X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (581) 581
ophthalmology (488) 488
index medicus (412) 412
macular degeneration (325) 325
male (300) 300
stargardt disease (296) 296
female (292) 292
adult (227) 227
stargardt-disease (227) 227
atp-binding cassette transporters - genetics (226) 226
macular degeneration - genetics (219) 219
mutation (207) 207
middle aged (191) 191
animals (182) 182
eye diseases (180) 180
retina (164) 164
retinitis-pigmentosa (152) 152
biochemistry & molecular biology (144) 144
genetic structures (143) 143
aged (142) 142
sense organs (134) 134
abca4 (132) 132
cone-rod dystrophy (122) 122
mutations (118) 118
phenotype (117) 117
adolescent (116) 116
fundus flavimaculatus (116) 116
mice (116) 116
electroretinography (113) 113
child (109) 109
article (107) 107
genetics & heredity (104) 104
macular degeneration - diagnosis (104) 104
lipofuscin (103) 103
fundus oculi (101) 101
macular degeneration - congenital (101) 101
fluorescein angiography (97) 97
dna mutational analysis (96) 96
dystrophy (95) 95
stargardt's disease (92) 92
optical coherence tomography (90) 90
retinal degeneration (90) 90
pedigree (88) 88
retinal pigment epithelium (88) 88
macular degeneration - physiopathology (86) 86
age-related macular degeneration (84) 84
macular dystrophy (84) 84
visual acuity (84) 84
young adult (82) 82
fundus autofluorescence (81) 81
degeneration (80) 80
stargardt macular dystrophy (78) 78
gene (77) 77
photoreceptors (76) 76
retinitis pigmentosa (74) 74
macular degeneration - metabolism (73) 73
macular degeneration - pathology (71) 71
atp-binding cassette transporters - metabolism (70) 70
tomography, optical coherence (70) 70
disease (68) 68
abcr (67) 67
genotype (66) 66
retinal-pigment epithelium (66) 66
retinal degeneration - genetics (62) 62
stargardts-disease (62) 62
alleles (61) 61
disease gene abcr (58) 58
eye proteins - genetics (57) 57
genetic aspects (57) 57
recessive retinitis-pigmentosa (57) 57
genetics (56) 56
retina - metabolism (56) 56
leber congenital amaurosis (55) 55
retinal pigment epithelium - pathology (55) 55
fluorescence (53) 53
geographic atrophy (52) 52
retina - pathology (52) 52
retrospective studies (52) 52
rim protein (52) 52
medicine, research & experimental (51) 51
transporter gene (51) 51
research (50) 50
retinal pigment epithelium - metabolism (50) 50
retinitis pigmentosa - genetics (50) 50
physiological aspects (49) 49
retinoids - metabolism (49) 49
visual cycle (49) 49
lipofuscin - metabolism (48) 48
mouse model (48) 48
a2e (47) 47
visual acuity - physiology (47) 47
disease models, animal (45) 45
abca4 gene (44) 44
analysis (44) 44
light (43) 43
aged, 80 and over (42) 42
genes (41) 41
genetic predisposition to disease (41) 41
cell biology (40) 40
age (39) 39
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (887) 887
German (15) 15
French (12) 12
Turkish (3) 3
Chinese (2) 2
Czech (2) 2
Polish (2) 2
Russian (2) 2
Spanish (2) 2
Japanese (1) 1
Korean (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2018, Volume 1085, pp. 139 - 151
Stargardt disease (STGD) is one of the most common macular dystrophies in young adults. It progresses slowly. Its prevalence is about 1:8000-10,000. Age of... 
Autosomal recessive | Stargardt disease | MEDICINE, RESEARCH & EXPERIMENTAL | OPHTHALMOLOGY | GENETICS & HEREDITY | CELL BIOLOGY
Journal Article
Ophthalmology, ISSN 0161-6420, 2016, Volume 123, Issue 6, pp. 1375 - 1385
Journal Article
Gene Therapy, ISSN 0969-7128, 10/2008, Volume 15, Issue 19, pp. 1311 - 1320
Journal Article
Retina, ISSN 0275-004X, 01/2017, Volume 37, Issue 12, pp. 2352 - 2361
Journal Article
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, ISSN 0275-004X, 07/2019, Volume 39, Issue 7, pp. 1399 - 1409
Purpose: To investigate the natural history of Stargardt disease over a multiyear follow-up. Methods: We reviewed medical records of Stargardt disease... 
natural history study | optical coherence tomography | PHENOTYPE | ATROPHY SECONDARY | VISUAL-ACUITY LOSS | ELECTRORETINOGRAPHIC FINDINGS | AUTOFLUORESCENCE | FLECKS | electrophysiology | PROGSTAR | OPHTHALMOLOGY | Stargardt disease | ABCA4 gene | Macular degeneration | Development and progression | Genotype | Genetic aspects | Health aspects
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 6436 - 11
Fundus autofluorescence (FAF) imaging is crucial to the diagnosis and monitoring of recessive Stargardt disease (STGD1). In a retrospective cohort study of 34... 
VISUALIZATION | MACULAR PIGMENT | SHORT-WAVELENGTH AUTOFLUORESCENCE | LIPOFUSCIN | FUNDUS AUTOFLUORESCENCE | MULTIDISCIPLINARY SCIENCES | NEAR-INFRARED AUTOFLUORESCENCE | STARGARDT DISEASE | FLUORESCEIN ANGIOGRAPHY | MELANIN | RETINAL-PIGMENT EPITHELIUM
Journal Article
Journal Article
Retina, ISSN 0275-004X, 02/2018, Volume 38, Issue 2, pp. 403 - 415
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 1/2019, Volume 257, Issue 1, pp. 41 - 48
To describe the hyperreflective foci (HF) characteristics in eyes affected by Stargardt disease (STGD), correlating HF with the atrophy progression at 1-year... 
Ophthalmology | Stargardt disease | Medicine & Public Health | Optical coherence tomography | Hyperreflective foci | OPHTHALMOLOGY | LESIONS | DEGENERATION | Eye | Atrophy | Retina
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2016, Volume 57, Issue 13, pp. 5186 - 5191
Journal Article
Journal Article