| scholarly article | Q13442814 |
| P2093 | author name string | J Engel | |
| P2860 | cites work | Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy | Q28243859 |
| Clinical and electroencephalographical classification of epileptic seizures | Q28251225 | ||
| Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy | Q28273764 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | diagnosis | Q16644043 |
| P304 | page(s) | 796-803 | |
| P577 | publication date | 2001-06-01 | |
| P1433 | published in | Epilepsia | Q5382969 |
| P1476 | title | A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology | |
| P478 | volume | 42 |
| Q37969852 | "Electro-clinical syndromes" with onset in paediatric age: the highlights of the clinical-EEG, genetic and therapeutic advances |
| Q37883054 | "Epileptic encephalopathy" of infancy and childhood: electro-clinical pictures and recent understandings |
| Q43291757 | A 12-month longitudinal study of calcium metabolism and bone turnover during valproate monotherapy. |
| Q90599497 | A Model of Chronic Temporal Lobe Epilepsy Presenting Constantly Rhythmic and Robust Spontaneous Seizures, Co-morbidities and Hippocampal Neuropathology |
| Q38246632 | A Molecular Approach to Epilepsy Management: from Current Therapeutic Methods to Preconditioning Efforts |
| Q48503182 | A clinical and magnetoencephalography study of MRI-negative startle epilepsy. |
| Q38580125 | A definition and classification of status epilepticus--Report of the ILAE Task Force on Classification of Status Epilepticus. |
| Q89185651 | A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23 |
| Q48297410 | A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome |
| Q83437018 | A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3. |
| Q42087667 | A neuropsychological assessment, using computerized battery tests (CANTAB), in children with benign rolandic epilepsy before AED therapy. |
| Q48200417 | A new case of idiopathic hemiplegia hemiconvulsion syndrome |
| Q42136947 | A new generation of anticonvulsants for the treatment of epilepsy in children |
| Q34464870 | A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes. |
| Q43529572 | A population-based study of newly diagnosed epilepsy in infants. |
| Q51620790 | A profile of adolescent-onset epilepsy. |
| Q35929989 | A proposal for case definitions and outcome measures in studies of infantile spasms and West syndrome: consensus statement of the West Delphi group |
| Q47904248 | A prospective study of dexamethasone therapy in refractory epileptic encephalopathy with continuous spike-and-wave during sleep |
| Q44602436 | A psychosocial view of anxiety and depression in epilepsy |
| Q88266802 | A rare finding in epilepsy with myoclonic absences: focal seizure |
| Q92451478 | A reflection on the role of genetics in the concept of "epileptic encephalopathy", as emerged from the most recent ILEA classification of epilepsy |
| Q46839326 | A resting-state functional connectivity study in patients at high risk for sudden unexpected death in epilepsy |
| Q33160174 | A retrospective population-based study on seizures related to childhood vaccination |
| Q91841215 | AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders |
| Q38613828 | Aberrant Thalamocortical Connectivity in Juvenile Myoclonic Epilepsy |
| Q97641154 | Aberrant dorsal attention network homogeneity in patients with right temporal lobe epilepsy |
| Q37205702 | Aberrant long-range functional connectivity density in generalized tonic-clonic seizures |
| Q60934594 | Abnormalities of diffusional kurtosis imaging and regional homogeneity in idiopathic generalized epilepsy with generalized tonic-clonic seizures |
| Q51817589 | Absence seizures in the first 3 years of life: an electroclinical study of 46 cases. |
| Q35726686 | Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome |
| Q42640395 | Absence status epilepsy: delineation of a distinct idiopathic generalized epilepsy syndrome |
| Q50711374 | Adjunctive zonisamide therapy in the long-term treatment of children with partial epilepsy: results of an open-label extension study of a phase III, randomized, double-blind, placebo-controlled trial. |
| Q28304952 | Adult epilepsy |
| Q53697856 | Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population-based study. |
| Q90838035 | Affect-induced reflex seizures (AIRS): A case series based on a systematic literature review |
| Q50868832 | Alterations in white matter microstructures and cognitive dysfunctions in benign childhood epilepsy with centrotemporal spikes. |
| Q37235891 | Altered Effective Connectivity among Core Neurocognitive Networks in Idiopathic Generalized Epilepsy: An fMRI Evidence |
| Q42369989 | Altered Local Spatiotemporal Consistency of Resting-State BOLD Signals in Patients with Generalized Tonic-Clonic Seizures. |
| Q36448488 | Altered Local Spontaneous Brain Activity in Juvenile Myoclonic Epilepsy: A Preliminary Resting-State fMRI Study |
| Q57064288 | Altered Proteins in the Hippocampus of Patients with Mesial Temporal Lobe Epilepsy |
| Q48101621 | Altered Structural and Functional Feature of Striato-Cortical Circuit in Benign Epilepsy with Centrotemporal Spikes |
| Q37205604 | Altered functional and effective connectivity in anticorrelated intrinsic networks in children with benign childhood epilepsy with centrotemporal spikes. |
| Q40984291 | Altered functional connectivity among default, attention, and control networks in idiopathic generalized epilepsy |
| Q33819985 | Altered functional connectivity in default mode network in absence epilepsy: a resting-state fMRI study. |
| Q30552416 | Altered functional connectivity within and between brain modules in absence epilepsy: a resting-state functional magnetic resonance imaging study |
| Q48859663 | Altered functional-structural coupling of large-scale brain networks in idiopathic generalized epilepsy |
| Q37404605 | Altered local spontaneous activity in frontal lobe epilepsy: a resting-state functional magnetic resonance imaging study |
| Q44640011 | Altered resting-state connectivity during interictal generalized spike-wave discharges in drug-naïve childhood absence epilepsy |
| Q59147102 | An IoT Platform for Epilepsy Monitoring and Supervising |
| Q47694824 | Analysis of clinical characteristics and risk factors for mortality in human status epilepticus |
| Q98944341 | Analysis of the aetiology of epilepsy in 3,216 adult patients attending a tertiary referral center enabled by an electronic patient record |
| Q47663609 | Anatomical and physiological basis of continuous spike-wave of sleep syndrome after early thalamic lesions |
| Q90251211 | Antagonizing Increased miR-135a Levels at the Chronic Stage of Experimental TLE Reduces Spontaneous Recurrent Seizures |
| Q24202269 | Antiepileptic drugs for the primary and secondary prevention of seizures after subarachnoid haemorrhage |
| Q24235826 | Antiepileptic drugs for the primary and secondary prevention of seizures after subarachnoid haemorrhage |
| Q44767098 | Applicability of the new ILAE classification for epilepsies (2010) in persons with epilepsy at a tertiary care center in India |
| Q48516483 | Assessment of mothers' knowledge and perceptions of electroencephalography and determination of the short-term effect of an informational leaflet |
| Q35728997 | Association analysis of polymorphisms of the CRHR1 gene with infantile spasms |
| Q41445901 | Association between PK/PD-involved gene polymorphisms and carbamazepine-individualized therapy. |
| Q80038760 | Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits |
