Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1153) 1153
Book Chapter (67) 67
Magazine Article (6) 6
Newspaper Article (5) 5
Book / eBook (2) 2
Dissertation (2) 2
Newsletter (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (964) 964
science & technology (807) 807
life sciences & biomedicine (773) 773
male (618) 618
ophthalmology (539) 539
female (511) 511
adult (432) 432
mutation (362) 362
dna, mitochondrial - genetics (321) 321
optic atrophy, hereditary, leber - genetics (299) 299
biological and medical sciences (267) 267
middle aged (267) 267
medical sciences (258) 258
adolescent (251) 251
neurosciences & neurology (220) 220
mitochondrial dna (215) 215
optic atrophy, hereditary, leber - diagnosis (213) 213
child (212) 212
eye diseases (206) 206
clinical neurology (198) 198
pedigree (197) 197
optic atrophies, hereditary - genetics (181) 181
optic atrophy (172) 172
optic neuropathy (163) 163
genetic structures (159) 159
optic nerve (158) 158
visual acuity (150) 150
dna mutational analysis (148) 148
neurology (143) 143
genetics & heredity (139) 139
optic atrophies, hereditary - diagnosis (136) 136
magnetic resonance imaging (123) 123
young adult (122) 122
aged (118) 118
diagnosis, differential (113) 113
leber's hereditary optic neuropathy (108) 108
neurosciences (108) 108
genetic aspects (106) 106
sense organs (106) 106
diagnosis (103) 103
point mutation (102) 102
mitochondria (96) 96
patients (94) 94
child, preschool (93) 93
abridged index medicus (92) 92
diseases of visual field, optic nerve, optic chiasma and optic tracts (91) 91
polymerase chain reaction (91) 91
optic neuritis (90) 90
retina (89) 89
neuropathy (87) 87
research (86) 86
medicine & public health (79) 79
multiple sclerosis (79) 79
optic nerve diseases - diagnosis (78) 78
visual fields (77) 77
tomography, optical coherence (73) 73
optic atrophy, hereditary, leber - complications (71) 71
retinal ganglion cells - pathology (71) 71
optic atrophy, hereditary, leber - physiopathology (70) 70
risk factors (69) 69
leber hereditary optic neuropathy (67) 67
optic nerve - pathology (64) 64
gene mutations (63) 63
phenotype (63) 63
care and treatment (62) 62
genetics (62) 62
optical coherence tomography (62) 62
animals (59) 59
atrophy (59) 59
deoxyribonucleic acid--dna (59) 59
glaucoma (59) 59
research article (59) 59
medicine (57) 57
analysis (56) 56
visual acuity - physiology (56) 56
electroretinography (55) 55
optic atrophy, autosomal dominant - genetics (54) 54
optic disk - pathology (54) 54
pediatrics (54) 54
blindness (53) 53
nerve fibers - pathology (53) 53
optic atrophy, hereditary, leber - pathology (53) 53
molecular sequence data (52) 52
mutation - genetics (52) 52
retrospective studies (52) 52
infant (51) 51
fluorescein angiography (49) 49
gtp phosphohydrolases - genetics (49) 49
retinopathies (49) 49
follow-up studies (48) 48
lhon (47) 47
optics (47) 47
age (46) 46
biochemistry & molecular biology (46) 46
tomography (46) 46
optic atrophy - diagnosis (45) 45
base sequence (44) 44
genes (44) 44
optic atrophy - genetics (44) 44
disease (43) 43
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1151) 1151
German (28) 28
French (23) 23
Japanese (22) 22
Russian (10) 10
Spanish (10) 10
Chinese (7) 7
Polish (6) 6
Czech (4) 4
Portuguese (4) 4
Croatian (1) 1
Dutch (1) 1
Finnish (1) 1
Hebrew (1) 1
Hungarian (1) 1
Italian (1) 1
Korean (1) 1
Romanian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Trial end points and natural history in patients with G11778A leber hereditary optic neuropathy: Preparation for gene therapy clinical trial
by Lam, Byron L and Feuer, William J and Schiffman, Joyce C and Porciatti, Vittorio and Vandenbroucke, Ruth and Rosa, Potyra R and Gregori, Giovanni and Guy, John
JAMA ophthalmology, ISSN 2168-6165, 2014, Volume 132, Issue 4, pp. 428 - 436
