrier
75%
Visual Acuity
50%
ORF15
50%
Spectral Domain Optical Coherence Tomography (SD-OCT)
25%
Visual Outcome
25%
Medical Records
25%
Late-onset
25%
Fundus Autofluorescence
25%
Visual Loss
25%
Survival Analysis
25%
Legally Blind
25%
Electroretinography
25%
Photopic
25%
Fundus Photography
25%
Full-field Electroretinography
25%
Visual Prognosis
25%
All-affected
25%
Frameshift mutation
25%
Cumulative Risk
25%
Dark Adaptation
25%
X-linked
25%
Ophthalmoscopy
25%
Color Vision Testing
25%
Rod Photoreceptor
25%
Goldmann Perimetry
25%
Direct Sequencing
25%
Scotopic Response
25%
Small Families
25%
Ocular Involvement
25%
Non-carriers
25%
Kaplan-Meier
25%
Product-limit
25%
Terminal Region
25%
3-terminal
25%
Medicine and Dentistry
Disease Course
100%
Cone Dystrophy
100%
Visual Acuity
66%
Electroretinography
66%
Dark Adaptation
66%
Optical Coherence Tomography
33%
Disease
33%
Medical Record
33%
Fundus Photography
33%
Autofluorescence
33%
Photoreceptor
33%
Visual Impairment
33%
Ophthalmoscopy
33%
Visual Field Test
33%
Survival Analysis
33%
Frameshift Mutation
33%
Color Vision
33%
Vision Test
33%
Biochemistry, Genetics and Molecular Biology
Visual Acuity
100%
Electroretinography
100%
Dark Adaptation
100%
Medical Record
50%
Autofluorescence
50%
Frameshift Mutation
50%
Color Vision
50%