X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1232) 1232
Publication (157) 157
Book / eBook (145) 145
Book Chapter (42) 42
Book Review (34) 34
Newsletter (9) 9
Conference Proceeding (2) 2
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (904) 904
index medicus (631) 631
female (409) 409
male (396) 396
genetic aspects (299) 299
mutation (273) 273
adult (272) 272
animals (257) 257
neurosciences (236) 236
middle aged (234) 234
research (227) 227
clinical neurology (224) 224
genetics (199) 199
multiple sclerosis (166) 166
risk factors (161) 161
amyotrophic lateral sclerosis (154) 154
disease (153) 153
amyotrophic-lateral-sclerosis (149) 149
familial als (136) 136
aged (135) 135
familial mediterranean fever (132) 132
diagnosis (119) 119
mice (116) 116
genetics & heredity (112) 112
neurology (112) 112
medicine (107) 107
genetic predisposition to disease (105) 105
child (104) 104
health aspects (103) 103
pathology (103) 103
review (103) 103
multiple-sclerosis (99) 99
nervous system (99) 99
proteins (99) 99
diseases (97) 97
adolescent (96) 96
alzheimer's disease (94) 94
care and treatment (92) 92
familial alzheimers-disease (91) 91
article (90) 90
biochemistry & molecular biology (89) 89
nervous system diseases (88) 88
physiological aspects (87) 87
research article (87) 87
pedigree (85) 85
analysis (83) 83
amyotrophic lateral sclerosis - genetics (80) 80
disease models, animal (79) 79
development and progression (77) 77
patients (77) 77
disease progression (76) 76
dementia (74) 74
inflammation (73) 73
multiple sclerosis - genetics (73) 73
rheumatology (73) 73
multidisciplinary sciences (71) 71
immunology (70) 70
neurodegeneration (70) 70
neurodegenerative diseases (70) 70
genes (69) 69
cancer (67) 67
medicine, research & experimental (67) 67
mutations (67) 67
superoxide dismutase - genetics (67) 67
young adult (67) 67
gene (66) 66
prevalence (66) 66
magnetic resonance imaging (65) 65
familial & genetic (64) 64
epidemiology (63) 63
age (62) 62
cell biology (62) 62
gene expression (61) 61
medical research (61) 61
pediatrics (59) 59
phenotype (59) 59
child, preschool (58) 58
case-control studies (57) 57
children (57) 57
medicine, general & internal (57) 57
neurons (57) 57
pharmacology & pharmacy (57) 57
brain - pathology (56) 56
degeneration (55) 55
rodents (55) 55
familial aggregation (54) 54
pathogenesis (53) 53
studies (53) 53
superoxide dismutase-1 (53) 53
amyotrophic lateral sclerosis - pathology (52) 52
brain (52) 52
psychiatry (52) 52
gene mutations (51) 51
science (51) 51
alzheimer disease (50) 50
genotype (50) 50
mice, transgenic (50) 50
motor-neuron disease (48) 48
mutation - genetics (48) 48
risk (48) 48
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (109) 109
Providence Healthcare - Stacks (12) 12
Robarts - Stacks (10) 10
Baycrest Hospital - Stacks (9) 9
UTL at Downsview - May be requested (9) 9
Online Resources - Online (8) 8
UofT at Scarborough - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Vendor file (4) 4
OISE - Stacks (4) 4
UofT at Mississauga - Stacks (4) 4
Baycrest Hospital - Wellness Library (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Law (Bora Laskin) - Stacks (2) 2
Stacks (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Baycrest Hospital - Missing (1) 1
Bridgepoint Health - Stacks (1) 1
Criminology - Stacks (1) 1
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Humber River Regional Hospital - Church Stacks (1) 1
Patient Education (1) 1
Providence Healthcare - Reference (1) 1
Robarts - Course Reserves (1) 1
Scarborough Hospital - General (1) 1
St. Michael's Hospital - Stacks (1) 1
West Park Healthcare Centre - Hospital Department (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 (1392) 1392
Spanish (15) 15
French (12) 12
German (10) 10
Japanese (5) 5
Dutch (2) 2
Italian (1) 1
Polish (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Medical Hypotheses, ISSN 0306-9877, 10/2019, Volume 131, p. 109310
Multiple Sclerosis (MS) is a demyelinating CNS disease. Most MS cases are sporadic, however about 20 percent of them are hereditary (Ramagopalan and Sadovnick,... 