| Q34122468 | Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity. |
| Q41673432 | Attention Contributes to Arithmetic Deficits in New-Onset Childhood Absence Epilepsy |
| Q42619127 | Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions. |
| Q52092732 | Atypical handedness in mesial temporal lobe epilepsy. |
| Q27324195 | Audiogenic reflex seizures in cats |
| Q58617784 | Audiogenic reflex seizures in cats |
| Q36720971 | Autism and epilepsy: what has regression got to do with it? |
| Q45730334 | Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies. |
| Q48389904 | Autonomic seizures and autonomic status epilepticus in early onset benign childhood occipital epilepsy (Panayiotopoulos syndrome). |
| Q33151391 | Autonomic seizures and autonomic status epilepticus peculiar to childhood: diagnosis and management |
| Q36794856 | Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: a consensus view |
| Q50280469 | Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype |
| Q38488233 | BCL2A1 is a potential biomarker for postoperative seizure control in patients with low-grade gliomas |
| Q64104606 | BOLD-fMRI activity informed by network variation of scalp EEG in juvenile myoclonic epilepsy |
| Q42176475 | Beating the Odds: Intact Neuropsychological Functioning despite TLE |
| Q35630222 | Behavioral aspects of pediatric epilepsy syndromes |
| Q44534343 | Behavioral problems, cognitive difficulties and quality of life in children with epilepsy: an analysis of parental concerns |
| Q41441581 | Benign childhood epilepsy with Centro-Temporal spikes (BCECTSs), electrical status epilepticus in sleep (ESES), and academic decline--how aggressive should we be? |
| Q51755047 | Benign childhood epilepsy with centro-temporal spikes: evolutive clinical, cognitive and EEG aspects |
| Q38040440 | Benign childhood focal epilepsies |
| Q53663086 | Benign familial infantile seizures: further delineation of the syndrome. |
| Q48571749 | Benign focal seizures of adolescence: a prospective study |
| Q48479752 | Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases |
| Q37873696 | Benign partial seizures of adolescence |
| Q44443528 | Bilateral akinetic seizures: a clinical and electroencephalographic description. |
| Q37946402 | Biomarkers in epilepsy: introduction |
| Q46208501 | Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy |
| Q33998418 | Brain development in children with new onset epilepsy: a prospective controlled cohort investigation |
| Q37504714 | Brain mechanisms of altered conscious states during epileptic seizures |
| Q28481566 | Brain-derived neurotrophic factor ameliorates brain stem cardiovascular dysregulation during experimental temporal lobe status epilepticus |
| Q38195636 | Brivaracetam for the treatment of epilepsy in adults. |
| Q47714716 | CNTNAP4 Impacts Epilepsy Through GABAA Receptors Regulation: Evidence From Temporal Lobe Epilepsy Patients and Mouse Models |
| Q36254491 | Canine epilepsy: what can we learn from human seizure disorders? |
| Q30511881 | Carbamazepine inhibits angiotensin I-converting enzyme, linking it to the pathogenesis of temporal lobe epilepsy. |
| Q35172342 | Cellular biology of epileptogenesis |
| Q48415900 | Cerebellar hypoplasia, continuous spike-waves during sleep, and neuropsychological and behavioral disorders |
| Q36341748 | Challenges and opportunities in the application of pharmacogenetics to antiepileptic drug therapy |
| Q55396526 | Changes in Dynamics Within and Between Resting-State Subnetworks in Juvenile Myoclonic Epilepsy Occur at Multiple Frequency Bands. |
| Q37939980 | Changing perspectives on Landau-Kleffner syndrome |
| Q37368370 | Child Neurology: Dravet syndrome: when to suspect the diagnosis |
| Q48460165 | Childhood epilepsy with occipital paroxysms: difficulties in distinct segregation into either the early-onset or late-onset epilepsy subtypes |
| Q37023438 | Childhood epilepsy with occipital paroxysms: variations on the theme |
| Q35132992 | Childhood epilepsy: what is the evidence for what we think and what we do? |
| Q48456347 | Childhood occipital epilepsy of Gastaut: a study of 33 patients |
| Q41947085 | Children with epilepsy: why can't they pay attention? |
| Q34590975 | Chronic disorders with episodic manifestations: focus on epilepsy and migraine |
| Q28396131 | Chronopharmacology of anti-convulsive therapy |
| Q80035094 | Chvostek's sign and hypocalcaemia in children with seizures |
| Q35617456 | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
| Q50646208 | Classification Preictal and Interictal Stages via Integrating Interchannel and Time-Domain Analysis of EEG Features. |
| Q35204002 | Classification of seizures and epilepsy |
| Q53061379 | Classifying normal and abnormal status based on video recordings of epileptic patients. |
| Q80059162 | Clinical and electroencephalographic characteristics of children with febrile seizures plus |
| Q48914486 | Clinical and molecular genetic factors affecting postoperative seizure control of 183 Chinese adult patients with low-grade gliomas |
| Q38113673 | Clinical aspects of juvenile myoclonic epilepsy |
| Q34201435 | Clinical characteristics and outcome of children with electrical status epilepticus during slow wave sleep |
| Q92551433 | Clinical features and treatment outcomes of Juvenile myoclonic epilepsy patients |
| Q38213837 | Clinical management of epileptic encephalopathies of childhood and infancy |
| Q73059068 | Clinical presentations of naturally occurring canine seizures: similarities to human seizures |
| Q34195259 | Clinical significance of serological biomarkers and neuropsychological performances in patients with temporal lobe epilepsy |
| Q37106005 | Clinical trial design in status epilepticus: problems and solutions |
| Q38537384 | Clonazepam in the treatment of status epilepticus. |
| Q46326531 | Cognitive Function and Heat Shock Protein 70 in Children With Temporal Lobe Epilepsy |
| Q36653829 | Cognitive and behavioral outcomes of epileptic syndromes: implications for education and clinical practice |
| Q88166925 | Cognitive and clinical variables associated with interictal dysphoric disorder in patients with epilepsy |
| Q36215529 | Cognitive consequences of early versus late antiepileptic drug withdrawal after pediatric epilepsy surgery, the TimeToStop (TTS) trial: study protocol for a randomized controlled trial |
| Q37861261 | Cognitive development in children with Dravet syndrome |
| Q30580712 | Cognitive development in children with new onset epilepsy |
| Q48935194 | Cognitive functioning in bilateral perisylvian polymicrogyria (BPP): clinical and radiological correlations. |
| Q48339561 | Cognitive phenotypes in temporal lobe epilepsy |
| Q28546107 | Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsies |
| Q81723238 | Comparison of classifications of seizures: a preliminary study with 28 participants and 48 seizures |
| Q39782946 | Complex discharge-affecting networks in juvenile myoclonic epilepsy: A simultaneous EEG-fMRI study |
| Q90296848 | Comprehensive analysis of presurgical factors predicting psychiatric disorders in patients with refractory temporal lobe epilepsy and mesial temporal sclerosis underwent cortico-amygdalohippocampectomy |
| Q37204997 | Computer modelling of epilepsy |
| Q26864642 | Conceptual distinctions between reflex and nonreflex precipitated seizures in the epilepsies: a systematic review of definitions employed in the research literature |
| Q36729233 | Concise review: prospects of stem cell therapy for temporal lobe epilepsy. |
| Q30620276 | Consciousness in Focal Seizures: Either You're In or You're Out |
