X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (39097) 39097
Book Review (7049) 7049
Newsletter (5231) 5231
Publication (3572) 3572
Newspaper Article (2613) 2613
Book Chapter (557) 557
Conference Proceeding (398) 398
Book / eBook (338) 338
Magazine Article (151) 151
Trade Publication Article (90) 90
Dissertation (69) 69
Government Document (68) 68
Web Resource (68) 68
Reference (17) 17
Transcript (11) 11
Report (8) 8
Data Set (6) 6
Streaming Video (6) 6
Paper (5) 5
Journal / eJournal (3) 3
Presentation (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
epilepsy (34585) 34585
index medicus (29428) 29428
humans (22951) 22951
male (15179) 15179
female (13382) 13382
clinical neurology (12681) 12681
seizures (11641) 11641
neurosciences (10563) 10563
animals (10119) 10119
adult (7100) 7100
child (7017) 7017
neurology (6479) 6479
research (6234) 6234
adolescent (5934) 5934
electroencephalography (5403) 5403
epilepsy - genetics (4878) 4878
analysis (4861) 4861
brain (4853) 4853
genetic aspects (4787) 4787
child, preschool (4712) 4712
mutation (4687) 4687
rats (3968) 3968
mice (3834) 3834
temporal-lobe epilepsy (3819) 3819
pediatrics (3812) 3812
middle aged (3792) 3792
children (3670) 3670
infant (3575) 3575
anticonvulsants - therapeutic use (3199) 3199
epilepsy - physiopathology (3172) 3172
medical research (3147) 3147
epilepsy - drug therapy (3008) 3008
disease models, animal (2910) 2910
magnetic resonance imaging (2829) 2829
neurons (2797) 2797
genetics & heredity (2757) 2757
young adult (2541) 2541
medicine, experimental (2515) 2515
psychiatry (2478) 2478
genetics (2400) 2400
convulsions & seizures (2363) 2363
article (2336) 2336
phenotype (2334) 2334
genetic research (2314) 2314
reports (2313) 2313
risk factors (2284) 2284
hippocampus (2173) 2173
genes (2104) 2104
nervous system (2052) 2052
antiepileptic drugs (1980) 1980
care and treatment (1939) 1939
epilepsy - diagnosis (1892) 1892
diagnosis (1881) 1881
health aspects (1872) 1872
anticonvulsants (1856) 1856
eeg (1832) 1832
pharmacology & pharmacy (1768) 1768
aged (1737) 1737
pedigree (1725) 1725
biochemistry & molecular biology (1724) 1724
studies (1680) 1680
epilepsy - etiology (1665) 1665
medicine (1665) 1665
patients (1654) 1654
status epilepticus (1654) 1654
proteins (1651) 1651
mutations (1615) 1615
autism (1602) 1602
drug therapy (1599) 1599
universities and colleges (1568) 1568
abridged index medicus (1558) 1558
multidisciplinary sciences (1546) 1546
infant, newborn (1535) 1535
brain - physiopathology (1528) 1528
physiological aspects (1518) 1518
brain - pathology (1508) 1508
gene (1506) 1506
gaba (1486) 1486
epilepsy - complications (1467) 1467
epilepsy - metabolism (1464) 1464
gene expression (1450) 1450
expression (1449) 1449
rodents (1443) 1443
seizures - physiopathology (1439) 1439
neuroimaging (1436) 1436
surgery (1431) 1431
epilepsy - pathology (1395) 1395
seizure (1390) 1390
cortex (1373) 1373
retrospective studies (1362) 1362
research article (1350) 1350
behavioral sciences (1332) 1332
disease (1306) 1306
epilepsy - epidemiology (1304) 1304
pregnancy (1290) 1290
syndrome (1267) 1267
anticonvulsants - adverse effects (1261) 1261
treatment outcome (1253) 1253
rats, sprague-dawley (1222) 1222
age (1217) 1217
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (217) 217
