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European Journal of Paediatric Neurology, ISSN 1090-3798, 2012, Volume 16, Issue 1, pp. S5 - S8
Journal Article
Brain : a journal of neurology, 08/2019, Volume 142, Issue 8, p. 2173
Journal Article
Epilepsy Currents, ISSN 1535-7597, 07/2018, Volume 18, Issue 4, pp. 238 - 239
Journal Article
Epilepsy Currents, ISSN 1535-7597, 10/2019, p. 153575971987941
[Box: see text] 
Journal Article
The Lancet Neurology, ISSN 1474-4422, 01/2018, Volume 17, Issue 1, pp. 7 - 8
Journal Article
Epilepsia, ISSN 0013-9580, 06/2011, Volume 52, Issue 6, pp. 1058 - 1062
Concepts and terminology for classifying seizures and epilepsies have, until recently, rested on ideas developed nearly a century ago. In order for clinical... 
Etiology | Seizure semiology | Classification | GLUT1 | EPILEPTIC SEIZURES | PROPOSAL | CORTICAL DEVELOPMENT | ONSET | CLINICAL NEUROLOGY | Terminology as Topic | Epilepsy - classification | History, 21st Century | Humans | Epilepsy - diagnosis | Epilepsy | Seizures (Medicine) | Frustration | Seizures
Journal Article
Neuropediatrics, ISSN 0174-304X, 04/2014, Volume 45, Issue 2, pp. 070 - 074
Abstract Objectives  Epilepsy genetics has undergone a revolution in the past 19 years since the discovery of the first gene for epilepsy. The story of our... 
Review Article | epilepsy | epileptic encephalopathies | genetics | DEPDC5 | epilepsy syndromes | CHROMOSOME 22Q12 | FRONTAL-LOBE EPILEPSY | VARIABLE FOCI | DISORDERS | FAMILIAL PARTIAL EPILEPSY | PHENOTYPIC SPECTRUM | CLINICAL NEUROLOGY | 15Q13.3 MICRODELETIONS | IDIOPATHIC GENERALIZED EPILEPSY | DE-NOVO MUTATIONS | PEDIATRICS | LINKAGE
Journal Article
Epilepsia, ISSN 0013-9580, 01/2011, Volume 52, Issue 1, pp. 192 - 193
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2015, Volume 14, Issue 12, pp. 1147 - 1148
  Genetic insights are blurring the boundaries of a classification based on the developmental processes of cell proliferation, neuronal migration, and... 
Neurology | CLINICAL NEUROLOGY | MALFORMATIONS | MUTATIONS | Phosphatidylinositol 3-Kinases - genetics | Malformations of Cortical Development - genetics | Mutation | Humans | Abnormalities, Multiple - genetics | Intellectual Disability - genetics | Families & family life | Cell growth | Kinases | Deoxyribonucleic acid--DNA
Journal Article
The Lancet Neurology, ISSN 1474-4422, 04/2019, Volume 18, Issue 4, pp. 335 - 336
[...]Dravet syndrome is usually caused by mutations in SCN1A, a gene that codifies for a neuronal sodium channel subunit; the function of the protein is... 
Climate change | Convulsions & seizures | Meetings | Temperature effects | Epilepsy | Carbon dioxide | Sodium channels (voltage-gated) | Mutation | Gene expression | Antiepileptic agents | Seizures | Emissions
Journal Article
Journal Article
Epilepsia, ISSN 0013-9580, 04/2014, Volume 55, Issue 4, pp. 475 - 482
Journal Article