X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2767) 2767
Book / eBook (637) 637
Book Review (580) 580
Publication (299) 299
Newspaper Article (70) 70
Newsletter (44) 44
Magazine Article (40) 40
Book Chapter (28) 28
Government Document (10) 10
Trade Publication Article (6) 6
Conference Proceeding (4) 4
Dissertation (2) 2
Reference (2) 2
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2263) 2263
humans (2224) 2224
ophthalmology (1517) 1517
eye diseases (1503) 1503
male (1301) 1301
female (1240) 1240
eye (876) 876
adult (760) 760
middle aged (609) 609
child (599) 599
genetic structures (533) 533
adolescent (492) 492
sense organs (491) 491
diagnosis (444) 444
surgery (432) 432
diseases (419) 419
child, preschool (415) 415
aged (396) 396
infant (367) 367
research (361) 361
retina (356) 356
mutation (338) 338
abridged index medicus (330) 330
animals (327) 327
care and treatment (322) 322
visual acuity (320) 320
risk factors (262) 262
medicine (237) 237
eyes (234) 234
retrospective studies (231) 231
pedigree (227) 227
glaucoma (219) 219
pediatrics (208) 208
infant, newborn (206) 206
cornea (201) 201
genetic aspects (201) 201
children (196) 196
congenital, hereditary, and neonatal diseases and abnormalities (193) 193
patients (192) 192
medicine & public health (190) 190
analysis (184) 184
macular degeneration (184) 184
health aspects (182) 182
diagnosis, differential (180) 180
article (174) 174
cataract (170) 170
research article (168) 168
young adult (166) 166
disease (165) 165
follow-up studies (165) 165
prevalence (164) 164
eye diseases - complications (158) 158
blindness (155) 155
fluorescein angiography (155) 155
cataracts (148) 148
genetics & heredity (148) 148
phenotype (148) 148
eye diseases - etiology (147) 147
syndrome (147) 147
treatment outcome (146) 146
genetics (145) 145
age (144) 144
tomography, optical coherence (142) 142
aged, 80 and over (139) 139
electroretinography (133) 133
therapy (133) 133
clinical neurology (131) 131
complications and side effects (127) 127
fundus oculi (123) 123
mutations (121) 121
review (120) 120
complications (119) 119
studies (119) 119
neurosciences (118) 118
vision (118) 118
physiological aspects (117) 117
medical research (116) 116
medicine, research & experimental (116) 116
methods (116) 116
management (115) 115
case report (114) 114
genetic disorders (114) 114
optical coherence tomography (114) 114
gene (113) 113
pathology (113) 113
retinoblastoma (112) 112
usage (112) 112
eye diseases - diagnosis (109) 109
mice (108) 108
prospective studies (108) 108
eye manifestations (105) 105
case studies (103) 103
proteins (102) 102
diabetic retinopathy (101) 101
eye diseases, hereditary - complications (101) 101
visual acuity - physiology (100) 100
eyes & eyesight (99) 99
eye movements (98) 98
magnetic resonance imaging (97) 97
retina - pathology (97) 97
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (550) 550
Collection Dvlpm't (Acquisitions) - Closed Orders (23) 23
Collection Dvlpm't (Acquisitions) - Vendor file (17) 17
Online Resources - Online (12) 12
St. Michael's Hospital - Stacks (9) 9
Robarts - Stacks (7) 7
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (7) 7
UTL at Downsview - May be requested (7) 7
Scarborough Hospital - General (5) 5
UofT at Mississauga - Stacks (5) 5
Gerstein Science - Reference (3) 3
Holland Bloorview Kids Rehabilitation - Stacks (3) 3
Humber River Regional Hospital - Finch Stacks (3) 3
Gerstein Science - Circulation Desk (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Royal Ontario Museum - Periodical Stacks (2) 2
Scarborough Hospital - Birchmount (2) 2
Thomas Fisher Rare Book - Rare Book (2) 2
UofT at Scarborough - Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Credit Valley Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - Stacks (1) 1
Gerstein Science - Missing (1) 1
Gerstein Science - Not Returned (1) 1
Gerstein Science - Periodical Stacks (1) 1
Lakeridge Health Sciences - Online (1) 1
Markham Stouffville Hospital - Stacks (1) 1
OISE - Stacks (1) 1
Providence Healthcare - Reference (1) 1
Providence Healthcare - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's Hospital - Circulation Desk (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3462) 3462
French (47) 47
German (46) 46
Spanish (16) 16
Turkish (13) 13
Polish (8) 8
Chinese (7) 7
Italian (6) 6
Japanese (5) 5
Arabic (4) 4
Portuguese (4) 4
Russian (4) 4
Dutch (3) 3
Czech (2) 2
Hebrew (2) 2
Romanian (2) 2
Hungarian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Diabetes Care, ISSN 0149-5992, 10/2017, Volume 40, Issue 10, pp. 1373 - 1378
OBJECTIVE This study investigated the association between renal histology, as assessed by morphometric analysis using light (LM) and electron (EM) microscopy,... 