| Q36208326 | Consciousness, epilepsy, and emotional qualia. |
| Q33167451 | Convulsive Syncope Induced by Ventricular Arrhythmia Masquerading as Epileptic Seizures: Case Report and Literature Review |
| Q55263907 | Corilagin Reduces the Frequency of Seizures and Improves Cognitive Function in a Rat Model of Chronic Epilepsy. |
| Q57126031 | Correlation between clinical and cognitive aspects and nutritional indicators of elderly patients with new-onset epilepsy |
| Q35160750 | Correlation between human seizure-related gene 6 variants and idiopathic generalized epilepsy in a Southern Chinese Han population |
| Q87859995 | Correlation of the UGT1A4 gene polymorphism with serum concentration and therapeutic efficacy of lamotrigine in Han Chinese of Northern China |
| Q30490007 | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
| Q36470061 | Cryptogenic localization-related epilepsy with childhood onset: The problem of definition and prognosis |
| Q38946719 | Current Treatment Options for Early-Onset Pediatric Epileptic Encephalopathies |
| Q34599744 | Current dipole orientation and distribution of epileptiform activity correlates with cortical thinning in left mesiotemporal epilepsy |
| Q47688880 | Cyclic alternating pattern and interictal epileptiform discharges during morning sleep after sleep deprivation in temporal lobe epilepsy. |
| Q40558873 | De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy |
| Q35275423 | Death within 8 years after childhood convulsive status epilepticus: a population-based study |
| Q38656474 | Deep belief networks for electroencephalography: A review of recent contributions and future outlooks |
| Q34690709 | Deficits in oculomotor performance in pediatric epilepsy |
| Q48290168 | Definition and natural history of Lennox-Gastaut syndrome |
| Q34754651 | Deformation-based morphometry of prospective neurodevelopmental changes in new onset paediatric epilepsy |
| Q48183901 | Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome. |
| Q37586627 | Detection of epileptic seizure event and onset using EEG |
| Q48096992 | Determinants of quality of life in people with epilepsy in Serbia |
| Q46716550 | Developing the Pediatric Refractory Epilepsy Questionnaire: a pilot study |
| Q47701343 | Development of diagnostic reference frames for seizures. Part 2: are seizure descriptions discriminative? |
| Q38174060 | Diagnostic approach of epilepsy in childhood and adolescence |
| Q34579431 | Diagnostic difficulty in infants and children |
| Q33546410 | Diagnostic methods for extra-temporal neocortical focal epilepsies: present and future |
| Q90556054 | Different patterns of white matter changes after successful surgery of mesial temporal lobe epilepsy |
| Q48943968 | Differential neuroprotection by A(1) receptor activation and A(2A) receptor inhibition following pilocarpine-induced status epilepticus. |
| Q57817983 | Disrupted Coupling Between the Spontaneous Fluctuation and Functional Connectivity in Idiopathic Generalized Epilepsy |
| Q48599843 | Disrupted structural and functional rich club organization of the brain connectome in patients with generalized tonic-clonic seizure |
| Q52618386 | Distinct white matter abnormalities in different idiopathic generalized epilepsy syndromes. |
| Q46475653 | Distribution and predictive factors of seizure types in 104 cases |
| Q81285558 | Do video games evoke specific types of epileptic seizures? |
| Q37783464 | Documentation of autonomic seizures and autonomic status epilepticus with ictal EEG in Panayiotopoulos syndrome. |
| Q51900383 | Does greater low frequency EEG activity in normal immaturity and in children with epilepsy arise in the same neuronal network? |
| Q35275382 | Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology |
| Q44707887 | Dravet syndrome, SUDEP, and omega-3 fatty acids: Lessons from the past, learning of the present, and perspectives for the future |
| Q38212437 | Dravet syndrome--from epileptic encephalopathy to channelopathy |
| Q33159969 | Dreaming experience as a useful diagnostic clue for syncopal episodes |
| Q92135825 | Dynamic Neuromagnetic Network Changes of Seizure Termination in Absence Epilepsy: A Magnetoencephalography Study |
| Q48482376 | Dynamic functional network connectivity in idiopathic generalized epilepsy with generalized tonic-clonic seizure |
| Q92777236 | Dysfunctional white-matter networks in medicated and unmedicated benign epilepsy with centrotemporal spikes |
| Q48549119 | Early thalamic injury associated with epilepsy and continuous spike-wave during slow sleep |
| Q26773828 | Early-onset epileptic encephalopathies and the diagnostic approach to underlying causes |
| Q37847228 | Early-onset pure absence epilepsy: a distinct epileptic syndrome |
| Q39599780 | Eating Epilepsy in Oman: A case series and report on the efficacy of temporal lobectomy |
| Q47618557 | Effects of spontaneous recurrent seizures on cognitive function via modulation of SNAREs expression |
| Q43271749 | Efficacy and safety of levetiracetam as an add-on therapy in children aged less than 4 years with refractory epilepsy |
| Q37869621 | Efficacy and safety of methylphenidate in treating ADHD symptoms in children and adolescents with uncontrolled seizures: a Brazilian sample study and literature review |
| Q44792559 | Efficacy and tolerability of levetiracetam in patients with therapy-resistant epilepsy and learning disabilities |
| Q46539314 | Efficacy and tolerability of pregabalin in patients with difficult-to-treat epilepsy and intellectual disability |
| Q59222837 | Elderly People and Epilepsy: Cognitive Function |
| Q47735504 | Electroclinical findings of minor motor events during sleep in temporal lobe epilepsy |
| Q48825413 | Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patients |
| Q53887628 | Electroencephalography abnormalities in generalized epilepsy and their predictors: A multicenter experience. |
| Q33958421 | Emerging role of the KCNT1 Slack channel in intellectual disability |
| Q26749102 | Emerging surgical therapies in the treatment of pediatric epilepsy |
| Q50777077 | Emotional stress-induced seizures: another reflex epilepsy? |
| Q38283089 | Epidemiology and clinical manifestations of juvenile myoclonic epilepsy (JME) in Iran |
| Q51830067 | Epilepsia partialis continua in children with fulminant subacute sclerosing panencephalitis |
| Q43711186 | Epilepsy among children and adolescents with autism spectrum disorders: a population-based study. |
| Q34260757 | Epilepsy and epileptic syndrome. |
| Q29039028 | Epilepsy and mental retardation limited to females: an under-recognized disorder |
| Q38247539 | Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritance. |
| Q48212703 | Epilepsy and quality of life: socio-demographic and clinical aspects, and psychiatric co-morbidity |
| Q36473943 | Epilepsy as part of systemic lupus erythematosus and systemic antiphospholipid syndrome (Hughes syndrome). |
| Q44420556 | Epilepsy in Colombia: epidemiologic profile and classification of epileptic seizures and syndromes |
| Q26783630 | Epilepsy in India I: Epidemiology and public health |
| Q54654702 | Epilepsy in Rett syndrome: clinical and genetic features. |
| Q48773947 | Epilepsy in cerebral glioma: timing of appearance and histological correlations. |
| Q37560645 | Epilepsy in childhood and adolescence |
| Q34493734 | Epilepsy in children |
| Q48782979 | Epilepsy in horses: aetiological classification and predictive factors |
| Q48555819 | Epilepsy in shunted posthemorrhagic infantile hydrocephalus owing to pre- or perinatal intra- or periventricular hemorrhage |
