| Q38977472 | A Systematic Review of Psychiatric and Psychosocial Comorbidities of Genetic Generalised Epilepsies (GGE). |
| Q43665522 | Absence epilepsy with fast rhythmic discharges during sleep: an intermediary form of generalized epilepsy? |
| Q41835514 | Absences in juvenile myoclonic epilepsy: a clinical and video-electroencephalographic study |
| Q30697617 | Adolescent seizures and epilepsy syndromes |
| Q39010814 | Age-dependent Electroencephalographic Differences in the Genetic Absence Epilepsy Rats from Strasbourg (GAERS) Model of Absence Epilepsy |
| Q48466486 | Aggravation of generalized epilepsies |
| Q43545614 | Alteration of GLUR2 expression in the rat brain following absence seizures induced by gamma-hydroxybutyric acid |
| Q39038121 | Altered visual contrast gain control is sensitive for idiopathic generalized epilepsies |
| Q59619227 | Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy |
| Q33867724 | Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy |
| Q46725884 | Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy |
| Q34317995 | Basic mechanisms of generalized absence seizures |
| Q48947004 | Benign nocturnal childhood occipital epilepsy: a new syndrome with nocturnal seizures, tonic deviation of the eyes, and vomiting |
| Q38756516 | Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation |
| Q58417097 | Chapter 42 The idiopathic generalized epilepsies across life |
| Q28217195 | Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation |
| Q46850907 | Childhood absence epilepsy with clinically apparent genetic and acquired burdens: a diagnostic consideration |
| Q30835420 | Childhood absence epilepsy: genes, channels, neurons and networks. |
| Q48724501 | Classification of epilepsies and epileptic syndromes in two different samples of patients |
| Q48661466 | Consistent EEG focalities detected in subjects with primary generalized epilepsies monitored for two decades |
| Q35243852 | Contrast gain control abnormalities in idiopathic generalized epilepsy. |
| Q45195024 | Diagnosis and treatment of epilepsy |
| Q52026646 | Distinct behavioral and EEG topographic correlates of loss of consciousness in absences. |
| Q35679882 | Dysgraphia as a Mild Expression of Dystonia in Children with Absence Epilepsy |
| Q73179038 | EEG frequency profiles of idiopathic generalised epilepsy syndromes |
| Q33185889 | EEG in adult-onset idiopathic generalized epilepsy |
| Q31008127 | Electroencephalographic and neuroradiologic evaluation of children with epilepsy. |
| Q50547831 | Epidemiology of absence epilepsy. II. Typical absences in children with encephalopathies. |
| Q57086628 | Epilepsias generalizadas idiopáticas diagnosticadas incorretamente como epilepsias parciais |
| Q50895975 | Epilepsies in twins: genetics of the major epilepsy syndromes. |
| Q38608620 | Epilepsy: relationships between electrophysiology and intracellular mechanisms involving second messengers and gene expression |
| Q34254740 | Epileptic seizures and syndromes |
| Q39560707 | Epileptic syndromes in childhood |
| Q36879564 | Ethosuximide: from bench to bedside |
| Q67490956 | Evidence for GABAB-mediated mechanisms in experimental generalized absence seizures |
| Q57672617 | Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12 |
| Q52929662 | Exploration of the genetic architecture of idiopathic generalized epilepsies. |
| Q35857754 | Gamma-hydroxybutyric acid: neurobiology and toxicology of a recreational drug |
| Q51496878 | Ganaxolone, a selective, high-affinity steroid modulator of the gamma-aminobutyric acid-A receptor, exacerbates seizures in animal models of absence. |
| Q31030637 | Gelastic epilepsy. A clinical contribution |
| Q48166112 | Generalized absence seizures with 10-15 Hz fast discharges |
| Q33598113 | Genes and epilepsy |
| Q34086321 | Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies |
| Q44330504 | Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy |
| Q37470667 | Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. |
| Q57905570 | Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies |
| Q41626530 | Hereditary epilepsy syndromes. |
| Q48271806 | Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathy |
| Q39712905 | Hypothalamic hamartomas and ictal laughter: Evolution of a characteristic epileptic syndrome and diagnostic value of magnetic resonance imaging |
| Q43630082 | Ictal single photon emission computed tomography in absence seizures: apparent implication of different neuronal mechanisms |
| Q58417142 | Idiopathic Generalized Epilepsies: Do Sporadic and Familial Cases Differ? |
| Q36317373 | Idiopathic generalised epilepsy in adults manifested by phantom absences, generalised tonic-clonic seizures, and frequent absence status |
| Q48765141 | Idiopathic generalized epilepsies with versive or circling seizures |
| Q37496002 | Idiopathic generalized epilepsy (IGE) syndromes in development: IGE with absences of early childhood, IGE with phantom absences, and perioral myoclonia with absences |
| Q34301392 | Idiopathic generalized epilepsy with generalized and other seizures in adolescence |
| Q52222664 | Infant onset subacute necrotizing encephalomyelopathy (Leigh's disease) |
| Q40570288 | Inherited epilepsies of childhood |
| Q33961512 | Is epilepsy a progressive disease? The neurobiological consequences of epilepsy |
| Q54474174 | Late onset absence seizures in multiple sclerosis: a case report. |
| Q52979774 | Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy. |
| 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 |
| Q80903720 | Long-term prognosis for childhood and juvenile absence epilepsy |
| Q28216597 | Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy |
| Q34154771 | Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy |
| Q37085097 | Navigating the channels and beyond: unravelling the genetics of the epilepsies |
| Q52955807 | No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1. |
| Q52955275 | No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures. |
| Q43876599 | Nonconvulsive status epilepticus in adults: thirty-two consecutive patients from a general hospital population |
| Q48461890 | Pathophysiological mechanisms of genetic absence epilepsy in the rat. |
| Q40961005 | Pediatric epilepsy syndromes: an update and critical review |
| Q81632341 | Perioral myoclonia with absences: an overlooked and misdiagnosed generalized seizure type |
| Q48666440 | Perioral myoclonia with absences? A case report with EEG and voltage mapping analysis |
| Q42655007 | Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME. |
| Q37196957 | Polyspike and waves do not predict generalized tonic-clonic seizures in childhood absence epilepsy |
| Q98226478 | Polyspike ictal-onset absence seizures in a pediatric patient with Down syndrome |
| Q73592109 | Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies |
| Q36319425 | Practical management issues for idiopathic generalized epilepsies |
| Q48820789 | Proton magnetic resonance spectroscopic imaging for discrimination of absence and complex partial seizures |
| Q48386865 | Relations between cortical and thalamic cellular activities during absence seizures in rats |
| Q81665395 | Relationships within the idiopathic generalized epilepsies |
| Q40781638 | Some aspects of prognosis in the epilepsies: a review |
| Q52037328 | Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorder. |
| Q73443703 | The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han population |
| Q42673049 | The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy |
| Q51731141 | The ontogeny of GABAergic enhancement of the gamma-hydroxybutyrate model of generalized absence seizures. |
| Q72007203 | The phenotypic spectrum related to the human epilepsy susceptibility gene “EJM1” |
| Q51052566 | Two forms of déjà vu experiences in patients with epilepsy. |
| Q34892554 | Typical absence seizures and related epileptic syndromes: assessment of current state and directions for future research |
| Q33591987 | Typical absence seizures in adults: clinical, EEG, video-EEG findings and diagnostic/syndromic considerations |
| Q42688492 | Typical absence status in adults: diagnostic and syndromic considerations |
| Q34254748 | Use of routine and video electroencephalography |
| Q52970675 | Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy. |
| Q74076149 | [Status epilepticus with confusional symptomatology] |
| Q51770099 | gamma-Hydroxybutyrate model of generalized absence seizures: further characterization and comparison with other absence models. |