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2006, ISBN 0120885549, xvii, 687 p., [16] p. of plates
An understanding of mechanisms underlying seizure disorders depends critically on the insights provided by model systems. In particular with the development of... 
Epilepsy | Clinical & internal medicine | Animal models | Spasms
Book
The Lancet, ISSN 0140-6736, 04/2006, Volume 367, Issue 9516, pp. 1087 - 1100
Journal Article
Epileptic Disorders, ISSN 1294-9361, 12/2007, Volume 9, Issue 4, pp. 353 - 412
Background. Childhood epilepsies are a heterogeneous group of conditions that differ in diagnostic criteria and management and have dramatically different... 
Pediatric epilepsy | Expert opinion | Antiepileptic drugs | Epilepsy syndromes | Consensus | Seizures | antiepileptic drugs | COMPLEX PARTIAL SEIZURES | GUIDELINE SERIES TREATMENT | expert opinion | TEMPORAL-LOBE EPILEPSY | epilepsy syndromes | CLINICAL NEUROLOGY | consensus | VAGUS NERVE-STIMULATION | BENIGN CHILDHOOD EPILEPSY | ADD-ON THERAPY | QUALITY-STANDARDS-SUBCOMMITTEE | JUVENILE MYOCLONIC EPILEPSY | IDIOPATHIC GENERALIZED EPILEPSY | pediatric epilepsy | seizures | TECHNOLOGY-ASSESSMENT SUBCOMMITTEE | Epilepsy, Absence - therapy | Epilepsy, Benign Neonatal - epidemiology | Confidence Intervals | Epilepsy, Tonic-Clonic - therapy | Humans | Child, Preschool | Infant | Male | Epilepsy, Absence - epidemiology | Epilepsy, Complex Partial - epidemiology | Epilepsy - epidemiology | Epilepsy, Tonic-Clonic - epidemiology | Epilepsy, Complex Partial - therapy | Status Epilepticus - therapy | Adult | Female | Status Epilepticus - epidemiology | Child | Epilepsy, Benign Neonatal - therapy | Spasms, Infantile - epidemiology | Data Interpretation, Statistical | Anticonvulsants - therapeutic use | Epilepsies, Myoclonic - epidemiology | Europe - epidemiology | Spasms, Infantile - therapy | Seizures, Febrile - therapy | Adolescent | Epilepsy - drug therapy | Epilepsies, Myoclonic - therapy | Seizures, Febrile - epidemiology | Epilepsy - therapy
Journal Article
Nature Reviews Neurology, ISSN 1759-4758, 03/2012, Volume 8, Issue 3, pp. 123 - 124
Predicting response to therapy in individual patients with epilepsy is not straightforward. An exploration of long-term surgical outcomes in an epilepsy cohort... 
SEIZURE RECURRENCE | CLINICAL NEUROLOGY | METAANALYSIS | Female | Male | Epilepsies, Partial - surgery | Humans
Journal Article
NATURE REVIEWS DISEASE PRIMERS, ISSN 2056-676X, 05/2018, Volume 4
Epilepsy affects all age groups and is one of the most common and most disabling neurological disorders. The accurate diagnosis of seizures is essential as... 
LONG-TERM | BRAIN-BARRIER DYSFUNCTION | MEDICINE, GENERAL & INTERNAL | PROGRESSIVE MYOCLONUS EPILEPSY | ANTIEPILEPTIC DRUG-TREATMENT | 1ST SEIZURE | HIGH-FREQUENCY OSCILLATIONS | MIGRATING PARTIAL SEIZURES | QUALITY-OF-LIFE | SUDDEN UNEXPECTED DEATH | KETOGENIC DIET
Journal Article
Epilepsia, ISSN 0013-9580, 02/2018, Volume 59, Issue 2, pp. 389 - 402
Summary Objective Pathogenic SLC6A1 variants were recently described in patients with myoclonic atonic epilepsy (MAE) and intellectual disability (ID). We set... 