| Q48573460 | Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities |
| Q37301523 | Epilepsy in women: special considerations for adolescents |
| Q79254576 | Epilepsy with myoclonic absences |
| Q48339328 | Epilepsy with onset at over 50 years of age: clinical and electroencephalographic characteristics |
| Q35544125 | Epilepsy, antiepileptic drugs (AEDs) and cognition. |
| Q47712095 | Epilepsy, stigma, and family |
| Q57905566 | Epilepsy: A classification for all seasons? |
| Q36377765 | Epilepsy: a review of selected clinical syndromes and advances in basic science |
| Q50569040 | Epileptic activity is a surrogate for an underlying etiology and stopping the activity has a limited impact on developmental outcome. |
| Q83617154 | Epileptic aura and qualitative alterations of consciousness in focal seizures: a neuropsychiatric approach |
| Q38040452 | Epileptic encephalopathies (including severe epilepsy syndromes). |
| Q36302381 | Epileptic encephalopathies in adults and childhood |
| Q36429549 | Epileptic encephalopathies: an overview |
| Q27027982 | Epileptic encephalopathies: new genes and new pathways |
| Q38700237 | Epileptic encephalopathy: Use and misuse of a clinically and conceptually important concept |
| Q53311734 | Epileptic seizures in Behçet disease. |
| Q80375284 | Epileptiform EEG discharges in benign childhood epilepsy with centrotemporal spikes: reactivity and transitory cognitive impairment |
| Q48359470 | Evaluation of deep gray matter volume, cortical thickness and white matter integrity in patients with typical absence epilepsy: a study using voxelwise-based techniques. |
| Q36319435 | Evidence-based treatment of idiopathic generalized epilepsies with older antiepileptic drugs |
| Q97638645 | Ex vivo mesoscopic diffusion MRI correlates with seizure frequency in patients with uncontrolled mesial temporal lobe epilepsy |
| Q53426677 | Executive Dysfunction and Depression in Pediatric Temporal Lobe Epilepsy: The Contribution of Hippocampal Sclerosis and Psychosocial Factors. |
| Q104571098 | Executive function and depressed mood are independently disruptive to health-related quality of life in pediatric temporal lobe epilepsy |
| Q87014188 | Eyelid myoclonia seizures in adults: An alternate look at the syndrome paradox |
| Q92323973 | Facial emotion perception and social competence in children (8 to 16 years old) with genetic generalized epilepsy and temporal lobe epilepsy |
| Q48523738 | Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28. |
| Q40154151 | Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families |
| Q38086608 | Fasudil and its analogs: a new powerful weapon in the long war against central nervous system disorders? |
| Q35280065 | Febrile seizures: an update |
| Q35811060 | Fever, genes, and epilepsy |
| Q48169179 | Findings on low-field cranial MR images in epileptic dogs that lack interictal neurological deficits |
| Q53134917 | Focal epilepsies in adult patients attending two epilepsy centers: classification of drug-resistance, assessment of risk factors, and usefulness of "new" antiepileptic drugs. |
| Q48498527 | Focal features in patients with idiopathic generalized epilepsy |
| Q46713944 | Focal interictal epileptiform discharges in idiopathic generalized epilepsy. |
| Q45074542 | Focal seizures and consciousness |
| Q47288120 | Forty Years of Sodium Channels: Structure, Function, Pharmacology, and Epilepsy |
| Q33715193 | Functional Network Connectivity Patterns between Idiopathic Generalized Epilepsy with Myoclonic and Absence Seizures |
| Q49032692 | Functional neuroimaging in startle epilepsy: involvement of a mesial frontoparietal network |
| Q50077087 | Gene mutations in unexplained infantile epileptic encephalopathy: an analysis of 47 cases |
| Q47712380 | Generalized Models for the Classification of Abnormal Movements in Daily Life and its Applicability to Epilepsy Convulsion Recognition |
| Q35635812 | Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations |
| Q47722649 | Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families. |
| Q36344259 | Genetic focal epilepsies: state of the art and paths to the future |
| Q37470667 | Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. |
| Q35232595 | Genome-wide circulating microRNA expression profiling indicates biomarkers for epilepsy |
| Q59698070 | Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation |
| Q36192088 | Genome-wide microRNA profiling of human temporal lobe epilepsy identifies modulators of the immune response |
| Q34296136 | Glutamate transporter EAAT2: a new target for the treatment of neurodegenerative diseases |
| Q36055882 | Gray and White Matter Volumes and Cognitive Dysfunction in Drug-Naïve Newly Diagnosed Pediatric Epilepsy |
| Q34066546 | Growing up with epilepsy: a two-year investigation of cognitive development in children with new onset epilepsy |
| Q34495759 | Guidelines for epilepsy management in India classification of seizures and epilepsy syndromes |
| Q60460170 | Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy |
| Q36332667 | Headache, epilepsy and photosensitivity: how are they connected? |
| Q40059005 | Heart rate variability in untreated newly diagnosed temporal lobe epilepsy: Evidence for ictal sympathetic dysregulation |
| Q46776030 | Heterogeneity of anatomic regions by MR volumetry in juvenile myoclonic epilepsy |
| Q31034651 | Hot water epilepsy with cerebral lesion: a report of five cases with cranial MRI findings |
| Q34024199 | Hot water epilepsy with pachygyria. |
| Q30878215 | Hot water epilepsy: Phenotype and single photon emission computed tomography observations |
| Q37046642 | Hot-water epilepsy: From bench to bedside |
| Q57982315 | ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies |
| Q46206411 | ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology |
| Q33768791 | Ictal blinking, an under-recognized phenomenon: our experience and literature review |
| Q34839837 | Ictal headache and visual sensitivity |
| Q53567954 | Identification and treatment of acute repetitive seizures in children and adults. |
| Q56461699 | Idiopathic Generalized Epilepsies Recognized by the International League Against Epilepsy |
| Q33517078 | Idiopathic childhood occipital epilepsy of Gastaut: a review and differentiation from migraine and other epilepsies |
| Q40447546 | Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities. |
| Q36319403 | Idiopathic generalized epilepsies imitating focal epilepsies |
| Q36307856 | Idiopathic generalized epilepsies: clinical and electroencephalogram diagnosis and treatment |
| Q51771120 | Idiopathic generalized epilepsy with generalized tonic-clonic seizures (IGE-GTC): a population-based cohort with >20 year follow up for medical and social outcome. |
| Q84394106 | Idiopathic mesial temporal lobe epilepsy: don't sow the tares with the wheat! |
| Q48604485 | Idiopathic occipital and absence epilepsies appearing in the same children |
| Q44484036 | Imaging foci of epileptic discharges from simultaneous EEG and fMRI using the canonical HRF |
| Q38165168 | Immune mechanisms in epileptogenesis |
| Q40205007 | Impact of idiopathic epilepsy on mothers and fathers: strain, burden of care, worries and perception of vulnerability |
| Q44492062 | In search of the Rosetta Stone for ESES. |
| Q40200110 | In vivo MRI signatures of hippocampal subfield pathology in intractable epilepsy |
| Q51169628 | Incidence of childhood and adolescence epilepsy: a community-based prospective study in the province of Ferrara and in Copparo, Italy, 1996-2005. |
