X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (896) 896
Book Review (345) 345
Publication (64) 64
Book / eBook (33) 33
Book Chapter (20) 20
Newsletter (15) 15
Newspaper Article (10) 10
Magazine Article (9) 9
Conference Proceeding (3) 3
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (711) 711
humans (677) 677
ophthalmology (297) 297
male (256) 256
mutation (241) 241
dna, mitochondrial - genetics (217) 217
female (211) 211
mitochondrial dna (207) 207
hereditary optic neuropathy (196) 196
animals (185) 185
optic atrophy, hereditary, leber - genetics (182) 182
adult (169) 169
clinical neurology (153) 153
eye diseases (153) 153
mitochondria (146) 146
neurosciences (132) 132
genetic structures (115) 115
optic atrophy (115) 115
optic nerve (113) 113
optic neuropathy (111) 111
disease (108) 108
genetics & heredity (103) 103
middle aged (102) 102
adolescent (95) 95
child (90) 90
genetic aspects (89) 89
diagnosis (84) 84
retina (83) 83
optic atrophy, hereditary, leber - therapy (81) 81
neurology (78) 78
multiple sclerosis (77) 77
gene therapy (76) 76
mutations (75) 75
leber's hereditary optic neuropathy (74) 74
sense organs (74) 74
biochemistry & molecular biology (73) 73
research (73) 73
cell biology (72) 72
mitochondrial diseases - genetics (71) 71
optic neuritis (70) 70
analysis (69) 69
mitochondria - metabolism (69) 69
optic atrophy, hereditary, leber - diagnosis (69) 69
visual acuity (69) 69
glaucoma (67) 67
neuropathy (67) 67
magnetic resonance imaging (66) 66
care and treatment (64) 64
lhon (62) 62
oxidative stress (62) 62
abridged index medicus (61) 61
disease models, animal (61) 61
medicine & public health (60) 60
blindness (59) 59
point mutation (58) 58
diagnosis, differential (57) 57
mitochondria - genetics (57) 57
atrophy (56) 56
mice (56) 56
article (54) 54
optic atrophies, hereditary - genetics (54) 54
visual fields (54) 54
genes (53) 53
genetics (53) 53
aged (52) 52
mitochondrial disease (52) 52
gene mutations (51) 51
leber hereditary optic neuropathy (51) 51
medicine (51) 51
medicine, research & experimental (50) 50
pedigree (50) 50
retinal ganglion cells - pathology (50) 50
genetic therapy (49) 49
retinal ganglion cells (49) 49
dna mutational analysis (48) 48
idebenone (48) 48
optic atrophy, hereditary, leber - physiopathology (48) 48
mouse model (47) 47
physiological aspects (47) 47
optic atrophy, hereditary, leber - drug therapy (46) 46
optic atrophy, hereditary, leber - pathology (46) 46
multiple-sclerosis (45) 45
patients (45) 45
risk factors (45) 45
young adult (45) 45
mtdna (44) 44
ubiquinone - analogs & derivatives (44) 44
health aspects (42) 42
pediatrics (42) 42
eye (41) 41
optic atrophy, hereditary, leber - complications (41) 41
review (41) 41
vision (41) 41
dna (40) 40
mitochondrial diseases (39) 39
therapy (39) 39
complex-i (38) 38
dominant optic atrophy (38) 38
gene (38) 38
mitochondrial-dna mutation (38) 38
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (27) 27
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Periodical Stacks (1) 1
Gerstein Science - Reference (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
UTL at Downsview - May be requested (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (927) 927
French (14) 14
German (10) 10
Japanese (7) 7
Spanish (7) 7
Chinese (3) 3
Czech (2) 2
Russian (2) 2
Danish (1) 1
Dutch (1) 1
Hebrew (1) 1
Hungarian (1) 1
Korean (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Lancet, The, ISSN 0140-6736, 2009, Volume 374, Issue 9701, pp. 1597 - 1605
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 04/2014, Volume 132, Issue 4, pp. 409 - 420
Journal Article
Journal Article
Archivos de la Sociedad Espanola de Oftalmologia, 12/2016, Volume 91, Issue 12, p. 559
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2013, Volume 21, Issue 1, pp. 62 - 68
Journal Article
Journal Article
Journal Article