X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (39193) 39193
Newspaper Article (4299) 4299
Newsletter (1811) 1811
Book Chapter (247) 247
Magazine Article (184) 184
Government Document (120) 120
Book / eBook (70) 70
Trade Publication Article (53) 53
Dissertation (52) 52
Book Review (32) 32
Conference Proceeding (25) 25
Publication (24) 24
Web Resource (22) 22
Reference (15) 15
Transcript (9) 9
Streaming Video (3) 3
Journal / eJournal (2) 2
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
stroke (33271) 33271
humans (24025) 24025
male (17822) 17822
female (14817) 14817
risk factors (10674) 10674
middle aged (10393) 10393
aged (9055) 9055
animals (8806) 8806
neurosciences (7877) 7877
adult (7102) 7102
ischemia (6947) 6947
research (6762) 6762
clinical neurology (5775) 5775
brain (5689) 5689
medicine (5600) 5600
neurology (5473) 5473
studies (4975) 4975
multidisciplinary sciences (4876) 4876
mortality (4562) 4562
research article (4538) 4538
hypertension (4491) 4491
cardiovascular disease (4426) 4426
risk (4397) 4397
analysis (4355) 4355
patients (4188) 4188
science (4050) 4050
cardiovascular diseases (3907) 3907
medical research (3904) 3904
peripheral vascular disease (3725) 3725
health aspects (3605) 3605
mice (3593) 3593
disease (3570) 3570
rats (3477) 3477
genetic aspects (3435) 3435
care and treatment (3428) 3428
stroke - genetics (3307) 3307
ischemic-stroke (3279) 3279
aged, 80 and over (3239) 3239
ischemic stroke (3158) 3158
cardiac & cardiovascular systems (3153) 3153
atherosclerosis (3102) 3102
inflammation (3056) 3056
diabetes (2966) 2966
magnetic resonance imaging (2784) 2784
genetics (2761) 2761
medicine, experimental (2648) 2648
disease models, animal (2626) 2626
stroke - etiology (2500) 2500
association (2416) 2416
heart (2415) 2415
blood pressure (2382) 2382
epidemiology (2379) 2379
medicine and health sciences (2326) 2326
cardiology (2320) 2320
case-control studies (2302) 2302
risk-factors (2284) 2284
hospitals (2281) 2281
prevalence (2256) 2256
proteins (2253) 2253
hematology (2238) 2238
heart diseases (2232) 2232
population (2220) 2220
stroke - epidemiology (2207) 2207
medicine, general & internal (2187) 2187
cell biology (2158) 2158
prevention (2148) 2148
diagnosis (2142) 2142
health risk assessment (2130) 2130
expression (2103) 2103
rodents (2079) 2079
adolescent (2073) 2073
age (2066) 2066
apoptosis (2042) 2042
mutation (2039) 2039
biochemistry & molecular biology (1994) 1994
genotype (1980) 1980
physiological aspects (1977) 1977
gene expression (1973) 1973
myocardial-infarction (1972) 1972
prognosis (1963) 1963
time factors (1957) 1957
heart attacks (1955) 1955
prospective studies (1943) 1943
treatment outcome (1936) 1936
genetic predisposition to disease (1893) 1893
surgery (1876) 1876
biology and life sciences (1875) 1875
abridged index medicus (1864) 1864
young adult (1861) 1861
stroke - pathology (1859) 1859
stroke - physiopathology (1851) 1851
cardiovascular (1814) 1814
medicine & public health (1788) 1788
physiology (1746) 1746
brain research (1733) 1733
stroke volume (1728) 1728
