X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (18) 18
humans (14) 14
ophthalmology (13) 13
female (12) 12
male (10) 10
middle aged (9) 9
adult (8) 8
adolescent (6) 6
aged (6) 6
mutation (6) 6
mutations (6) 6
phenotype (6) 6
child (5) 5
genetic aspects (5) 5
young adult (5) 5
aged, 80 and over (4) 4
eye diseases (4) 4
genetics (4) 4
pseudoxanthoma elasticum (4) 4
retinitis pigmentosa (4) 4
visual acuity - physiology (4) 4
analysis (3) 3
atp-binding cassette transporters - genetics (3) 3
belgium (3) 3
dna mutational analysis (3) 3
electroretinography (3) 3
expression (3) 3
eye proteins - genetics (3) 3
gene (3) 3
genetics & heredity (3) 3
health aspects (3) 3
proteins (3) 3
research (3) 3
retina (3) 3
retinal pigment epithelium - pathology (3) 3
retinitis pigmentosa - genetics (3) 3
sense organs (3) 3
antisense oligonucleotides (2) 2
article (2) 2
atherosclerosis (2) 2
biology and life sciences (2) 2
blindness (2) 2
child, preschool (2) 2
choroidal neovascularization (2) 2
classification (2) 2
clinical neurology (2) 2
cohort studies (2) 2
color perception tests (2) 2
deficiency (2) 2
dystrophy (2) 2
fluorescein angiography (2) 2
further section (2) 2
genetic association studies (2) 2
genetic structures (2) 2
genetic testing (2) 2
heterozygote (2) 2
identification (2) 2
infant (2) 2
infrared rays (2) 2
lipofuscin (2) 2
macular degeneration (2) 2
macular degeneration - congenital (2) 2
macular degeneration - genetics (2) 2
medicine (2) 2
medicine & public health (2) 2
medicine and health sciences (2) 2
multimodal imaging (2) 2
pathology (2) 2
photoreceptors (2) 2
prevalence (2) 2
retinal diseases (2) 2
retinal-pigment epithelium (2) 2
retinitis pigmentosa - physiopathology (2) 2
retrospective studies (2) 2
reveals (2) 2
risk factors (2) 2
spectrum (2) 2
splicing (2) 2
tomography, optical coherence (2) 2
1 (1) 1
4 (1) 1
abca (1) 1
abca4 (1) 1
abca4 gene (1) 1
abca4-associated disease (1) 1
abcc6 (1) 1
abcc6 gene (1) 1
aberrant disulfide bonding (1) 1
acquired colour vision defect (1) 1
acta2 mutation (1) 1
actins - genetics (1) 1
activation (1) 1
acuity (1) 1
administration, cutaneous (1) 1
age-related accumulation (1) 1
alleles (1) 1
allergens (1) 1
allergic contact dermatitis (1) 1
angiogenesis (1) 1
angioid streaks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Contact Dermatitis, ISSN 0105-1873, 01/2016, Volume 74, Issue 1, pp. 18 - 21
Journal Article
Open Ophthalmology Journal, ISSN 1874-3641, 08/2016, Volume 10, Issue 1, pp. 160 - 165
To describe a patient with bilateral multifocal choroidal metastases from an endobronchial carcinoid treated with a somatostatin analogue. A 60-year-old woman... 
Somatostatin analogues | Carcinoid tumor | Chromogranine A | Choroidal metastases
Journal Article
Journal Article
Clinical and Translational Allergy, ISSN 2045-7022, 07/2014, Volume 4, Issue S3, pp. P85 - P85
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 2013, Volume 4, pp. 14 - 14
Pseudoxanthoma elasticum (PXE) is an inherited multi-system disorder characterized by ectopic mineralization and fragmentation of elastic fibers in the skin,... 
Retina | Bruch's membrane | Pseudoxanthoma elasticum | Choroidal neovascularization | Angioid streaks | Choroidal Neovascularization | Pseudoxanthoma Elasticum | Angioid Streaks | Bruch Membrane
Journal Article
Nephron, ISSN 1660-8151, 08/2018, Volume 140, Issue 1, pp. 63 - 73
Thrombomodulin (TM) is an endothelial glycoprotein that is present in all blood vessels. Five percent of all patients with atypical hemolytic uremic syndrome... 
Experimental Nephrology and Genetics: Review | Endothelial | Thrombotic microangiopathy | Malignant hypertension | Thrombomodulin | COMPLEMENT | ACTIVATION | PREDICTOR | EFFICACY | ATHEROSCLEROSIS | REPERFUSION | PROTEIN-C | HUMAN SOLUBLE THROMBOMODULIN | UROLOGY & NEPHROLOGY | MUTATIONS | EXPRESSION
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2018, Volume 21, Issue 6, pp. 1319 - 1329
RAX2 encodes a homeobox-containing transcription factor, in which four monoallelic pathogenic variants have been described in autosomal dominant cone-dominated... 
retinitis pigmentosa | homeobox-containing transcription factor | loss of function | novel ARRP gene | RAX2
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 11/2013, Volume 33, Issue 11, pp. 2646 - 2652
Journal Article
Journal of Ocular Pharmacology and Therapeutics, ISSN 1080-7683, 12/2018, Volume 34, Issue 10, pp. 710 - 719
To evaluate the efficacy of dexamethasone intravitreal implants (DEX implant) in patients with treatment-resistant macular edema (ME) owing to branch and... 
dexamethasone | retinal vein occlusion | macular edema | vitrectomy | treatment-resistant | Ozurdex | VISUAL-ACUITY | EYES | SAFETY | SECONDARY | BEVACIZUMAB AVASTIN | TRIAMCINOLONE ACETONIDE | THERAPY | OPHTHALMOLOGY | PHARMACOLOGY & PHARMACY
Journal Article
Journal Article