Online Resources - Online (26) 26
Collection Dvlpm't (Acquisitions) - Vendor file (20) 20
Holland Bloorview Kids Rehabilitation - Stacks (10) 10
Collection Dvlpm't (Acquisitions) - Closed Orders (9) 9
UTL at Downsview - May be requested (7) 7
UofT at Mississauga - Stacks (5) 5
OISE - Stacks (4) 4
Robarts - Stacks (2) 2
Scarborough Hospital - Online (2) 2
Stacks (2) 2
Thomas Fisher Rare Book - Rare Book (2) 2
Credit Valley Hospital - Online (1) 1
Credit Valley Hospital - Stacks (1) 1
Gerstein Science - Circulation Desk (1) 1
New College (Ivey) - Stacks (1) 1
Providence Healthcare - Stacks (1) 1
Scarborough Hospital - General (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's Hospital - Stacks (1) 1
Sunnybrook Health Sciences Centre - Online (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (46412) 46412
French (354) 354
Spanish (296) 296
German (286) 286
Russian (259) 259
Japanese (186) 186
Chinese (176) 176
Italian (72) 72
Polish (65) 65
Portuguese (55) 55
Hungarian (26) 26
Danish (24) 24
Czech (19) 19
Turkish (19) 19
Swedish (11) 11
Dutch (10) 10
Norwegian (10) 10
Romanian (10) 10
Croatian (9) 9
Finnish (9) 9
Korean (5) 5
Hebrew (4) 4
Slovak (3) 3
Ukrainian (3) 3
Bosnian (2) 2
Persian (2) 2
Slovenian (2) 2
Arabic (1) 1
Bulgarian (1) 1
Greek (1) 1
Hindi (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, pp. e28936 - e28936
The Clinic for Special Children (CSC) has integrated biochemical and molecular methods into a rural pediatric practice serving Old Order Amish and Mennonite... 
DOMAIN | POSTERIOR COLUMN ATAXIA | INTERACTING PROTEIN | MULTIDISCIPLINARY SCIENCES | C-MYC | SNIP1 | DEATH | TRANSFER-RNA | MUTATIONS | IDENTIFICATION | DISCOVERY | Seizures - genetics | Microtubule-Associated Proteins - genetics | CRADD Signaling Adaptor Protein | Humans | Child, Preschool | Infant | Amino Acyl-tRNA Synthetases | Receptors, Virus - genetics | Intellectual Disability - genetics | Amish - genetics | Ethnic Groups - genetics | Usher Syndromes - genetics | Membrane Transport Proteins - genetics | Chromosome Mapping - methods | Epilepsy - genetics | Parkinsonian Disorders - genetics | Nuclear Proteins - genetics | Child | Intracellular Signaling Peptides and Proteins - genetics | Infant, Newborn | Genetic Predisposition to Disease - genetics | Genetic Association Studies - methods | Dopamine Plasma Membrane Transport Proteins - genetics | Exome - genetics | Polymorphism, Single Nucleotide | Sequence Analysis, DNA - methods | Genetic aspects | Nucleotide sequencing | Single nucleotide polymorphisms | DNA sequencing | Neurosciences | Disease | Genes | Business improvement districts | Mapping | Biology | Single-nucleotide polymorphism | Gene polymorphism | Population genetics | Data bases | Gene sequencing | Coupling (molecular) | Enterprise zones | Lists | Children | Pathogens | Nuclear electric power generation | Pathogenicity | Medicine | Hospitals | DNA microarrays | Genotyping | Mutation | Gene mapping | Polymorphism | Index Medicus
Journal Article
Nature Communications, ISSN 2041-1723, 11/2015, Volume 6, Issue 1, pp. 8804 - 8804
textabstractEczema often precedes the development of asthma in a disease course called the a 'atopic march'. To unravel the genes underlying this... 