STRUCTURAL-FUNCTIONAL RELATIONSHIPS | PANCREAS TRANSPLANT RECIPIENTS | BIOPSY | ENDOCRINOLOGY & METABOLISM | RENAL-FUNCTION | INDICATOR | GLOMERULAR HYPERFILTRATION | MELLITUS | NEPHROPATHY | LESIONS | PROGRESSION | Eye Diseases, Hereditary - urine | Intestinal Diseases - complications | Predictive Value of Tests | Follow-Up Studies | Vascular Diseases - complications | Skin Abnormalities - complications | Glycated Hemoglobin A - metabolism | Humans | Middle Aged | Kidney Glomerulus - physiopathology | Male | Diabetic Nephropathies - diagnosis | Diarrhea - urine | Albuminuria - diagnosis | Skin Abnormalities - urine | Adult | Female | Albuminuria - urine | Diarrhea - complications | Diabetes Mellitus, Type 2 - complications | Kidney - physiopathology | Diabetic Nephropathies - urine | Glomerular Filtration Rate | Albuminuria - etiology | Albumins - metabolism | Eye Diseases, Hereditary - complications | Japan | Diabetes Mellitus, Type 2 - urine | Intestinal Diseases - urine | Asian Continental Ancestry Group | Vascular Diseases - urine | Type 2 diabetes | Usage | Care and treatment | Albuminuria | Research | Electron microscopy | Glomerular filtration rate | Urine | Excretion | Kidneys | Diabetes mellitus | Histology | Patients | Studies | Concentration (composition) | Nephropathy | Microscopy | Biopsy | Correlation analysis | Research design | Diabetes | Kidney transplantation | Index Medicus
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 10/2017, Volume 182, pp. 81 - 89
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2015, Volume 21, pp. 88 - 97
Purpose: Aniridia is a rare panocular disorder characterized by iris hypoplasia and other associated eye anomalies. Heterozygous null mutations in paired box... 
DEFECTS | NONSENSE | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | MESSENGER-RNA DECAY | PAX6 GENE | DELETIONS | MISSENSE MUTATIONS | PREDICTION | REGION | Iris - metabolism | Humans | Middle Aged | Cataract - pathology | Child, Preschool | Fovea Centralis - pathology | Male | Nystagmus, Congenital - genetics | Aniridia - genetics | Aniridia - pathology | DNA Mutational Analysis | Nystagmus, Pathologic - complications | Base Sequence | Child | Amino Acid Sequence | Eye Diseases, Hereditary - pathology | Eye Diseases, Hereditary - complications | Repressor Proteins - genetics | Aniridia - complications | Genetic Heterogeneity | India | Cataract - complications | Adolescent | Cataract - genetics | Mutation | Glaucoma - genetics | Paired Box Transcription Factors - genetics | Retinal Diseases - genetics | Nystagmus, Congenital - complications | Nystagmus, Pathologic - genetics | Open Reading Frames | Molecular Sequence Data | Infant | Retinal Diseases - congenital | Case-Control Studies | Retinal Diseases - pathology | Adult | Female | Eye Proteins - genetics | Nystagmus, Pathologic - pathology | Fovea Centralis - abnormalities | Genetic Association Studies | Introns | Retinal Diseases - complications | PAX6 Transcription Factor | Glaucoma - complications | Iris - pathology | Homeodomain Proteins - genetics | Eye Diseases, Hereditary - genetics | Haploinsufficiency | Nystagmus, Congenital - pathology | Aged | Glaucoma - pathology | Index Medicus
Journal Article
Journal Article
Japanese Journal of Ophthalmology, ISSN 0021-5155, 3/2019, Volume 63, Issue 2, pp. 172 - 180
To report the findings in 3 cases of bilateral negative electroretinograms (ERGs) with acute onset of photophobia.Retrospective case series.The medical charts... 