clinical trials (1711) 1711
brain - pathology (1708) 1708
usage (1677) 1677
cerebral infarction (1675) 1675
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (28) 28
Online Resources - Online (13) 13
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (10) 10
Collection Dvlpm't (Acquisitions) - Vendor file (9) 9
Baycrest Hospital - Stacks (3) 3
Providence Healthcare - Stacks (2) 2
St. Michael's Hospital - Stacks (2) 2
Providence Healthcare - Reference (1) 1
Scarborough Hospital - General (1) 1
UofT at Mississauga - Stacks (1) 1
West Park Healthcare Centre - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (45741) 45741
Japanese (147) 147
Portuguese (121) 121
Chinese (117) 117
Russian (112) 112
Spanish (100) 100
French (83) 83
German (79) 79
Norwegian (32) 32
Hungarian (18) 18
Polish (15) 15
Turkish (12) 12
Ukrainian (7) 7
Italian (6) 6
Korean (5) 5
Croatian (4) 4
Swedish (4) 4
Czech (3) 3
Dutch (3) 3
Finnish (3) 3
Hebrew (2) 2
Serbian (2) 2
Urdu (2) 2
Chamorro (1) 1
Danish (1) 1
Icelandic (1) 1
Lithuanian (1) 1
Persian (1) 1
Welsh (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Williams, Frances M. K and Carter, Angela M and Hysi, Pirro G and Surdulescu, Gabriela and Hodgkiss, Dylan and Soranzo, Nicole and Traylor, Matthew and Bevan, Steve and Dichgans, Martin and Rothwell, Peter M. W and Sudlow, Cathie and Farrall, Martin and Silander, Kaisa and Kaunisto, Mari and Wagner, Peter and Saarela, Olli and Kuulasmaa, Kari and Virtamo, Jarmo and Salomaa, Veikko and Amouyel, Philippe and Arveiler, Dominique and Ferrieres, Jean and Wiklund, Per-Gunnar and Arfan Ikram, M and Hofman, Albert and Boncoraglio, Giorgio B and Parati, Eugenio A and Helgadottir, Anna and Gretarsdottir, Solveig and Thorsteinsdottir, Unnur and Thorleifsson, Gudmar and Stefansson, Kari and Seshadri, Sudha and DeStefano, Anita and Gschwendtner, Andreas and Psaty, Bruce and Longstreth, Will and Mitchell, Braxton D and Cheng, Yu-Ching and Clarke, Robert and Ferrario, Marco and Bis, Joshua C and Levi, Christopher and Attia, John and Holliday, Elizabeth G and Scott, Rodney J and Fornage, Myriam and Sharma, Pankaj and Furie, Karen L and Rosand, Jonathan and Nalls, Mike and Meschia, James and Mosely, Thomas H and Evans, Alun and Palotie, Aarno and Markus, Hugh S and Grant, Peter J and Spector, Tim D and on Behalf of the EuroCLOT Investigators the Wellcome Trust Case Control Consortium 2 MOnica Risk, Genetics, Archiving and Monograph MetaStroke and the International Stroke Genetics Consortium and EuroCLOT Investigators and Wellcome Trust Case Control Consor and Int Stroke Genetics Consortium and MOnica Risk, Genetics, Archiving and Monograph and MetaStroke and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2
Annals of neurology, ISSN 0364-5134, 2013, Volume 73, Issue 1, pp. 16 - 31
Journal Article
Seminars in immunopathology, ISSN 1863-2300, 2011, Volume 34, Issue 1, pp. 43 - 62
The interaction of coagulation factors with the perivascular environment affects the development of disease in ways that extend beyond their traditional roles... 
