X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1007) 1007
index medicus (789) 789
female (647) 647
male (585) 585
clinical neurology (516) 516
malformations (414) 414
child (404) 404
epilepsy (367) 367
adult (345) 345
magnetic resonance imaging (333) 333
adolescent (324) 324
surgery (308) 308
child, preschool (301) 301
neurosciences (301) 301
infant (251) 251
brain (239) 239
abnormalities (226) 226
dysplasia (225) 225
children (207) 207
neurology (203) 203
pediatrics (203) 203
middle aged (202) 202
focal cortical dysplasia (181) 181
seizures (178) 178
young adult (168) 168
medicine & public health (166) 166
retrospective studies (166) 166
classification (164) 164
animals (147) 147
diagnosis (144) 144
treatment outcome (143) 143
genetics & heredity (132) 132
infant, newborn (132) 132
brain - pathology (131) 131
malformations of cortical development - pathology (127) 127
neurosurgery (125) 125
radiology, nuclear medicine & medical imaging (119) 119
pregnancy (118) 118
neuroimaging (116) 116
pathology (116) 116
magnetic resonance imaging - methods (113) 113
electroencephalography (111) 111
epilepsy - pathology (109) 109
research (106) 106
temporal-lobe epilepsy (103) 103
cortex (102) 102
mutation (100) 100
genetic aspects (98) 98
mri (98) 98
analysis (95) 95
cerebral cortex - pathology (92) 92
care and treatment (89) 89
article (88) 88
aged (83) 83
genetics (83) 83
epilepsy - etiology (82) 82
epilepsy surgery (82) 82
follow-up studies (80) 80
phenotype (80) 80
epilepsy - surgery (79) 79
malformations of cortical development - complications (79) 79
risk factors (79) 79
cerebral cortex - abnormalities (78) 78
diseases (78) 78
fetus (78) 78
malformations of cortical development - diagnosis (76) 76
health aspects (74) 74
neurons (72) 72
features (70) 70
syndrome (70) 70
brain - abnormalities (68) 68
epilepsy - diagnosis (66) 66
malformations of cortical development - surgery (64) 64
intractable epilepsy (63) 63
medicine (63) 63
natural-history (61) 61
neuroradiology (61) 61
genetic disorders (59) 59
mutations (58) 58
diagnosis, differential (57) 57
patients (57) 57
cortical dysplasia (56) 56
management (56) 56
polymicrogyria (56) 56
congenital abnormalities (55) 55
neuronal migration (54) 54
abnormalities, human (53) 53
cortical development (53) 53
diagnostic imaging (53) 53
malformations of cortical development (53) 53
nervous system (53) 53
prognosis (53) 53
tuberous sclerosis complex (53) 53
nervous system malformations - pathology (52) 52
eeg (50) 50
epilepsy - physiopathology (50) 50
immunohistochemistry (50) 50
radiography (50) 50
expression (49) 49
ultrasound (49) 49
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (134) 134
UTL at Downsview - May be requested (19) 19
Dentistry (Harry R Abbott) - Stacks (8) 8
Holland Bloorview Kids Rehabilitation - Stacks (8) 8
UofT at Mississauga - Stacks (8) 8
Dentistry (Harry R Abbott) - Withdrawn (6) 6
Collection Dvlpm't (Acquisitions) - Closed Orders (5) 5
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (4) 4
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Earth Sciences (Noranda) - Stacks (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Online Resources - Online (2) 2
Scarborough Hospital - General (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Credit Valley Hospital - Reserve desk (1) 1
Credit Valley Hospital - Stacks (1) 1
Gerstein Science - Missing (1) 1
Holland Bloorview Kids Rehabilitation - Reference (1) 1
Humber River Regional Hospital - Church Stacks (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Scarborough Hospital - Birchmount (1) 1
St Josephs Health Centre - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's Hospital - Stacks (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UofT at Scarborough - May be requested in 6-10 wks (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1356) 1356
Spanish (6) 6
French (3) 3
German (3) 3
Portuguese (3) 3
Japanese (2) 2
Russian (2) 2
Turkish (2) 2
Arabic (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European Journal of Human Genetics, ISSN 1018-4813, 04/2013, Volume 21, Issue 4, pp. 381 - 385
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2012, Volume 20, Issue 10, pp. 1024 - 1031
We present six patients from five unrelated families with a condition originally described by Van Maldergem et al and provide follow-up studies of the original... 
blepharo-naso-facial malformation | choanal atresia | camptodactyly | autosomal recessive | migration abnormalities | bilateral periventricular nodular heterotopia | PACHYGYRIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | MALFORMATIONS | PERIVENTRICULAR HETEROTOPIA | GENETICS & HEREDITY | FACIAL ABNORMALITIES | JOINT CONTRACTURES | MUTATIONS | Abnormalities, Multiple - pathology | Malformations of Cortical Development, Group II - pathology | Humans | Joint Instability - genetics | Child, Preschool | Joint Instability - pathology | Foot Deformities, Congenital - genetics | Male | Hand Deformities, Congenital - diagnosis | Intellectual Disability - genetics | Craniofacial Abnormalities - pathology | Female | Child | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Foot Deformities, Congenital - pathology | Diagnosis, Differential | Joint Instability - diagnosis | Intellectual Disability - pathology | Malformations of Cortical Development, Group II - diagnosis | Foot Deformities, Congenital - diagnosis | Malformations of Cortical Development, Group II - genetics | Genes, Recessive | Craniofacial Abnormalities - diagnosis | Hand Deformities, Congenital - genetics | Pedigree | Abnormalities, Multiple - diagnosis | Intellectual Disability - diagnosis | Consanguinity | Hand Deformities, Congenital - pathology | Karyotype | Hypoplasia | Neonates | Phenotypes | Leukocyte migration | Intellectual disabilities | Childrens health | Heredity | Blepharophimosis | Patients | Maxilla | Feeding | Genotype & phenotype | Parents & parenting | Ostomy | Hospitals | Genetics | Mutation | Microtia | Cell migration | Mental retardation | Siblings
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e73144
Journal Article
Journal Article