Multiple sclerosis | MSSS | Familial cases | MRI | EDSS | MEDICINE, RESEARCH & EXPERIMENTAL | TRANSMISSION | ORIGIN | MS | PARENT | RISK | EPIDEMIOLOGY
Journal Article
Acta Neurologica Scandinavica, ISSN 0001-6314, 03/2019, Volume 139, Issue 3, pp. 231 - 237
Objectives The overall distribution of disease courses in multiple sclerosis (MS) is well established, but little is known about the distribution among... 
MS courses | multiple sclerosis | progressive MS | relapse‐remitting MS | familial MS | relapse-remitting MS | DIFFERENTIAL-DIAGNOSIS | BOUT-ONSET | RISK | RELIABILITY | NATURAL-HISTORY | CONCORDANCE | CLINICAL NEUROLOGY | SIBLING PAIRS | AGE | Family | Study and teaching | Multiple sclerosis | Genetic aspects | Analysis | Data processing | Statistical analysis | Diagnosis | Health risk assessment | Age
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 2013, Volume 84, Issue 1, pp. 79 - 87
Journal Article
Immunogenetics, ISSN 0093-7711, 3/2018, Volume 70, Issue 3, pp. 205 - 207
The implementation of exome sequencing technologies has started to unravel the genetic etiology of familial multiple sclerosis (MS). A homozygote p.G587S... 
Human Genetics | Gene Function | Allergology | NOD-like receptors | Multiple sclerosis | Biomedicine | Immunology | Familial | Mutation | NLRP1 | Cell Biology | INFLAMMASOME ACTIVATION | DISEASE | GENETICS & HEREDITY | RISK | IMMUNOLOGY | DIAGNOSTIC-CRITERIA | Development and progression | Segregation | Melanoma | Medical genetics | Etiology | Patients | Gene sequencing
Journal Article
Journal of Neuroimmunology, ISSN 0165-5728, 05/2019, Volume 330, pp. 74 - 80
The HLA-DR15 extended haplotype comprises the strongest genetic risk factor for multiple sclerosis (MS). The aim of this work was to investigate whether... 
HLA-DR15 | Multiple sclerosis | Brazilians | Susceptibility | Familial | HLA-DRB1 | RISK | MHC | POLYMORPHISM | IMMUNOLOGY | NEUROSCIENCES | DISABILITY | HLA-DR LOCUS | CLASS-II ALLELES | LINKAGE | ASSOCIATION | Histocompatibility antigens | HLA histocompatibility antigens | Disease susceptibility | Genetic aspects | Molecular biology | Risk factors
Journal Article
Journal of Neurology, ISSN 0340-5354, 02/2019, Volume 266, Issue 2, pp. 481 - 486
BackgroundPersons who develop multiple sclerosis (MS) at a young age may bear a higher genetic risk load than persons who develop MS later in life; however,... 
Genetics | Multiple sclerosis | Early onset | Familial risk | Late onset | POPULATION | GENETIC RISK | CLINICAL NEUROLOGY | AGE | Genetic aspects | Genetic susceptibility | Familial diseases | Risk factors | Health risk assessment | Age | Original Communication
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 01/2018, Volume 22, Issue 1, pp. 72 - 81
To investigate frequency and phenotype of and mutations in childhood-onset multiple sclerosis (MS). Twenty-nine clinically well characterized patients were... 
Multiple sclerosis | Familial Mediterranean fever | TRAPS | FMF | Tumor necrosis factor receptor 1-associated periodic syndrome | Childhood | R92Q | VARIANTS | RISK | MEDITERRANEAN FEVER GENE | PERIODIC-SYNDROME | CLINICAL NEUROLOGY | COMMON MUTATIONS | DEMYELINATION | PEDIATRICS
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2014, Volume 346, Issue 1, pp. 268 - 270
Journal Article