| Q46116471 | Incidence of epilepsy in Ferrara, Italy |
| Q50769429 | Incidence of unprovoked seizures and epilepsy in Iceland and assessment of the epilepsy syndrome classification: a prospective study. |
| Q36610296 | Increased glial glutamate transporter EAAT2 expression reduces epileptogenic processes following pilocarpine-induced status epilepticus |
| Q26778081 | Infantile Apparent Life-Threatening Events, an Educational Review |
| Q34132903 | Infantile seizures and epilepsy syndromes |
| Q83324418 | Infantile seizures and other epileptic phenotypes in a Chinese family with a missense mutation of KCNQ2 |
| Q37155958 | Infantile seizures: infants are not just little children. |
| Q43779452 | Informatics-a computational approach to the complexity of the epilepsies |
| Q35226085 | Inherited neuronal ion channelopathies: new windows on complex neurological diseases |
| Q30851786 | Insights into the mechanisms of absence seizure generation provided by EEG with functional MRI. |
| Q93225348 | Intellectual functioning and behavior in Dravet syndrome: A systematic review |
| Q50875144 | Interobserver agreement of the old and the newly proposed ILAE epilepsy classification in children. |
| Q48411945 | Intractable epilepsy secondary to cyclosporine toxicity in children undergoing allogeneic hematopoietic bone marrow transplantation |
| Q24234890 | Intravenous immunoglobulins for epilepsy |
| Q24235077 | Intravenous immunoglobulins for epilepsy |
| Q38694734 | Intravenous immunoglobulins for epilepsy. |
| Q34388967 | Investigating inhibitory control in children with epilepsy: an fMRI study |
| Q41647465 | Investigation of the possible association of NEDD4-2 (NEDD4L) gene with idiopathic photosensitive epilepsy |
| Q48156495 | Is colour modulation an independent factor in human visual photosensitivity? |
| Q36760356 | Is hypsarrhythmia a form of non-convulsive status epilepticus in infants? |
| Q34123660 | Is refractory epilepsy preventable? |
| Q47775840 | Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression. |
| Q51163786 | Jeavons syndrome in China. |
| Q88227140 | Juvenile myoclonic epilepsy refractory to treatment in a tertiary referral center |
| Q51867485 | Language deficits and altered hemispheric lateralization in young people in remission from BECTS. |
| Q48502724 | Language-induced epilepsy, acquired stuttering, and idiopathic generalized epilepsy: phenotypic study of one family |
| Q38892329 | Late Seizures after Stroke in Clinical Practice: The Prevalence of Non-convulsive Seizures |
| Q50657157 | Late-onset epileptic spasms: clinical evidence and outcome in 34 patients. |
| Q36496048 | Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy |
| Q36173584 | Lateralizing signs during seizures in focal epilepsy |
| Q21203654 | Lennox gastaut syndrome, review of the literature and a case report |
| Q34441873 | Lennox-Gastaut syndrome: a consensus approach to differential diagnosis |
| Q41510098 | Levetiracetam efficacy in children with epilepsy with electrical status epilepticus in sleep |
| Q24656333 | Levetiracetam in the treatment of epilepsy |
| Q43147847 | Levetiracetam, lamotrigine, and phenobarbital in patients with epileptic seizures and Alzheimer's disease |
| Q38422066 | Linguistic deficits following left selective amygdalohippocampectomy: a prospective study |
| Q48655789 | Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. |
| Q24642036 | Linkage and association analysis of CACNG3 in childhood absence epilepsy |
| Q41146397 | Localization of epileptic foci in Children with childhood absence epilepsy by magnetoencephalography combined with synthetic aperture magnetometry |
| Q97529194 | Location-specific reflex epilepsy: a novel reflex epilepsy phenotype |
| Q83178231 | Long term outcome in children affected by absence epilepsy with onset before the age of three years |
| Q34156070 | Long term outcome of temporal lobe epilepsy surgery: analyses of 140 consecutive patients |
| Q47851929 | Long-term follow-up of cognitive functions in patients with continuous spike-waves during sleep (CSWS). |
| Q44309995 | Long-term follow-up of patients with benign partial epilepsy in infancy |
| Q43061481 | Long-term outcome of 32 children with encephalopathy with status epilepticus during sleep, or ESES syndrome |
| Q48727972 | Long-term postoperative atrophy of contralateral hippocampus and cognitive function in unilateral refractory MTLE with unilateral hippocampal sclerosis |
| Q43886636 | Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy. |
| Q43049204 | Low plasma antioxidant status in patients with epilepsy and the role of antiepileptic drugs on oxidative stress |
| Q99609172 | Low-frequency Stimulation Decreases Hyperexcitability Through Adenosine A1 Receptors in the Hippocampus of Kindled Rats |
| Q48711666 | Magnetic resonance imaging abnormalities in children with epilepsy |
| Q43122262 | Magnetic resonance spectroscopy findings in photosensitive idiopathic generalized epilepsy |
| Q48768835 | Magnetoencephalographic analysis in children with Panayiotopoulos syndrome |
| Q47638832 | Major depressive episode, cognition, and epilepsy |
| Q35940537 | Mapping a mouse limbic seizure susceptibility locus on chromosome 10 |
| Q35216352 | Measuring the efficacy of antiepileptic drugs |
| Q37831588 | Mechanisms of epileptogenesis and potential treatment targets |
| Q37693139 | Medical management of Lennox-Gastaut syndrome |
| Q85296540 | Melatonin secretion in children with epilepsy |
| Q82639698 | Mesial temporal lobe epilepsy with hippocampal sclerosis: Study of 42 children |
| Q98244606 | Metabolic syndrome and obstructive sleep apnea syndrome among patients with epilepsy on monotherapy |
| Q38620937 | MicroRNA and mesial temporal lobe epilepsy with hippocampal sclerosis: Whole miRNome profiling of human hippocampus |
| Q54590725 | Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients. |
| Q91725421 | Microgliosis is associated with visual memory decline in patients with temporal lobe epilepsy and hippocampal sclerosis: A clinicopathologic study |
| Q37760082 | Migraine and epilepsy: a focus on overlapping clinical, pathophysiological, molecular, and therapeutic aspects |
| Q27012437 | Migraine in the borderland of epilepsy: "migralepsy" an overlapping syndrome of children and adults? |
| Q51966122 | Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. |
| Q89489899 | Molecular Aberrations Associated with Seizure Control in Diffuse Astrocytic and Oligodendroglial Tumors |
| Q64973430 | Molecular Mechanism Involved in the Pathogenesis of Early-Onset Epileptic Encephalopathy. |
| Q37286638 | Molecular and cellular basis of epileptogenesis in symptomatic epilepsy |
| Q26800090 | Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels |
| Q42025172 | Multi-electrode array study of neuronal cultures expressing nicotinic β2-V287L subunits, linked to autosomal dominant nocturnal frontal lobe epilepsy. An in vitro model of spontaneous epilepsy |
| Q90849351 | Multidisciplinary management improves anxiety, depression, medication adherence, and quality of life among patients with epilepsy in eastern China: A prospective study |
| Q48336116 | Multimodal MRI profiling of focal cortical dysplasia type II. |
| Q56740922 | Mutation analysis of WASF2 and GALE genes in one Chinese family with benign familial infantile convulsions with a novel locus |
| Q47810400 | Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes |
| Q37701079 | NaV1.1 channels and epilepsy |
| Q47941256 | Natural products as potential anticonvulsants: caffeoylquinic acids |