Negative-type ERG | Post-phototransduction abnormality | Ophthalmology | Medicine & Public Health | Incomplete-type congenital stationary night blindness | Acquired retinal disease | AUTOANTIBODIES | EYES | PHOTOPIC ELECTRORETINOGRAM | RESPONSES | RETINAL DYSTROPHY | OPHTHALMOLOGY | CONE DYSTROPHY | RETINOPATHY | MUTATIONS | NEGATIVE ELECTRORETINOGRAM | STATIONARY NIGHT BLINDNESS | Electroretinography - methods | Follow-Up Studies | Photophobia - etiology | Humans | Genetic Diseases, X-Linked - complications | Eye Diseases, Hereditary - diagnosis | Myopia - diagnosis | Night Blindness - complications | Adult | Female | Retrospective Studies | Genetic Diseases, X-Linked - physiopathology | Fluorescein Angiography | Myopia - complications | Acute Disease | Diagnosis, Differential | Eye Diseases, Hereditary - physiopathology | Eye Diseases, Hereditary - complications | Tomography, Optical Coherence | Night Blindness - diagnosis | Photophobia - diagnosis | Visual Acuity | Genetic Diseases, X-Linked - diagnosis | Myopia - physiopathology | Night Blindness - physiopathology | Aged | Fundus Oculi | Medical colleges | Analysis | Genetic disorders | Angiography | Abnormalities | Retina | Visual acuity | Nyctalopia | Patients | Acuity | Electroretinograms | Optical Coherence Tomography | Fluorescein | Genetic analysis | Blindness | Eye diseases | Stationary night blindness | Visual fields | Index Medicus
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 08/2015, Volume 181, Issue 2, pp. 338 - 342
Journal Article
Journal of Medical Case Reports, ISSN 1752-1947, 05/2017, Volume 11, Issue 1, pp. 135 - 135
Castleman disease is a rare lymphoproliferative disorder presenting with localized or disseminated lymphadenopathy and systemic manifestations. It can be... 
Hyaline-vascular | Case report | Multiple system involvement | Sri Lanka | Castleman disease | Rituximab | Multicentric | Hepatomegaly - pathology | Intestinal Diseases - complications | Castleman Disease - drug therapy | Vascular Diseases - complications | Skin Abnormalities - complications | Humans | Castleman Disease - diagnosis | Eye Diseases, Hereditary - diagnosis | Lymphadenopathy - etiology | Proteinuria - pathology | Skin Abnormalities - diagnosis | Rituximab - therapeutic use | Adult | Female | Skin Abnormalities - drug therapy | Diarrhea - complications | Vascular Diseases - drug therapy | Proteinuria - etiology | Eye Diseases, Hereditary - complications | Intestinal Diseases - drug therapy | Treatment Outcome | Antihypertensive Agents - therapeutic use | Vascular Diseases - diagnosis | Eye Diseases, Hereditary - drug therapy | Diarrhea - diagnosis | Intestinal Diseases - diagnosis | Lymphadenopathy - pathology | Castleman Disease - complications | Diuretics - therapeutic use | Diarrhea - drug therapy | Sentinel Lymph Node Biopsy | Hepatomegaly - etiology | Immunologic Factors - therapeutic use | Care and treatment | Lymphoproliferative disorders | Diagnosis | Risk factors | Urine | Lymphatic system | Kidneys | Hematology | Laboratories | Cancer therapies | Blood | Proteins | Case studies | Hepatitis | Biopsy |