X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (270) 270
Publication (49) 49
Book / eBook (31) 31
Newspaper Article (10) 10
Book Review (8) 8
Dissertation (7) 7
Conference Proceeding (4) 4
Magazine Article (3) 3
Book Chapter (2) 2
Compact Disc (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (146) 146
humans (127) 127
male (82) 82
female (80) 80
ophthalmology (75) 75
middle aged (65) 65
adult (64) 64
mutation (55) 55
adolescent (52) 52
retinitis-pigmentosa (44) 44
animals (41) 41
child (40) 40
optical coherence tomography (40) 40
electroretinography (36) 36
retina (34) 34
tomography, optical coherence (34) 34
aged (33) 33
eye proteins - genetics (32) 32
leber congenital amaurosis (31) 31
retinal degeneration - genetics (31) 31
genetics & heredity (30) 30
retinal degeneration (29) 29
eye diseases (27) 27
photoreceptors (27) 27
retina - pathology (25) 25
article (23) 23
child, preschool (23) 23
genetic structures (23) 23
mice (23) 23
sense organs (23) 23
cis-trans-isomerases (22) 22
mouse model (20) 20
gene therapy (19) 19
phenotype (19) 19
genetic aspects (18) 18
retinitis pigmentosa - genetics (18) 18
analysis (17) 17
blindness (17) 17
childhood blindness (17) 17
macular degeneration (17) 17
research (17) 17
retinal degeneration - physiopathology (17) 17
visual acuity (17) 17
carrier proteins - genetics (16) 16
degeneration (16) 16
retina - metabolism (16) 16
visual field tests (16) 16
young adult (16) 16
blindness - therapy (15) 15
disease models, animal (15) 15
health aspects (15) 15
retinal degeneration - diagnosis (15) 15
blindness - genetics (14) 14
rod (14) 14
biochemistry & molecular biology (13) 13
expression (13) 13
genetic therapy (13) 13
medicine, research & experimental (13) 13
mutations (13) 13
photoreceptor cells, vertebrate - pathology (13) 13
visual acuity - physiology (13) 13
biotechnology & applied microbiology (12) 12
care and treatment (12) 12
cone-rod dystrophy (12) 12
medicine, general & internal (12) 12
visual fields - physiology (12) 12
abridged index medicus (11) 11
aged, 80 and over (11) 11
dependovirus - genetics (11) 11
diagnosis (11) 11
disease (11) 11
gene (11) 11
risk factors (11) 11
visual cycle (11) 11
canine model (10) 10
cone (10) 10
dark adaptation (10) 10
dogs (10) 10
gene-therapy (10) 10
multidisciplinary sciences (10) 10
pedigree (10) 10
physiological aspects (10) 10
retinal pigment epithelium (10) 10
retinitis pigmentosa - physiopathology (10) 10
rpe65 mutations (10) 10
articles (9) 9
biological sciences (9) 9
blindness - congenital (9) 9
carrier proteins (9) 9
dna mutational analysis (9) 9
eyes (9) 9
genetic therapy - methods (9) 9
genetics (9) 9
infant (9) 9
photoreceptor cells, vertebrate - physiology (9) 9
photoreceptor degeneration (9) 9
prospective studies (9) 9
proteins - genetics (9) 9
retinitis pigmentosa (9) 9
retrospective studies (9) 9
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (17) 17
UTL at Downsview - May be requested (11) 11
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Music - Circulation Desk (1) 1
Robarts - Storage (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


JAMA Ophthalmology, ISSN 2168-6165, 04/2017, Volume 135, Issue 4, p. 320
Importance Detecting elevated intracranial pressure in children with subacute conditions, such as craniosynostosis or tumor, may enable timely intervention and... 
Hypertension | Hydrocephalus | Craniosynostosis | Retina | Cognition | Pressure | Children & youth | Surgery | Tomography | Skull | Children | Ophthalmology | Tumors
Journal Article
2011, 1. ed., Textos universitarios / Anroart, ISBN 9788415148326, Volume 31, 175
Book
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2012, Volume 109, Issue 6, pp. 2132 - 2137
Hereditary retinal blindness is caused by mutations in genes expressed in photoreceptors or retinal pigment epithelium. Gene therapy in mouse and dog models of... 
Eyes | Disease vectors | Disease models | Canines | Retinitis pigmentosa | Photoreceptors | Retina | Gene therapy | Retinal diseases | Genetic mutation | Retinal degeneration | MUTATION ANALYSIS | retinal degeneration | LEBER CONGENITAL AMAUROSIS | CHILDHOOD BLINDNESS | CANINE MODEL | retina | CONE VISION | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | RPGR EXON ORF15 | GTPASE REGULATOR RPGR | DISEASE EXPRESSION | Genetic Therapy | Retinal Bipolar Cells - pathology | Humans | Retinitis Pigmentosa - genetics | Genotype | Eye Proteins - therapeutic use | Mutation - genetics | Open Reading Frames - genetics | Blindness - genetics | Protein Transport | Phenotype | Animals | Retinitis Pigmentosa - therapy | Dogs | Opsins - metabolism | Genetic Diseases, X-Linked - genetics | Mice | Blindness - therapy | Eye Proteins - genetics | Photoreceptor Cells, Vertebrate - pathology | Genetic Diseases, X-Linked - therapy | Care and treatment | Blindness | Physiological aspects | Genetic aspects | Research | Health aspects | Proteins | Mutation | Gene expression | Animal models | Translation | Preservation | X chromosome | Clinical trials | Rod outer segment membranes | Nuclei | Promoters | interphotoreceptor retinoid-binding protein | Cones | Bipolar cells | retinal pigment epithelium | Guanosinetriphosphatase | Index Medicus | Biological Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2008, Volume 105, Issue 39, pp. 15112 - 15117
Journal Article
Human Gene Therapy, ISSN 1043-0342, 10/2008, Volume 19, Issue 10, pp. 979 - 990
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 05/2017, Volume 135, Issue 5, p. 487
Importance The diagnostic path presented narrows down the cause of acute vision loss to the cone photoreceptor outer segment and will refocus the search for... 
Retinopathy | Visual field | Color | Retina | I.R. radiation | Rod outer segment membranes | Epithelium | Retinal pigment epithelium | Acuity | Electroretinograms | Eye | Color vision | Vision | Blindness | Acetylcholine receptors | Boys | Teenagers | Ophthalmology | Structure-function relationships
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2009, Volume 361, Issue 7, pp. 725 - 727
To the Editor: Leber's congenital amaurosis, a common cause of blindness in infants and children, 1 recently became the first human genetic retinal disease to... 
MEDICINE, GENERAL & INTERNAL | Genetic Therapy | Blindness - physiopathology | Humans | Retinal Degeneration - therapy | Female | Blindness - congenital | Blindness - therapy | Retinal Degeneration - congenital | Retinal Degeneration - physiopathology | Fixation, Ocular | Contrast Sensitivity | Gene therapy | Retina | Index Medicus | Abridged Index Medicus
Journal Article
Molecular Therapy, ISSN 1525-0016, 12/2005, Volume 12, Issue 6, pp. 1072 - 1082
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 10/2017, Volume 135, Issue 10, pp. 1069 - 1076
Journal Article
Journal Article
Journal Article