Published in Epilepsia on December 01, 2006
The immature dentate gyrus represents a shared phenotype of mouse models of epilepsy and psychiatric disease. Bipolar Disord (2013) 0.92
Hippocampal physiology, structure and function and the neuroscience of schizophrenia: a unified account of declarative memory deficits, working memory deficits and schizophrenic symptoms. Behav Sci (Basel) (2013) 0.83
Postictal psychosis: common, dangerous, and treatable. Epilepsy Curr (2008) 0.82
The postictal state: effects of age and underlying brain dysfunction. Epilepsy Behav (2010) 0.78
Neuroimaging of frontal-limbic dysfunction in schizophrenia and epilepsy-related psychosis: toward a convergent neurobiology. Epilepsy Behav (2011) 0.78
Treatment strategies in the postictal state. Epilepsy Behav (2010) 0.78
A change in electrographic activity and blood flow during interictal and postictal psychotic states in a patient with epilepsy. Epilepsy Behav Case Rep (2015) 0.75
Hospital care for mental health and substance abuse in children with epilepsy. Epilepsy Behav (2016) 0.75
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures. Brain (2003) 2.44
A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline. J Neurosci (2004) 2.31
Long-term course of Dravet syndrome: a study from an epilepsy center in Japan. Epilepsia (2014) 1.99
Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet (2004) 1.98
Autoantibodies and cell-mediated autoimmunity to NMDA-type GluRepsilon2 in patients with Rasmussen's encephalitis and chronic progressive epilepsia partialis continua. Epilepsia (2005) 1.65
The effect of scatter correction on 123I-IMP brain perfusion SPET with the triple energy window method in normal subjects using SPM analysis. Eur J Nucl Med Mol Imaging (2002) 1.45
A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy. Neurobiol Dis (2006) 1.45
Intracranial EEG findings in patients with lesional lateral temporal lobe epilepsy. Epilepsy Res (2008) 1.44
Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents. Epilepsy Res (2003) 1.42
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online. Hum Mutat (2007) 1.03
Risk factors for hyperammonemia associated with valproic acid therapy in adult epilepsy patients. Epilepsy Res (2012) 1.03
A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome. Epilepsia (2012) 1.01
Contribution of subtraction ictal SPECT coregistered to MRI to epilepsy surgery: a multicenter study. Ann Nucl Med (2009) 0.99
[Rasmussen encephalitis and non-herpetic acute limbic encephalitis]. Rinsho Shinkeigaku (2008) 0.95
HLA class I markers in Japanese patients with carbamazepine-induced cutaneous adverse reactions. Epilepsia (2009) 0.95
Comparison of neuropsychological outcomes after selective amygdalohippocampectomy versus anterior temporal lobectomy. Epilepsy Behav (2006) 0.94
Rapid amygdala gamma oscillations in response to fearful facial expressions. Neuropsychologia (2010) 0.93
Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood. Brain Dev (2013) 0.92
Risk factors for hyperammonemia in pediatric patients with epilepsy. Epilepsia (2013) 0.91
Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation. Epilepsy Res (2007) 0.90
Role of primary sensorimotor cortex and supplementary motor area in volitional swallowing: a movement-related cortical potential study. Am J Physiol Gastrointest Liver Physiol (2003) 0.90
Involvement of medial temporal structures in reflexive attentional shift by gaze. Soc Cogn Affect Neurosci (2007) 0.89
Mortality in Dravet syndrome: search for risk factors in Japanese patients. Epilepsia (2011) 0.88
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population. J Hum Genet (2005) 0.88
Ictal very low frequency oscillation in human epilepsy patients. Ann Neurol (2010) 0.87
Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome. Epilepsia (2011) 0.87