| Q37287002 | Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome. |
| Q37085097 | Navigating the channels and beyond: unravelling the genetics of the epilepsies |
| Q48489860 | Neck myoclonia with absence seizures: report of 3 cases |
| Q36344246 | Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+). |
| Q47772984 | Neonatal seizures and postneonatal epilepsy: a 7-y follow-up study. |
| Q38396781 | Neonatal seizures-part 1: Not everything that jerks, stiffens and shakes is a fit. |
| Q45083635 | Neurobehavior inventory: correlation with clinical aspects and quality of life in patients with epilepsy |
| Q34652317 | Neurobehavioral comorbidities of pediatric epilepsies are linked to thalamic structural abnormalities |
| Q38374909 | Neurobehavioral consequences of continuous spike and waves during slow sleep (CSWS) in a pediatric population: A pattern of developmental hindrance |
| Q35185047 | Neurodevelopment in new-onset juvenile myoclonic epilepsy over the first 2 years |
| Q33934907 | Neurodevelopmental alterations of large-scale structural networks in children with new-onset epilepsy |
| Q40406802 | Neuroimaging Evaluation for First Attack of Unprovoked Nonfebrile Seizure in Pediatrics: When to Order? |
| Q49037163 | Neuroimaging changes in mesial temporal lobe epilepsy are magnified in the presence of depression |
| Q40382374 | Neuronal networks in epileptic encephalopathies with CSWS. |
| Q38191248 | Neuropsychological approaches to epileptic encephalopathies |
| Q46618920 | Neuropsychological development in children belonging to BECTS spectrum: long-term effect of epileptiform activity |
| Q38680862 | Neuropsychological findings associated with Panayiotopoulos syndrome in three children |
| Q48485349 | Neuropsychological findings: myoclonic astatic epilepsy (MAE) and Lennox-Gastaut syndrome (LGS). |
| Q37693757 | New developments in the management of partial-onset epilepsy: role of brivaracetam |
| Q34504288 | New generation anticonvulsants for the treatment of epilepsy in children |
| Q46976276 | Newly treated epilepsy: a French observational study |
| Q36612676 | No relation between EFHC2 gene polymorphism and Idiopathic generalized epilepsy |
| Q38380950 | Non-invasive EEG evaluation in epilepsy diagnosis. |
| Q54082640 | Nonalcoholic fatty liver disease in adolescents receiving valproic acid. |
| Q46753522 | Nonconvulsive status epilepticus precipitated by carbamazepine presenting as dissociative and affective disorders in adolescents |
| Q33153322 | Nonepileptic disorders imitating generalized idiopathic epilepsies |
| Q34408411 | Occipital lobe epilepsy secondary to ulegyria |
| Q34755918 | Optimization of pilocarpine-mediated seizure induction in immunodeficient NodScid mice |
| Q36567996 | Outcome of paediatric convulsive status epilepticus: a systematic review. |
| Q37165872 | Outcomes of epilepsy surgery in adults and children |
| Q58800595 | Overnight Video-Polysomnographic Studies in Children with Intractable Epileptic Encephalopathies |
| Q34197693 | Overview: Idiopathic Generalized Epilepsies |
| Q74171093 | Panayiotopoulos syndrome |
| Q74219697 | Panayiotopoulos syndrome |
| Q42533556 | Panayiotopoulos syndrome in a child masquerading as septic shock |
| Q48474552 | Panayiotopoulos syndrome or early-onset benign childhood occipital epilepsy |
| Q36398768 | Panayiotopoulos syndrome: a consensus view |
| Q34620210 | Panayiotopoulos syndrome: a prospective study of 192 patients |
| Q48443273 | Panayiotopoulos syndrome: epidemiological and clinical characteristics and outcome |
| Q89858857 | Parental report of quality of life in children with epilepsy: A Spanish/French comparison |
| Q52123042 | Parents' perceptions of adversity introduced by upheaval and uncertainty at the onset of childhood epilepsy. |
| Q37540412 | Pathogenesis of epilepsy: challenges in animal models |
| Q30452365 | Pathophysiology and Definitions of Seizures and Status Epilepticus |
| Q38191243 | Pathophysiology of epileptic encephalopathies |
| Q33741436 | Patient-specific connectivity pattern of epileptic network in frontal lobe epilepsy |
| Q37061551 | Patterns of postictal cerebral perfusion in idiopathic generalized epilepsy: a multi-delay multi-parametric arterial spin labelling perfusion MRI study |
| Q44380019 | Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome |
| Q40749584 | Perspectives of epilepsy surgery in resource-poor countries: a study in Georgia. |
| Q34465801 | Pharmacologic management of convulsive status epilepticus in childhood |
| Q36404635 | Phenotype definition in epilepsy |
| Q35076345 | Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis |
| Q47649696 | Physical activity, stigma, and quality of life in patients with epilepsy |
| Q59222853 | Postpartum depression in women with epilepsy versus women without epilepsy |
| Q36007883 | Potential effects of valproate and oxcarbazepine on growth velocity and bone metabolism in epileptic children- a medical center experience |
| Q36319425 | Practical management issues for idiopathic generalized epilepsies |
| Q38026490 | Practices associated with serum antiepileptic drug level monitoring at a pediatric neurology clinic: a Malaysian experience. |
| Q36372571 | Practitioner review: use of antiepileptic drugs in children |
| Q47367341 | Predicting the likelihood of postoperative seizure status based on mRNA sequencing in low-grade gliomas |
| Q43710769 | Prediction for relapse and prognosis of newly diagnosed epilepsy |
| Q46445804 | Prediction of seizure outcome in childhood epilepsies in countries with limited resources: a prospective study |
| Q37155954 | Present status of surgical intervention for children with intractable seizures |
| Q43282721 | Prevalence of epilepsy and seizure disorders as causes of apparent life- threatening event (ALTE) in children admitted to a tertiary hospital |
| Q51911305 | Preventing depression in adolescents with epilepsy. |
| Q26995736 | Profile of once-daily zonisamide as monotherapy for treatment of partial seizures in adults |
| Q50701953 | Prognostic factors for outcome in pediatric probable lesional frontal lobe epilepsy with an unknown cause (cryptogenic). |
| Q92673537 | Prognostic factors in epileptic encephalopathies at onset in the first 2 years of life: The experience of a tertiary healthcare center in Italy |
| Q49239678 | Proprioceptive-Induced Reflex Postinfarct Seizures: A Rare Occurrence |
| Q45929795 | Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. |
| Q38906926 | Prospects of modeling poststroke epileptogenesis. |
| Q36372950 | Protein expression profiling of inflammatory mediators in human temporal lobe epilepsy reveals co-activation of multiple chemokines and cytokines |
| Q38040450 | Provoked and reflex seizures: surprising or common? |
| Q38866029 | Psychiatric and Neurocognitive Evaluation Focused on Frontal Lobe Functions in Rolandic Epilepsy |
| Q51892643 | Psychiatric comorbidity in adult patients with idiopathic generalized epilepsy. |
| Q35196841 | Psychiatric issues of childhood seizure disorders |
| Q46460391 | Quantitative HMRS and MRI volumetry indicate neuronal damage in the hippocampus of children with focal epilepsy and infrequent seizures |
| Q51874591 | Quantitative movement analysis differentiates focal seizures characterized by automatisms. |
| Q44339329 | RETRACTED: Association of mu-opioid receptor subunit gene and idiopathic generalized epilepsy |
| Q37618455 | Randomised clinical efficacy trial of topiramate and nitrazepam in treatment of infantile spasms |