Autoimmunity | Complement receptor 3 | Multiple sclerosis | Stroke | Alzheimer’s disease | Internal Medicine | Macrophages | Blood brain barrier | Inflammatory disease | Microglia | Biomedicine | Immunology | Rheumatoid arthritis | CD11b/CD18 | Atherosclerosis | Plasminogen | Anticoagulant therapy | Alzheimer's disease | ALZHEIMERS-DISEASE | IMMUNOLOGY | PATHOLOGY | GAMMA-C-DOMAIN | BINDING-SITE | CENTRAL-NERVOUS-SYSTEM | MULTIPLE-SCLEROSIS LESIONS | CRYSTAL-STRUCTURE | BLOOD-BRAIN-BARRIER | INTEGRIN ALPHA(M)BETA | PROTEASE-ACTIVATED RECEPTORS | PERIPHERAL ARTERIAL-DISEASE | Colitis - genetics | Humans | Brain Injuries - metabolism | Arthritis, Rheumatoid - metabolism | Bacterial Infections - genetics | Inflammation - metabolism | Blood Coagulation - immunology | Muscular Dystrophy, Duchenne - immunology | Alzheimer Disease - immunology | Fibrinogen - immunology | Thromboplastin - immunology | Pulmonary Fibrosis - immunology | Vascular Diseases - genetics | Brain Injuries - genetics | Thrombin - genetics | Kidney Diseases - immunology | Arthritis, Rheumatoid - genetics | Neoplasms - immunology | Colitis - metabolism | Muscular Dystrophy, Duchenne - genetics | Bacterial Infections - metabolism | Neoplasms - metabolism | Pulmonary Fibrosis - genetics | Spinal Cord Injuries - genetics | Kidney Diseases - genetics | Stroke - genetics | Brain Injuries - immunology | Neoplasms - genetics | Bacterial Infections - immunology | Pulmonary Fibrosis - metabolism | Colitis - immunology | Thrombin - immunology | Stroke - immunology | Kidney Diseases - metabolism | Multiple Sclerosis - metabolism | Vascular Diseases - immunology | Spinal Cord Injuries - metabolism | Multiple Sclerosis - genetics | Inflammation - immunology | Fibrinogen - genetics | Stroke - metabolism | Animals | Thromboplastin - genetics | Alzheimer Disease - metabolism | Fibrinogen - metabolism | Inflammation - genetics | Multiple Sclerosis - immunology | Blood Coagulation - genetics | Spinal Cord Injuries - immunology | Muscular Dystrophy, Duchenne - metabolism | Thrombin - metabolism | Thromboplastin - metabolism | Alzheimer Disease - genetics | Arthritis, Rheumatoid - immunology | Vascular Diseases - metabolism | Nervous system diseases | Bacterial infections | Oncology, Experimental | Thrombin | Inflammation | Anticoagulants (Medicine) | Research | Rheumatoid factor | Fibrin | Fibrinogen | Genetic research | Colitis | Cancer | Traumatic brain injury | Coagulation | Tissue factor | hemostasis | Spinal cord injury | Inflammatory diseases | Kidney | Signal transduction | Duchenne's muscular dystrophy | Neurodegenerative diseases | Therapeutic applications | Thrombosis | Coagulation factors | Infection | Molecular modelling | Fibrosis | Brain injury
Journal Article
PloS one, ISSN 1932-6203, 2011, Volume 6, Issue 7, p. e22542
Background: Moyamoya disease is an idiopathic vascular disorder of intracranial arteries. Its susceptibility locus has been mapped to 17q25.3 in Japanese... 
