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Lancet neurology, ISSN 1474-4422, 2016, Volume 15, Issue 3, pp. 304 - 316
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Brain Diseases - therapy | Humans | Brain Diseases - genetics | Child, Preschool | Epilepsy - genetics | Infant | Brain Diseases - etiology | Epilepsy - physiopathology | Child | Brain Diseases - physiopathology | Epilepsy - therapy | Epilepsy - complications | Proteins | Genetic research | Neurosciences | Seizures (Medicine) | Children's hospitals | Epilepsy | Autism | Age | Index Medicus
Journal Article
Lancet neurology, ISSN 1474-4422, 2014, Volume 13, Issue 11, pp. 1114 - 1126
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Epilepsy - surgery | Adult | Treatment Outcome | Neurosurgical Procedures - methods | Neurosurgical Procedures - trends | Electroencephalography - trends | Epilepsy - physiopathology | Child | Electroencephalography - methods | Epilepsy - diagnosis | Seizures (Medicine) | Drug resistance | Surgery | Epilepsy | Neurophysiology | Studies | Quality of life | Index Medicus
Journal Article
The New England journal of medicine, ISSN 0028-4793, 10/2017, Volume 377, Issue 17, pp. 1648 - 1656
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Age Factors | Europe | Humans | Brain Neoplasms - pathology | Epilepsy - surgery | Male | Hippocampus - pathology | Brain Neoplasms - complications | Epilepsy - etiology | Malformations of Cortical Development - complications | Databases as Topic | Age of Onset | Brain - pathology | Adult | Female | Malformations of Cortical Development - pathology | Temporal Lobe - pathology | Child | Epilepsy - pathology | Brain | Usage | Care and treatment | Surgery | Epilepsy | Analysis | Research | Histology, Pathological | Temporal lobe | Pediatrics | Dysplasia | Nuclear magnetic resonance--NMR | Neuropathology | Cortex | Neurosurgery | Drug resistance | Patients | Sclerosis | Studies | Neurology | Histopathology | Children | Hippocampus | Seizures | Tumors | Index Medicus | Abridged Index Medicus
Journal Article
Epilepsia (Copenhagen), ISSN 0013-9580, 2011, Volume 52, Issue 1, pp. 158 - 174
Cortical dysplasia | Hippocampal sclerosis | Neuropathology | Epilepsy | Seizures | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Malformations of the nervous system | Medical sciences | Nervous system (semeiology, syndromes) | Malformations of Cortical Development - diagnosis | Global Health | Humans | Cerebral Cortex - pathology | Advisory Committees - standards | Malformations of Cortical Development - pathology | Societies, Medical - standards | Cerebral Cortex - abnormalities | Malformations of Cortical Development - classification | Medical colleges | Encephalitis | Task forces | Dysplasia | Neurosciences | Surgical clinics | Neurons | Children's hospitals | Diagnostic imaging | Adults | Seizures (Medicine) | Diagnosis | Children | Health aspects | Methods | Histochemistry | Tumors | Brain | Classification | Index Medicus | Neuroimaging | Cortex | Classification systems | Data processing | Sclerosis | Ischemia | Hippocampus | Injuries | World Health | Cerebral Cortex | Societies, Medical | Malformations of Cortical Development | Advisory Committees
Journal Article
2013, ISBN 9780071496216, xvii, 507
Book
Nature nanotechnology, ISSN 1748-3387, 2014, Volume 9, Issue 1, pp. 44 - 47
Science & Technology - Other Topics | Materials Science | Nanoscience & Nanotechnology | Technology | Materials Science, Multidisciplinary | Science & Technology | Nanostructures - chemistry | Protein Binding | Microtubules - chemistry | DNA - chemistry | Dyneins - chemistry | Kinesin - chemistry | Index Medicus | Proteins | Networks | Tasks | Deoxyribonucleic acid | Motors | Transport | Arrays | Assembly
Journal Article
Epilepsia (Copenhagen), ISSN 0013-9580, 09/2012, Volume 53, Issue 4, pp. 3 - 8
Febrile seizures | Temporal lobe epilepsy | Fever‐induced epileptic encephalopathy | Dravet syndrome | Fever-induced epileptic encephalopathy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Pharmacology. Drug treatments | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Biological and medical sciences | Anticonvulsants. Antiepileptics. Antiparkinson agents | Medical sciences | Neuropharmacology | Nervous system (semeiology, syndromes) | Meningitis - complications | Seizures, Febrile - physiopathology | Fever - complications | Humans | Risk Factors | Epilepsy, Temporal Lobe - physiopathology | Epilepsy - physiopathology | Seizures, Febrile - etiology | Child | Epilepsy - etiology | Fever - physiopathology | Children's hospitals | Epilepsy | Seizures (Medicine) | Convulsions & seizures | Fever | Children & youth | Index Medicus
Journal Article
Nature (London), ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | Index Medicus | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article