CHROMOSOME 11Q13 | JUVENILE MYOCLONIC EPILEPSY | DERMATITIS | FOOD ALLERGY | GENOMEWIDE ASSOCIATION | MULTIDISCIPLINARY SCIENCES | RISK | FILAGGRIN MUTATIONS | BIRTH COHORT | HAY-FEVER | CHILDHOOD ASTHMA | Phenotypes | Interleukin 4 | Eczema | Chromosome 6 | Skin diseases | Chromosome 12 | Allergic diseases | Genomes | Children | Loci | Asthma | Atopy | Index Medicus
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2009, Volume 5, Issue 9, pp. e1000649 - e1000649
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2018, Volume 115, Issue 28, pp. E6640 - E6649
Endosomes have emerged as a central hub and pathogenic driver of Alzheimer's disease (AD). The earliest brain cytopathology in neurodegeneration, occurring... 
Histone deacetylase | Trichostatin A | Amyloid beta | ApoE4 | exchanger | Na+/H+ exchanger | CHRISTIANSON SYNDROME | HUMAN BRAIN | trichostatin A | MULTIDISCIPLINARY SCIENCES | SPORADIC ALZHEIMERS-DISEASE | histone deacetylase | SYNAPTIC PLASTICITY | amyloid beta | APOLIPOPROTEIN-E | LYSOSOMAL DYSFUNCTION | DOWN-SYNDROME | A-BETA | GENE-EXPRESSION | PRECURSOR PROTEIN | Microcephaly - genetics | Epigenesis, Genetic | Humans | Astrocytes - pathology | Epilepsy - metabolism | Endosomes - metabolism | Alzheimer Disease - pathology | Intellectual Disability - metabolism | Amyloid beta-Peptides - genetics | Amyloid beta-Peptides - metabolism | Ataxia - drug therapy | Genetic Diseases, X-Linked - genetics | Ataxia - genetics | Ataxia - metabolism | Microcephaly - drug therapy | Ataxia - pathology | Ocular Motility Disorders - pathology | Tumor Suppressor Proteins - metabolism | Apolipoprotein E4 - metabolism | Endosomes - genetics | Histone Deacetylases - genetics | Ocular Motility Disorders - metabolism | Intellectual Disability - pathology | Alzheimer Disease - drug therapy | Receptors, LDL - metabolism | Mice, Knockout | Genetic Diseases, X-Linked - pathology | Epilepsy - drug therapy | Histone Deacetylase Inhibitors - pharmacology | Mice | Astrocytes - metabolism | Hydrogen-Ion Concentration | Apolipoprotein E4 - genetics | Ocular Motility Disorders - genetics | Intellectual Disability - genetics | Sodium-Hydrogen Exchangers - metabolism | Genetic Diseases, X-Linked - drug therapy | Microcephaly - pathology | Tumor Suppressor Proteins - genetics | Epilepsy - genetics | Sodium-Hydrogen Exchangers - genetics | Receptors, LDL - genetics | Microcephaly - metabolism | Histone Deacetylases - metabolism | Endosomes - pathology | Genetic Diseases, X-Linked - metabolism | Intellectual Disability - drug therapy | Ocular Motility Disorders - drug therapy | Animals | Alzheimer Disease - metabolism | Alzheimer Disease - genetics | Epilepsy - pathology | Physiological aspects | Epigenetic inheritance | Glycoproteins | Genetic aspects | Observations | Astrocytes | Protons | Brain | Membranes | Transcription | Gene regulation | Trafficking | Cognitive ability | Acidification | pH effects | Neuronal-glial interactions | Risk factors | Proteins | Apolipoprotein E | Neurodegeneration | Compartments | Down-regulation | Alzheimer's disease | Plaques | Translocation | Pathogens | Apolipoprotein E4 | Therapeutic applications | Na+/H+-exchanging ATPase | Risk analysis | Apolipoproteins | Nuclear transport | Alleles | Epigenetics | Cytopathology | Receptor density | Mutation | Alzheimers disease | Endosomes | Index Medicus | Biological Sciences | PNAS Plus | H+ exchanger | Na+
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2016, Volume 98, Issue 4, pp. 615 - 626
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 695 - 703
Journal Article