MIDDLE CEREBRAL-ARTERY | WILLIS | VIRUS-INFECTION | ZEBRAFISH | SPONTANEOUS OCCLUSION | BIOLOGY | FIBROBLAST-GROWTH-FACTOR | LINKAGE ANALYSIS | CEREBROSPINAL-FLUID | EXPRESSION | CIRCLE | Moyamoya Disease - ethnology | Blood Vessels - metabolism | Humans | DNA, Complementary - genetics | 3' Untranslated Regions - genetics | Molecular Sequence Data | Male | Case-Control Studies | Gene Knockdown Techniques | Blood Vessels - physiopathology | Base Sequence | Cloning, Molecular | HEK293 Cells | Adult | Female | Genetic Predisposition to Disease - genetics | Gene Expression Regulation | Ubiquitin-Protein Ligases - metabolism | Linkage Disequilibrium - genetics | Exons - genetics | Zebrafish | DNA Copy Number Variations - genetics | Open Reading Frames - genetics | Sequence Homology, Amino Acid | Exome - genetics | Animals | Adenosine Triphosphatases | Alleles | Ubiquitin-Protein Ligases - deficiency | Moyamoya Disease - physiopathology | HeLa Cells | Ubiquitin-Protein Ligases - genetics | Moyamoya Disease - genetics | Ubiquitin | Medical colleges | Disease susceptibility | Genetic aspects | Gene mutations | Genes | Haplotypes | Transcription | Laboratories | Genomics | Chicken pox | Infections | Single-nucleotide polymorphism | Family medical history | Neurosurgery | Carotid arteries | Arteries | Ubiquitination | Life sciences | Informatics | Ubiquitin-protein ligase | Linkage analysis | Lupus | Hypertension | Cytomegalovirus | Stroke | Moyamoya disease | Cytokines | Susceptibility | Blood vessels | Radiation therapy | Disease control | Patients | Loci | Studies | Environmental science | Genotyping | Mutation | Gene mapping | Adenosine triphosphatase | Veins & arteries
Journal Article
by Helgadottir, Anna and Gretarsdottir, Solveig and Thorleifsson, Gudmar and Holm, Hilma and Patel, Riyaz S and Gudnason, Thorarinn and Jones, Gregory T and van Rij, Andre M and Eapen, Danny J and Baas, Annette F and Tregouet, David-Alexandre and Morange, Pierre-Emmanuel and Emmerich, Joseph and Lindblad, Bengt and Gottsäter, Anders and Kiemeny, Lambertus A and Lindholt, Jes S and Sakalihasan, Natzi and Ferrell, Robert E and Carey, David J and Elmore, James R and Tsao, Philip S and Grarup, Niels and Jørgensen, Torben and Witte, Daniel R and Hansen, Torben and Pedersen, Oluf and Pola, Roberto and Gaetani, Eleonora and Magnadottir, Hulda B and Wijmenga, Cisca and Tromp, Gerard and Ronkainen, Antti and Ruigrok, Ynte M and Blankensteijn, Jan D and Mueller, Thomas and Wells, Philip S and Corral, Javier and Soria, Jose Manuel and Souto, Juan Carlos and Peden, John F and Jalilzadeh, Shapour and Mayosi, Bongani M and Keavney, Bernard and Strawbridge, Rona J and Sabater-Lleal, Maria and Gertow, Karl and Baldassarre, Damiano and Nyyssönen, Kristiina and Rauramaa, Rainer and Smit, Andries J and Mannarino, Elmo and Giral, Philippe and Tremoli, Elena and de Faire, Ulf and Humphries, Steve E and Hamsten, Anders and Haraldsdottir, Vilhelmina and Olafsson, Isleifur and Magnusson, Magnus K and Samani, Nilesh J and Levey, Allan I and Markus, Hugh S and Kostulas, Konstantinos and Dichgans, Martin and Berger, Klaus and Kuhlenbäumer, Gregor and Ringelstein, E. Bernd and Stoll, Monika and Seedorf, Udo and Rothwell, Peter M and Powell, Janet T and Kuivaniemi, Helena and Onundarson, Pall T and Valdimarsson, Einar and Matthiasson, Stefan E and Gudbjartsson, Daniel F and Thorgeirsson, Guðmundur and Quyyumi, Arshed A and Watkins, Hugh and Farrall, Martin and Thorsteinsdottir, Unnur and Stefansson, Kari
Journal of the American College of Cardiology, ISSN 0735-1097, 2012, Volume 60, Issue 8, pp. 722 - 729
Objectives The purpose of this study is investigate the effects of variants in the apolipoprotein(a) gene ( LPA ) on vascular diseases with different... 