epilepsy | MAE | epilepsy genetics | SLC6A1 | MYOCLONIC-ASTATIC EPILEPSY | ATTENTION | GABA TRANSPORTERS | ILAE COMMISSION | CLASSIFICATION | TERMINOLOGY | CLINICAL NEUROLOGY | CHILDHOOD ABSENCE EPILEPSY | INTELLECTUAL DISABILITY | SEIZURES | POSITION PAPER | Epilepsy, Generalized - genetics | Epilepsies, Partial - drug therapy | Humans | Child, Preschool | Intellectual Disability - complications | Male | Electroencephalography | Neurodevelopmental Disorders - genetics | Epilepsy, Generalized - complications | Mutation, Missense | Epilepsies, Partial - physiopathology | Intellectual Disability - genetics | Young Adult | Adult | Female | Valproic Acid - therapeutic use | Language Development Disorders - physiopathology | Ataxia - genetics | Child | Epilepsies, Myoclonic - genetics | Epilepsies, Partial - complications | Ataxia - physiopathology | Genetic Association Studies | Language Development Disorders - genetics | Neurodevelopmental Disorders - complications | Anticonvulsants - therapeutic use | Epilepsies, Myoclonic - physiopathology | Treatment Outcome | Epilepsies, Myoclonic - complications | Language Development Disorders - complications | Intellectual Disability - physiopathology | GABA Plasma Membrane Transport Proteins - genetics | Phenotype | Epilepsy, Generalized - physiopathology | Epilepsy, Generalized - drug therapy | Adolescent | Ataxia - complications | Epilepsies, Myoclonic - drug therapy | Epilepsies, Partial - genetics | Mutation | Cohort Studies | Medical research | Divalproex | Epilepsy | Medicine, Experimental | Genetic aspects | Seizures (Medicine) | Valproic acid | Phenotypes | Convulsions & seizures | Sleep | Language | EEG | Cognitive ability | Speech | Ataxia | Seizures | Life Sciences | Genetics | Human genetics
Journal Article
2006, Advances in neurology, ISBN 9780781758154, Volume 97., xxvii, 595
Book
by Allen, Andrew S and Bellows, Susannah T and Berkovic, Samuel F and Bridgers, Joshua and Burgess, Rosemary and Cavalleri, Gianpiero and Chung, Seo-Kyung and Cossette, Patrick and Delanty, Norman and Dlugos, Dennis and Epstein, Michael P and Freyer, Catharine and Goldstein, David B and Heinzen, Erin L and Hildebrand, Michael S and Johnson, Michael R and Kuzniecky, Ruben and Lowenstein, Daniel H and Marson, Anthony G and Mayeux, Richard and Mebane, Caroline and Mefford, Heather C and O'Brien, Terence J and Ottman, Ruth and Petrou, Steven and Petrovski, Slavgé and Pickrell, William O and Poduri, Annapurna and Radtke, Rodney A and Rees, Mark I and Regan, Brigid M and Ren, Zhong and Scheffer, Ingrid E and Sills, Graeme J and Thomas, Rhys H and Wang, Quanli and Abou-Khalil, Bassel and Alldredge, Brian K and Amrom, Dina and Andermann, Eva and Andermann, Frederick and Bautista, Jocelyn F and Bluvstein, Judith and Boro, Alex and Cascino, Gregory D and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Fiol, Miguel and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Geller, Eric B and Glauser, Tracy and Glynn, Simon and Haas, Kevin and Haut, Sheryl R and Hayward, Jean and Helmers, Sandra L and Joshi, Sucheta and Kanner, Andres and Kirsch, Heidi E and Knowlton, Robert C and Kossoff, Eric H and Kuperman, Rachel and Motika, Paul V and Novotny, Edward J and Paolicchi, Juliann M and Parent, Jack M and Park, Kristen and Sadleir, Lynette G and Shellhaas, Renée A and Sherr, Elliott H and Shih, Jerry J and Shinnar, Shlomo and Singh, Rani K and Sirven, Joseph and Smith, Michael C and Sullivan, Joseph and Thio, Liu Lin and Venkat, Anu and Vining, Eileen P.G and Von Allmen, Gretchen K and Weisenberg, Judith L and Widdess-Walsh, Peter and Winawer, Melodie R and Epilepsy Phenome/Genome Project and Epi4K consortium and Epilepsy Phenome-Genome Proj and Epi4k Consortium
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 2, pp. 135 - 143
Summary Background Despite progress in understanding the genetics of rare epilepsies, the more common epilepsies have proven less amenable to traditional... 
Neurology | RISK | SEIZURES | CLINICAL NEUROLOGY | MUTATION | DISEASE | Epilepsy, Generalized - genetics | Exome | Genetic Variation | Genetic Predisposition to Disease | Humans | Epilepsies, Partial - genetics | Sequence Analysis, DNA | Case-Control Studies | Genetic research | Genetic aspects | Analysis | Epilepsy | Proteins | Studies | Disease | Genomes | Mutation | Family medical history | Patients
Journal Article
Epilepsia, ISSN 0013-9580, 06/2017, Volume 58, Issue 6, pp. 1005 - 1014
Summary Objective Evaluate the seizure‐reduction response and safety of brain‐responsive stimulation in adults with medically intractable partial‐onset... 
Closed‐loop | Eloquent cortex | Brain stimulation | Neuromodulation | Partial seizures | Closed-loop | SURGERY | STIMULATION | RESECTION | CLINICAL CHARACTERISTICS | SURGICAL-TREATMENT | CLINICAL NEUROLOGY | TEMPORAL-LOBE | PARIETAL LOBE EPILEPSY | PARTIAL-ONSET EPILEPSY | OUTCOMES | RESISTANT PARTIAL EPILEPSY | Epilepsy, Tonic-Clonic - therapy | Follow-Up Studies | Humans | Middle Aged | Epilepsy, Complex Partial - physiopathology | Male | Electroencephalography | Cerebral Cortex - physiopathology | Epilepsies, Partial - physiopathology | Feasibility Studies | Young Adult | Epilepsy, Complex Partial - therapy | Neocortex - physiopathology | Epilepsy, Partial, Motor - therapy | Adult | Female | Epilepsies, Partial - therapy | Electric Stimulation Therapy - instrumentation | Epilepsy, Partial, Motor - physiopathology | Electrodes, Implanted | Deep Brain Stimulation - instrumentation | Deep Brain Stimulation - methods | Electric Stimulation Therapy - methods | Adolescent | Brain Mapping | Drug Resistant Epilepsy - therapy | Epilepsy, Tonic-Clonic - physiopathology | Drug Resistant Epilepsy - physiopathology | Complications and side effects | Brain | Care and treatment | Seizures (Medicine) | Epilepsy | Neuroimaging | Nuclear magnetic resonance--NMR | Cortex | Clinical trials | Chronic infection | Hemorrhage | Magnetic resonance imaging | Cortex (parietal) | Surgery | Cortex (frontal) | Vagus nerve | Cortex (temporal) | Seizures
Journal Article