| Q39000942 | Recent advances in epilepsy. |
| Q36153834 | Recovery of consciousness after epileptic seizures in children |
| Q81073721 | Recurrent autonomic status epilepticus in Panayiotopoulos syndrome: video/EEG studies |
| Q28585126 | Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy |
| Q91574974 | Reflex Seizures in a Patient with CDKL5 Deficiency Disorder |
| Q84668284 | Reflex absence epilepsy induced by gait |
| Q39764812 | Reflex reading epilepsy: effect of linguistic characteristics on spike frequency |
| Q38655924 | Reflex seizures, traits, and epilepsies: from physiology to pathology. |
| Q34432855 | Refractory grand mal seizures with onset during infancy including severe myoclonic epilepsy in infancy |
| Q80704085 | Refractory, life-threatening status epilepticus in a 3-year-old girl |
| Q34393533 | Relationship of number of seizures recorded on video-EEG to surgical outcome in refractory medial temporal lobe epilepsy |
| Q28264382 | Religiosity aspects in patients with epilepsy |
| Q34566789 | Report of the ILAE classification core group |
| Q33865523 | Response assessment in neuro-oncology (a report of the RANO group): assessment of outcome in trials of diffuse low-grade gliomas. |
| Q44278553 | Resting state basal ganglia network in idiopathic generalized epilepsy |
| Q35160999 | Risk factors for recurrence of epilepsy and withdrawal of antiepileptic therapy: a practical approach |
| Q49521735 | Role of Language-Related Functional Connectivity in Patients with Benign Childhood Epilepsy with Centrotemporal Spikes. |
| Q36507532 | Role of valproate across the ages. Treatment of epilepsy in children |
| Q53544790 | Rosmarinic acid exerts a neuroprotective effect in the kainate rat model of temporal lobe epilepsy: Underlying mechanisms. |
| Q40454564 | Safety and effectiveness of hormonal treatment versus hormonal treatment with vigabatrin for infantile spasms (ICISS): a randomised, multicentre, open-label trial. |
| Q48449484 | Screening of Inherited Metabolic Disorders in Infants with Infantile Spasms |
| Q48177180 | Seizure activity per se does not induce tissue damage markers in human neocortical focal epilepsy. |
| Q35696397 | Seizure characteristics and outcomes in 508 Chinese adult patients undergoing primary resection of low-grade gliomas: a clinicopathological study. |
| Q83792352 | Seizure control for patients undergoing meningioma surgery |
| Q51812792 | Seizures and epilepsy in Sotos syndrome: analysis of 19 Caucasian patients with long-term follow-up. |
| Q45339800 | Seizures and epilepsy in children |
| Q49075795 | Seizures and impairment of consciousness |
| Q48585257 | Seizures, syndromes, and etiologies in childhood epilepsy: The International League Against Epilepsy 1981, 1989, and 2017 classifications used in a population-based cohort |
| Q43556088 | Selective blockade of A(2A) receptor protects against neurotoxicity induced by kainic acid in young rats |
| Q33159108 | Semiologic aspects of epileptic seizures in 31 patients with hypothalamic hamartoma |
| Q37399575 | Semiology of epileptic seizures: a critical review |
| Q42144474 | Serum zinc level in children with simple febrile convulsions. |
| Q35546464 | Severe Myoclonic Epilepsy in Infancy - Adult Phenotype with Bradykinesia, Hypomimia, and Perseverative Behavior: Report of Five Cases |
| Q37861250 | Severe myoclonic epilepsy in infancy (Dravet syndrome) 30 years later |
| Q40521728 | Severe myoclonic epilepsy in infancy: toward an optimal treatment |
| Q35430460 | Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients |
| Q31104534 | Significance of miR-196b in tumor-related epilepsy of patients with gliomas |
| Q38679789 | Silencing of P2X7R by RNA interference in the hippocampus can attenuate morphological and behavioral impact of pilocarpine-induced epilepsy |
| Q44722863 | Sleep alterations in children with refractory epileptic encephalopathies: a polysomnographic study |
| Q34763997 | So what can we conclude--do seizures damage the brain? |
| Q39005710 | Social cognition dysfunctions in patients with epilepsy: Evidence from patients with temporal lobe and idiopathic generalized epilepsies. |
| Q93599749 | Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study |
| Q51942646 | Specific epileptic syndromes are rare even in tertiary epilepsy centers: a patient-oriented approach to epilepsy classification. |
| Q34177297 | Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. |
| Q39383450 | Spiritual/religious coping in patients with epilepsy: relationship with sociodemographic and clinical aspects and quality of life |
| Q37703950 | State of the Art Approach to the Classification of Epileptic Seizures and Epilepsies |
| Q92648627 | Status epilepticus in patients with genetic (idiopathic) generalized epilepsy |
| Q92113177 | Stigma, emotional aspects, and psychological symptoms in individuals with epilepsy |
| Q35874647 | Striatal hypertrophy and its cognitive effects in new-onset benign epilepsy with centrotemporal spikes |
| Q37290014 | Structural Abnormalities in Childhood Absence Epilepsy: Voxel-Based Analysis Using Diffusion Tensor Imaging |
| Q48574798 | Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test |
| Q47349167 | Study of seizure and epilepsy in Chinese children in Hong Kong: period prevalence and patterns |
| Q34319738 | Study on the Relationships between Intrinsic Functional Connectivity of the Default Mode Network and Transient Epileptic Activity. |
| Q44233533 | Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes |
| Q44846457 | Suicide attempts in adult patients with idiopathic generalized epilepsy |
| Q34501195 | Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients |
| Q90516390 | Surgery for epilepsy in the primary motor cortex: A critical review |
| Q38943285 | Surgical outcome in adolescents with mesial temporal sclerosis: Is it different? |
| Q92151990 | Sustained Effect of Botulinum Neurotoxin in Myoclonus Owing to Epilepsia Partialis Continua |
| Q46815996 | Symptomatic epilepsies imitating idiopathic generalized epilepsies |
| Q36319387 | Syndromes of idiopathic generalized epilepsies not recognized by the International League Against Epilepsy |
| Q92692047 | TMEM25 modulates neuronal excitability and NMDA receptor subunit NR2B degradation |
| Q33936438 | Tall gastrodis tuber combined with antiepileptic drugs repairs abnormal perfusion foci in focal epilepsy |
| Q37257128 | Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients. |
| Q47562691 | Targeting the Mammalian Target of Rapamycin for Epileptic Encephalopathies and Malformations of Cortical Development |
| Q35115219 | Tau reduction prevents disease in a mouse model of Dravet syndrome |
| Q30486496 | Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy |
| Q30419531 | Temporal lobe impairment in West syndrome: event-related potential evidence |
| Q35570181 | Text Classification towards Detecting Misdiagnosis of an Epilepsy Syndrome in a Pediatric Population |
| Q36005056 | Thalamocortical relationship in epileptic patients with generalized spike and wave discharges--A multimodal neuroimaging study |
| Q91581972 | The Analysis of Risk Factors and Survival Outcome for Chinese Patients with Epilepsy with High-Grade Glioma |
| Q48271595 | The ILAE classification of seizures and epilepsies: implications for the clinic |
| Q28554309 | The Natural History of Epilepsy in 163 Untreated Patients: Looking for "Oligoepilepsy" |
| Q36505024 | The TARC/sICAM5 Ratio in Patient Plasma is a Candidate Biomarker for Drug Resistant Epilepsy |
| Q37861252 | The core Dravet syndrome phenotype |
