X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1780) 1780
Publication (158) 158
Book / eBook (148) 148
Book Chapter (56) 56
Book Review (46) 46
Newsletter (43) 43
Newspaper Article (15) 15
Dissertation (5) 5
Conference Proceeding (4) 4
Magazine Article (3) 3
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
epilepsy (1408) 1408
humans (1360) 1360
clinical neurology (1032) 1032
index medicus (859) 859
child (810) 810
male (742) 742
female (725) 725
electroencephalography (592) 592
seizures (592) 592
child, preschool (490) 490
adolescent (487) 487
children (473) 473
neurosciences (400) 400
neurology (380) 380
pediatrics (337) 337
adult (293) 293
infant (273) 273
epilepsy - physiopathology (241) 241
epilepsy - diagnosis (235) 235
eeg (222) 222
rolandic epilepsy (212) 212
anticonvulsants - therapeutic use (210) 210
magnetic resonance imaging (209) 209
epilepsy - genetics (191) 191
sleep (180) 180
mutation (179) 179
genetics (177) 177
childhood (172) 172
brain (167) 167
analysis (160) 160
prognosis (159) 159
diagnosis (155) 155
temporal-lobe epilepsy (141) 141
syndrome (137) 137
risk factors (135) 135
epilepsy - drug therapy (132) 132
animals (131) 131
brain - physiopathology (129) 129
psychiatry (129) 129
genetic aspects (128) 128
research (128) 128
epilepsy - complications (120) 120
retrospective studies (116) 116
young adult (115) 115
infant, newborn (112) 112
classification (111) 111
convulsions & seizures (111) 111
epilepsy, rolandic - physiopathology (111) 111
epilepsy - epidemiology (110) 110
age of onset (107) 107
childhood epilepsy (107) 107
medicine & public health (107) 107
epilepsies, partial - physiopathology (106) 106
middle aged (106) 106
phenotype (106) 106
centrotemporal spikes (105) 105
surgery (105) 105
juvenile myoclonic epilepsy (103) 103
epilepsy - etiology (102) 102
article (100) 100
medical research (99) 99
comorbidity (98) 98
epilepsy, rolandic - diagnosis (98) 98
genes (98) 98
genetics & heredity (98) 98
age factors (96) 96
epilepsies, partial - diagnosis (95) 95
neuropsychological tests (94) 94
pedigree (94) 94
epilepsy - classification (91) 91
neuroimaging (91) 91
diagnosis, differential (90) 90
follow-up studies (88) 88
electroencephalography - methods (87) 87
mutations (86) 86
idiopathic generalized epilepsy (85) 85
antiepileptic drugs (84) 84
cerebral cortex - physiopathology (84) 84
behavioral sciences (83) 83
treatment outcome (83) 83
epilepsy in children (82) 82
seizures - physiopathology (82) 82
studies (82) 82
sleep - physiology (79) 79
benign childhood epilepsy (76) 76
care and treatment (76) 76
medicine, experimental (76) 76
patients (76) 76
epilepsies, partial - genetics (75) 75
etiology (75) 75
anticonvulsants (74) 74
age (72) 72
autism (72) 72
epilepsy, rolandic - genetics (71) 71
frontal-lobe epilepsy (71) 71
encephalopathy (70) 70
prevalence (70) 70
cognition (68) 68
medicine (68) 68
cortex (67) 67
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (116) 116
Collection Dvlpm't (Acquisitions) - Closed Orders (8) 8
Collection Dvlpm't (Acquisitions) - Vendor file (5) 5
Holland Bloorview Kids Rehabilitation - Stacks (5) 5
Online Resources - Online (3) 3
Credit Valley Hospital - Stacks (1) 1
Gerstein Science - Circulation Desk (1) 1
Scarborough Hospital - General (1) 1
Stacks (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1991) 1991
French (12) 12
Spanish (12) 12
German (11) 11
Portuguese (4) 4
Russian (4) 4
Croatian (1) 1
Czech (1) 1
Danish (1) 1
Italian (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Molecular Genetics, ISSN 0964-6906, 11/2014, Volume 23, Issue 22, pp. 6069 - 6080
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2018, Volume 13, Issue 8, p. e0202022
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2009, Volume 17, Issue 9, pp. 1171 - 1181
Journal Article
Journal Article
Epilepsia, ISSN 0013-9580, 12/2007, Volume 48, Issue 12, pp. 2258 - 2265
Summary Purpose: Associations between rolandic epilepsy (RE) with reading disability (RD) and speech sound disorder (SSD) have not been tested in a controlled... 
Developmental dyslexia | Phonologic disorder | Articulation disorder | Centrotemporal sharp waves | Comorbidity | Family study | Complex genetic | Speech delay | Developmental dysphasia | Cognitive deficit | Familial aggregation | cognitive deficit | centrotemporal sharp waves | articulation disorder | complex genetic | developmental dyslexia | familial aggregation | PREVALENCE | CHILDHOOD | CLINICAL NEUROLOGY | phonologic disorder | CHILDREN | IMPAIRMENT | family study | comorbidity | GENETICS | BENIGN EPILEPSY | speech delay | developmental dysphasia | LANGUAGE DISORDERS | Aphasia, Wernicke - genetics | Genetic Testing | Prevalence | Aphasia, Wernicke - epidemiology | Epilepsy, Rolandic - genetics | Humans | Child, Preschool | Male | Case-Control Studies | Dyslexia - epidemiology | Epilepsy, Rolandic - diagnosis | Language Development Disorders - epidemiology | Language Development Disorders - diagnosis | Epilepsy, Rolandic - epidemiology | Phonetics | Adult | Female | Surveys and Questionnaires | Functional Laterality - physiology | Child | Aphasia, Wernicke - diagnosis | Dyslexia - diagnosis | International Classification of Diseases | Genetic Predisposition to Disease - genetics | Language Development Disorders - genetics | Risk Factors | Dyslexia - genetics | Adolescent | Family | Medicine, Experimental | Medical research | Epilepsy
Journal Article
Epilepsia, ISSN 0013-9580, 2010, Volume 51, Issue 9, pp. 1870 - 1873
Journal Article