Modulation of epileptiform EEG discharges in juvenile myoclonic epilepsy: an investigation of reflex epileptic traits. Epilepsia (2012) 0.87
Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome. Hum Mutat (2010) 0.87
Rapid amygdala gamma oscillations in response to eye gaze. PLoS One (2011) 0.86
Clinical significance of ictal high frequency oscillations in medial temporal lobe epilepsy. Clin Neurophysiol (2011) 0.86
A substantial number of Rasmussen syndrome patients have increased IgG, CD4+ T cells, TNFalpha, and Granzyme B in CSF. Epilepsia (2009) 0.86
Percutaneous angioplasty of a chronic total occlusion of the intracranial internal carotid artery. Case report. Surg Neurol (2006) 0.85
Influence of CYP2C19 polymorphism and concomitant antiepileptic drugs on serum clobazam and N-desmethyl clobazam concentrations in patients with epilepsy. Ther Drug Monit (2013) 0.84
Development of multi-dimensional action checklist for promoting new approaches in participatory occupational safety and health in small and medium-sized enterprises. Ind Health (2006) 0.84
Temporal profile of amygdala γ oscillations in response to faces. J Cogn Neurosci (2011) 0.84
Gamma knife radiosurgery for cavernous sinus metastases and invasion. Surg Neurol (2005) 0.83
Very high frequency oscillations (over 1000 Hz) in human epilepsy. Clin Neurophysiol (2010) 0.83
Multi-center study on post-ictal headache in patients with localization-related epilepsy. Psychiatry Clin Neurosci (2003) 0.83
Lamotrigine is favourable for startle-induced seizures. Epileptic Disord (2011) 0.83
KCC2 was downregulated in small neurons localized in epileptogenic human focal cortical dysplasia. Epilepsy Res (2011) 0.82
Usefulness of 123I-iomazenil single-photon emission computed tomography in discriminating between mesial and lateral temporal lobe epilepsy in patients in whom magnetic resonance imaging demonstrates normal findings. J Neurosurg (2007) 0.82
Very high-frequency oscillations (over 1000 Hz) of somatosensory-evoked potentials directly recorded from the human brain. J Clin Neurophysiol (2009) 0.82
Influence of concomitant antiepileptic drugs on plasma lamotrigine concentration in adult Japanese epilepsy patients. Biol Pharm Bull (2012) 0.82
Uneven interhemispheric connections between left and right primary sensori-motor areas. Hum Brain Mapp (2011) 0.81
[Acute limbic encephalitis and NMDA type-glutamate receptor]. Rinsho Shinkeigaku (2008) 0.81
Gamma knife radiosurgery for growth hormone-producing adenomas. J Clin Neurosci (2010) 0.81
Intracerebral cavernous malformation induced by radiosurgery. Case report. Neurol Med Chir (Tokyo) (2007) 0.80
Vaccination and infection as causative factors in Japanese patients with Rasmussen syndrome: molecular mimicry and HLA class I. Clin Dev Immunol (2006) 0.80
Long-term seizure outcome following resective surgery at National Epilepsy Center in Shizuoka, Japan. Psychiatry Clin Neurosci (2004) 0.80
Mesial temporal lobe epilepsy with no specific histological abnormality: a distinct surgically remediable syndrome. Epilepsy Behav (2013) 0.80
Influence of uridine diphosphate glucuronosyltransferase 2B7 -161C>T polymorphism on the concentration of valproic acid in pediatric epilepsy patients. Ther Drug Monit (2014) 0.79
Rapid and multiple-stage activation of the human amygdala for processing facial signals. Commun Integr Biol (2013) 0.79
Neural connection between bilateral basal temporal regions: cortico-cortical evoked potential analysis in patients with temporal lobe epilepsy. Neurosurgery (2009) 0.79
Generators of tibial nerve somatosensory evoked potential: recorded from the mesial surface of the human brain using subdural electrodes. J Clin Neurophysiol (2009) 0.79
Early seizure propagation from the occipital lobe to medial temporal structures and its surgical implication. Epileptic Disord (2008) 0.79
Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome. Epilepsia (2012) 0.79