| Q37385054 | The economic burden of epilepsy in Korea, 2010. |
| Q35052172 | The effects of aqueous extract of Boswellia Serrata on hippocampal region CA1 and learning deficit in kindled rats |
| Q37965828 | The electroencephalogram of idiopathic generalized epilepsy |
| Q36883181 | The epidemiology of convulsive status epilepticus in children: a critical review. |
| Q37859417 | The etiologic classification of epilepsy |
| Q46328136 | The etiologic classification of epilepsy |
| Q90095454 | The evolution of the concepts of seizures and epilepsy: What's in a name? |
| Q90369478 | The features of neonatal seizures as predictors of drug-resistant epilepsy in children |
| Q38647365 | The forsaking of the clinical EEG by psychiatry: how justified? |
| Q35198044 | The genetics of human epilepsy |
| Q38191242 | The history of the concept of epileptic encephalopathy |
| Q35064294 | The ideal characteristics of antiepileptic therapy: an overview of old and new AEDs |
| Q35281782 | The importance of acknowledging clinical uncertainty in the diagnosis of epilepsy and non-epileptic events |
| Q41958955 | The importance of modeling epileptic seizure dynamics as spatio-temporal patterns |
| Q34775862 | The ketogenic diet for the treatment of childhood epilepsy: a randomised controlled trial |
| Q58449759 | The lifelong course of chronic epilepsy: the Chalfont experience |
| Q37037941 | The medical management of the epilepsies in children: conceptual and practical considerations. |
| Q36653787 | The natural history of myoclonic astatic epilepsy (Doose syndrome) and Lennox-Gastaut syndrome |
| Q50792570 | The neurophilosophy of epileptic experiences. |
| Q34224930 | The new ILAE report on terminology and concepts for organization of epileptic seizures: a clinician's critical view and contribution |
| Q37975513 | The new ILAE report on terminology and concepts for the organization of epilepsies: critical review and contribution |
| Q81884759 | The potential value of three-dimensional accelerometry for detection of motor seizures in severe epilepsy |
| Q30674774 | The promise of new antiepileptic drugs |
| Q38151433 | The quantitative measurement of consciousness during epileptic seizures |
| Q35560405 | The relationship between treatment with valproate, lamotrigine, and topiramate and the prognosis of the idiopathic generalised epilepsies. |
| Q38108310 | The role of epilepsy surgery in the treatment of childhood epileptic encephalopathy. |
| Q39332606 | The role of genetic testing in epilepsy diagnosis and management |
| Q48249670 | The spectrum of SCN1A-related infantile epileptic encephalopathies |
| Q36653791 | The spectrum of idiopathic Rolandic epilepsy syndromes and idiopathic occipital epilepsies: from the benign to the disabling |
| Q34311939 | The startle syndromes: physiology and treatment |
| Q34620620 | The syndrome of transient epileptic amnesia |
| Q33731012 | The therapeutic effect of the aqueous extract of boswellia serrata on the learning deficit in kindled rats |
| Q48445983 | The value of EEG-fMRI and EEG source analysis in the presurgical setup of children with refractory focal epilepsy |
| Q42677722 | The visual system in eyelid myoclonia with absences |
| Q38707353 | Theory of Mind in Patients with Epilepsy: a Systematic Review and Meta-analysis. |
| Q38191250 | Therapeutic approach to epileptic encephalopathies |
| Q37771378 | Therapeutic approaches to epileptogenesis--hope on the horizon |
| Q58800585 | Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study |
| Q58605690 | Transgenic overexpression of furin increases epileptic susceptibility |
| Q41488975 | Transplantation of bone marrow mononuclear cells modulates hippocampal expression of growth factors in chronically epileptic animals. |
| Q39990727 | Treatment of Lennox-Gastaut syndrome: overview and recent findings |
| Q37610185 | Treatment of epilepsies associated with typical absences |
| Q37236519 | Treatment of juvenile myoclonic epilepsy. |
| Q37129788 | Treatment of myoclonic seizures in patients with juvenile myoclonic epilepsy |
| Q38688752 | Treatment-resistant Lennox-Gastaut syndrome: therapeutic trends, challenges and future directions |
| Q94338261 | Treatments for the idiopathic occipital lobe epilepsies |
| Q48375427 | Triggers and techniques in termination of partial seizures |
| Q33152434 | Unconscious confusion--a literature search for definitions of syncope and related disorders |
| Q51921842 | Unusual features in eyelid myoclonia with absences: a patient with mild mental retardation and background slowing on electroencephalography. |
| Q26782070 | Update on diagnosis and management of childhood epilepsies |
| Q37906275 | Update on rufinamide in childhood epilepsy |
| Q37094135 | Use of chromosome substitution strains to identify seizure susceptibility loci in mice |
| Q37855043 | Use of peripheral blood transcriptome biomarkers for epilepsy prediction |
| Q99351942 | Use of the International League Against Epilepsy (ILAE) 1989, 2010, and 2017 Classification of Epilepsy in children in a low-resource setting: A hospital-based cross-sectional study |
| Q48774739 | Vagus nerve stimulation: effectiveness and tolerability in patients with epileptic encephalopathies |
| Q36445471 | Valproate as a mainstay of therapy for pediatric epilepsy |
| Q30826749 | Variable outcome for epilepsy after neonatal hypoglycaemia |
| Q35944595 | Ventricular enlargement in new-onset pediatric epilepsies |
| Q30371685 | Videopolygraphic and functional MRI study of musicogenic epilepsy. A case report and literature review. |
| Q34582636 | Vigabatrin for partial-onset seizure treatment in patients with tuberous sclerosis complex. |
| Q58319467 | Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial |
| Q46821821 | Visual cortex hyperexcitability in idiopathic generalized epilepsies with photosensitivity: a TMS pilot study |
| Q48299434 | Visual evoked potentials in children with occipital epilepsies |
| Q36286139 | Visual-sensitive epilepsies: classification and review |
| Q64063391 | Vitamin B12 and Folate Status in Patients with Epilepsy Under Levetiracetam Monotherapy |
| Q36525559 | Voltage-gated calcium channels and idiopathic generalized epilepsies. |
| Q33915194 | WONOEP appraisal: Molecular and cellular biomarkers for epilepsy |
| Q52015133 | Wavelet analysis of epileptic spikes. |
| Q53458719 | What do the suffixes - XR, ER, Chrono, Chronosphere - really mean as it pertains to modified-release antiepileptic drugs? |
| Q57905624 | What is at stake in a classification? |
| Q33519527 | What is new in paediatric epilepsy? |
| Q37955541 | What makes a simple partial seizure complex? |
| Q37102227 | What's new in: "genetics in childhood epilepsy". |
| Q35568655 | Why do seizures cause loss of consciousness? |
| Q48935129 | Writing epilepsy: a neurophysiological, neuropsychological and neuroimaging study |
| Q53938343 | [Antiepileptic drugs used in childhood. New products and new concepts] |
| Q83475203 | [Classification of epileptic seizures and syndromes] |
| Q73769732 | [Ictal signs--cerebral localization and propagation] |
| Q79840196 | [Suggestion for a new, patient-oriented epilepsy classification] |
| Q52023314 | [Typical absence seizure: epidemiological and clinical characteristics and outcome] |
| Q46507477 | fMRI functional networks for EEG source imaging |
| Q27303692 | hPSC-derived maturing GABAergic interneurons ameliorate seizures and abnormal behavior in epileptic mice |
| Q38668244 | microRNA and Epilepsy |
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