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Dependovirus - genetics | Genetic Therapy | Visual Fields - physiology | Prospective Studies | Intravitreal Injections | Humans | Middle Aged | Male | NADH Dehydrogenase - genetics | Optic Atrophy, Hereditary, Leber - genetics | Retinal Ganglion Cells - metabolism | Retinal Ganglion Cells - pathology | Young Adult | DNA, Mitochondrial - genetics | DNA Mutational Analysis | Endpoint Determination | Adult | Female | Optic Atrophy, Hereditary, Leber - diagnosis | Child | Visual Acuity - physiology | Electroretinography | Nerve Fibers - pathology | Tomography, Optical Coherence | Clinical Trials as Topic | Optic Atrophy, Hereditary, Leber - therapy | Adolescent | Visual Field Tests | Genetic Vectors
Journal Article
Details down arrow
2. Full Text Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series
by Hwang, Tiffany Jean and Karanjia, Rustum and Moraes-Filho, Milton Nunes and Gale, Jesse and Tran, Jeffrey Show and Chu, Edward R and Salomao, Solange R and Berezovsky, Adriana and Belfort, Rubens and Moraes, Milton Nunes and Sadun, Federico and DeNegri, Anna Maria and La Morgia, Chiara and Barboni, Piero and Ramos, Carolina do V.F and Chicani, Carlos Filipe and Quiros, Peter A and Carelli, Valerio and Sadun, Alfredo A
Ophthalmology (Rochester, Minn.), ISSN 0161-6420, 06/2017, Volume 124, Issue 6, pp. 843 - 850
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Nerve Fibers - pathology | Visual Fields - physiology | Prospective Studies | Tomography, Optical Coherence | Humans | Middle Aged | Male | Optic Atrophy, Hereditary, Leber - genetics | Retinal Ganglion Cells - pathology | Young Adult | Vision Disorders - diagnosis | Vision Disorders - physiopathology | DNA, Mitochondrial - genetics | Pedigree | Adolescent | Adult | Female | Visual Field Tests | Optic Atrophy, Hereditary, Leber - diagnosis | Visual Acuity - physiology | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Inherited mitochondrial optic neuropathies
by Yu-Wai-Man, P and Griffiths, P G and Hudson, G and Chinnery, P F
Journal of Medical Genetics, ISSN 0022-2593, 03/2009, Volume 46, Issue 3, pp. 145 - 158
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Optic Atrophy, Autosomal Dominant - diagnosis | Humans | Optic Atrophy, Hereditary, Leber - epidemiology | DNA, Mitochondrial | Male | Optic Atrophy, Hereditary, Leber - genetics | Point Mutation | Optic Atrophy, Autosomal Dominant - epidemiology | Optic Atrophy, Hereditary, Leber - pathology | GTP Phosphohydrolases - genetics | Optic Atrophy, Autosomal Dominant - genetics | Female | Optic Atrophy, Autosomal Dominant - pathology | Optic Atrophy, Hereditary, Leber - diagnosis | Physiological aspects | Development and progression | Mitochondrial DNA | Genetic aspects | Leber's congenital amaurosis | Ganglion | Risk factors | Hypotheses | Optic nerve | Disease | Mutation | Family medical history | Age | Index Medicus | 1507 | 1506 | Review
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategies
by Yu-Wai-Man, Patrick and Griffiths, Philip G and Chinnery, Patrick F
Progress in retinal and eye research, ISSN 1350-9462, 03/2011, Volume 30, Issue 2, pp. 81 - 114
Glaucoma | Hereditary spastic paraplegia | Dominant optic atrophy | Neuroprotection | Multiple sclerosis | Mitofusin | Optic neuropathy | Optic neuritis | Leber hereditary optic neuropathy | Mitochondrial DNA | Retinal ganglion cell | Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Optic Nerve - pathology | Humans | Optic Atrophy, Hereditary, Leber - therapy | Retinal Ganglion Cells - pathology | Point Mutation | Optic Atrophy, Hereditary, Leber - pathology | Phenotype | Animals | DNA, Mitochondrial - genetics | Optic Atrophy, Autosomal Dominant - therapy | Optic Atrophy, Autosomal Dominant - pathology | Optic Atrophy, Autosomal Dominant - physiopathology | Optic Atrophy, Hereditary, Leber - physiopathology | Disease Models, Animal | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights