X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (24) 24
humans (23) 23
male (21) 21
female (20) 20
adult (17) 17
ophthalmology (17) 17
electroretinography (13) 13
middle aged (13) 13
adolescent (12) 12
aged (12) 12
mutation (11) 11
child (10) 10
genetic aspects (8) 8
fluorescein angiography (7) 7
gene mutations (7) 7
tomography, optical coherence (7) 7
dna mutational analysis (6) 6
fluorescence (6) 6
genetics (6) 6
medicine & public health (6) 6
retina (6) 6
retinopathy (6) 6
retrospective studies (6) 6
visual acuity (6) 6
visual field tests (6) 6
eye proteins - genetics (5) 5
follow-up studies (5) 5
fundus autofluorescence (5) 5
genetics & heredity (5) 5
retina - physiopathology (5) 5
sense organs (5) 5
young adult (5) 5
child, preschool (4) 4
disease (4) 4
electroretinogram (4) 4
gene (4) 4
heterozygote (4) 4
macular degeneration (4) 4
optical coherence tomography (4) 4
phenotype (4) 4
report (4) 4
visual acuity - physiology (4) 4
visual fields - physiology (4) 4
aged, 80 and over (3) 3
alleles (3) 3
analysis (3) 3
animals (3) 3
article (3) 3
atp-binding cassette transporters - genetics (3) 3
degeneration (3) 3
dysfunction (3) 3
electrooculography (3) 3
electrophysiology (3) 3
electroretinography - methods (3) 3
eye diseases (3) 3
eyes & eyesight (3) 3
gene expression (3) 3
genetic disorders (3) 3
genetic structures (3) 3
macular degeneration - genetics (3) 3
multifocal electroretinography (3) 3
mutations (3) 3
neurosciences (3) 3
night blindness (3) 3
night blindness - physiopathology (3) 3
ophthalmoscopy (3) 3
pedigree (3) 3
physiological aspects (3) 3
research (3) 3
retinal degeneration (3) 3
retinal degeneration - genetics (3) 3
retinal dystrophies - physiopathology (3) 3
retinitis-pigmentosa (3) 3
standard (3) 3
studies (3) 3
visual cortex (3) 3
abridged index medicus (2) 2
adaptor proteins, signal transducing - genetics (2) 2
age (2) 2
bestrophins (2) 2
biochemistry & molecular biology (2) 2
blindness (2) 2
cells (2) 2
central visual field scotomata (2) 2
chloride channels (2) 2
chloroquine retinopathy (2) 2
choroideremia (2) 2
choroideremia - diagnosis (2) 2
choroideremia - genetics (2) 2
choroideremia - physiopathology (2) 2
color perception (2) 2
color perception tests (2) 2
cystoid macular edema (2) 2
diagnosis (2) 2
disease progression (2) 2
dystrophies (2) 2
dystrophy (2) 2
erg (2) 2
fixation, ocular - physiology (2) 2
full-field erg (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Brain Mapping, ISSN 1065-9471, 10/2013, Volume 34, Issue 10, pp. 2607 - 2623
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 09/2010, Volume 87, Issue 3, pp. 376 - 381
Retinitis pigmentosa (RP) is a degenerative disease of the retina leading to progressive loss of vision and, in many instances, to legal blindness at the end... 
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 321 - 330
Journal Article
Journal Article
Human Brain Mapping, ISSN 1065-9471, 10/2013, Volume 34, Issue 10, pp. 2607 - 2623
Journal Article
Journal Article
Journal Article