Cardiovascular | Internal Medicine | atherosclerosis | genetic | association | thrombosis | lipoprotein(a) | INTIMA-MEDIA THICKNESS | RISK-FACTORS | METAANALYSIS | MYOCARDIAL-INFARCTION | UMCG Approved | VASCULAR-DISEASE | WOMEN | PERIPHERAL ARTERIAL-DISEASE | ISCHEMIC-STROKE | SEVERITY | CARDIAC & CARDIOVASCULAR SYSTEMS | Severity of Illness Index | Myocardial Infarction - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Apolipoproteins A - genetics | Angiography | Carotid Intima-Media Thickness | Intracranial Aneurysm - genetics | Atherosclerosis - genetics | Humans | Risk Factors | Brain Ischemia - genetics | African Americans - genetics | Linear Models | Logistic Models | Aortic Aneurysm, Abdominal - genetics | Stroke - genetics | Venous Thromboembolism - genetics | Peripheral Arterial Disease - genetics | Age of Onset | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Medical colleges | Neurosciences | Stock options | Genes | Aneurysms | Coronary heart disease | Biometry | Lipoprotein A | Anopheles | Atherosclerosis | Medical genetics | Genetic research | Genetic aspects | Diabetes | Thromboembolism | Cardiology | Public health | Dementia | Stroke | Medical imaging | Values | Cardiovascular disease | Apolipoproteins | Thrombosis | Studies | Confidence intervals | Coronary vessels | Blood pressure | Drug therapy | Age | Methods | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
PLoS genetics, ISSN 1553-7404, 2016, Volume 12, Issue 10, p. e1006367
Journal Article
PLoS genetics, ISSN 1553-7404, 2016, Volume 12, Issue 11, p. e1006314
Journal Article
PloS one, ISSN 1932-6203, 10/2017, Volume 12, Issue 10, p. e0185785
Background Hereditary thrombophilia (HT) is a genetic predisposition to thrombosis... 
POPULATION | FACTOR-V-LEIDEN | RISK-FACTORS | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | PULMONARY-EMBOLISM | MUTATION | DEEP-VEIN THROMBOSIS | ANTITHROMBIN-III | PROTEIN-C | CARRIERS | Protein C Deficiency - complications | Conjunctivitis - genetics | Protein C Deficiency - physiopathology | Humans | Middle Aged | Plasminogen - genetics | Male | Antithrombin III Deficiency - genetics | Antithrombin III - genetics | Skin Diseases, Genetic - genetics | Thrombophilia - etiology | Protein S Deficiency - genetics | Thrombophilia - diagnosis | Antithrombin III Deficiency - physiopathology | Skin Diseases, Genetic - diagnosis | Adult | Female | Retrospective Studies | Antithrombin III Deficiency - complications | Protein S Deficiency - physiopathology | Skin Diseases, Genetic - complications | Antithrombin III Deficiency - diagnosis | Republic of Korea | Venous Thromboembolism - diagnosis | Thrombophilia - genetics | Gene Expression | Protein S Deficiency - complications | Protein S - genetics | Thrombophilia - physiopathology | Sequence Analysis, DNA | Venous Thromboembolism - etiology | Venous Thromboembolism - genetics | Skin Diseases, Genetic - physiopathology | Venous Thromboembolism - physiopathology | Conjunctivitis - physiopathology | Protein C Deficiency - diagnosis | Aged | Protein C Deficiency - genetics | Conjunctivitis - complications | Protein C - genetics | Protein S Deficiency - diagnosis | Conjunctivitis - diagnosis | Plasminogen - deficiency | Type 2 diabetes | Protein C | Genetic aspects | Research | Nucleotide sequencing | Health aspects | DNA sequencing | Hypertension | Anticoagulants | Stroke | Laboratories | Embolisms | Protein deficiency | Antithrombin | Patients | Thrombosis | Gene sequencing | Proteins | Medicine | Thrombophilia | Protein S | Genetics | Diabetes | Mutation | Thromboembolism | Cardiology | Health risk assessment | Deoxyribonucleic acid--DNA | Veins & arteries | Deoxyribonucleic acid | DNA
Journal Article