X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1579) 1579
Patent (572) 572
Book Review (55) 55
Conference Proceeding (38) 38
Publication (25) 25
Book Chapter (21) 21
Book / eBook (6) 6
Dissertation (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (729) 729
humans (640) 640
female (352) 352
male (343) 343
middle aged (233) 233
adult (218) 218
clinical neurology (210) 210
neurosciences (206) 206
aged (187) 187
chemistry (187) 187
metallurgy (173) 173
human necessities (161) 161
animals (155) 155
mutation (136) 136
mechanical engineering (132) 132
heating (131) 131
blasting (130) 130
lighting (130) 130
weapons (129) 129
performing operations (117) 117
transporting (117) 117
engineering elements and units (113) 113
general measures for producing and maintaining effectivefunctioning of machines or installations (113) 113
thermal insulation in general (113) 113
belts, cables, or ropes, predominantly used for drivingpurposes (108) 108
chains (108) 108
fittings predominantly used therefor (108) 108
genetics & heredity (102) 102
neurology (98) 98
organic chemistry (98) 98
physics (97) 97
hygiene (93) 93
medical or veterinary science (93) 93
mice (90) 90
pedigree (88) 88
japan (85) 85
electricity (82) 82
preparations for medical, dental, or toilet purposes (80) 80
molecular sequence data (77) 77
adolescent (75) 75
child (75) 75
abridged index medicus (73) 73
biochemistry (72) 72
microbiology (70) 70
gene (68) 68
analysis (67) 67
base sequence (66) 66
aged, 80 and over (65) 65
heterocyclic compounds (63) 63
beer (62) 62
enzymology (62) 62
mutation or genetic engineering (62) 62
spirits (62) 62
vinegar (61) 61
wine (61) 61
specific therapeutic activity of chemical compounds ormedicinal preparations (60) 60
biochemistry & molecular biology (59) 59
amusements (58) 58
card, board, or roulette games (58) 58
games (58) 58
games not otherwise provided for (58) 58
genetic aspects (58) 58
indoor games using small moving playing bodies (58) 58
sports (58) 58
video games (57) 57
magnetic resonance imaging (55) 55
disease (53) 53
research (53) 53
photography (50) 50
cinematography (49) 49
electrography (49) 49
holography (49) 49
amino acid sequence (47) 47
dna mutational analysis (47) 47
electric communication technique (45) 45
amyotrophic lateral sclerosis (43) 43
child, preschool (43) 43
medicine & public health (43) 43
expression (42) 42
genes (42) 42
genetics (42) 42
ataxia (41) 41
basic electric elements (41) 41
genotype (41) 41
phenotype (41) 41
age of onset (39) 39
brain - pathology (39) 39
medical colleges (39) 39
oncology (39) 39
compositions based thereon (38) 38
organic macromolecular compounds (38) 38
protein (38) 38
their preparation or chemical working-up (38) 38
nerve tissue proteins - genetics (37) 37
brain (36) 36
chromosome mapping (36) 36
electrophotography (36) 36
general tagging of cross-sectional technologies spanning over several sections of the ipc (36) 36
general tagging of new technological developments (36) 36
magnetography (36) 36
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Art - Library use only (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Gerstein Science - Stacks (2) 2
Robarts - Stacks (2) 2
Royal Ontario Museum - Far Eastern (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Online Resources - Online (1) 1
Royal Ontario Museum - Archives (1) 1
Royal Ontario Museum - Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2087) 2087
Japanese (139) 139
French (71) 71
German (56) 56
Chinese (14) 14
Korean (2) 2
Spanish (2) 2
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Gastric Cancer, ISSN 1436-3291, 7/2016, Volume 19, Issue 3, pp. 968 - 976
Journal Article
JAMA Neurology, ISSN 2168-6149, 06/2013, Volume 70, Issue 6, pp. 689 - 689
  The availability of high-throughput genome sequencing technologies is expected to revolutionize our understanding of not only hereditary neurological... 
Genomes | Genetic disorders | Mutation | Clinical medicine | Genes | Neurological disorders
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, pp. e58618 - e58618
Journal Article
Neurology, ISSN 0028-3878, 03/2017, Volume 88, Issue 13, pp. 1296 - 1296
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 2014, Volume 371, Issue 1, pp. 82 - 83
Journal Article
by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium and Oncology and Pathology, Kamprad Lab and Lund University and Lunds universitet and Onkologi och Patologi, Kampradlab
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Summary Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large... 
Neurology | PREVALENCE | MUTATIONS | LOBAR DEGENERATION | GENETICS | TDP-43 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Index Medicus | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Genomics, ISSN 0888-7543, 2009, Volume 93, Issue 5, pp. 441 - 448
Journal Article
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, ISSN 0021-5384, 09/2015, Volume 104, Issue 9, pp. 1924 - 1929
Journal Article
Nihon Jibiinkoka Gakkai kaiho, ISSN 0030-6622, 12/2014, Volume 117, Issue 12, pp. 1423 - 1430
Journal Article
Neurology and Clinical Neuroscience, ISSN 2049-4173, 09/2016, Volume 4, Issue 5, pp. 189 - 191
We describe sibling cases presenting with long‐standing, slowly progressive proximal muscle weakness without joint contractures or hyperlaxity. Whole‐exome... 
mutation | muscle disease/neuromuscular junction | Bethlem myopathy | COL6A2 | neurogenetics | Genotype & phenotype | Muscular dystrophy | Mutation
Journal Article
Clinical Neurology, ISSN 0009-918X, 2014, Volume 54, Issue 12, pp. 969 - 971
Journal Article
Nihon Naika Gakkai Zasshi, ISSN 0021-5384, 2015, Volume 104, Issue 9, pp. 1924 - 1929
Journal Article
Nihon Naika Gakkai Zasshi, ISSN 0021-5384, 2015, Volume 104, Issue Suppl, pp. 117 - 118a
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 7, pp. 505 - 512
Journal Article
Journal Article