Altered sleep regulation in a mouse model ofSCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+)

NaV1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythms

(2012) S. Han et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Control of hippocampal theta rhythm by serotonin: Role of 5-HT2c receptors

(2011) Elin Sörman et al.   NEUROPHARMACOLOGY

Scn1a missense mutation impairs GABAA receptor-mediated synaptic transmission in the rat hippocampus

(2010) Yukihiro Ohno et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy

(2010) Premysl Jiruska et al.   BRAIN

GABAergic neurons intermingled with orexin and MCH neurons in the lateral hypothalamus discharge maximally during sleep

(2010) Oum Kaltoum Hassani et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Dysfunction of theScn8aVoltage-gated Sodium Channel Alters Sleep Architecture, Reduces Diurnal Corticosterone Levels, and Enhances Spatial Memory

(2010) Ligia A. Papale et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Altered Function of theSCN1AVoltage-gated Sodium Channel Leads to γ-Aminobutyric Acid-ergic (GABAergic) Interneuron Abnormalities

(2010) Melinda S. Martin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

(2009) Xiuyu Shi et al.   BRAIN & DEVELOPMENT

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

(2009) Ligia A. Papale et al.   HUMAN MOLECULAR GENETICS

The genetic and molecular regulation of sleep: from fruit flies to humans

(2009) Chiara Cirelli   NATURE REVIEWS NEUROSCIENCE

De novo mutations of voltage-gated sodium channel  II gene SCN2A in intractable epilepsies

(2009) I. Ogiwara et al.   NEUROLOGY

Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A

(2009) Krista Mahoney et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

First Mutation in the Voltage-Gated Nav1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy

(2008) M-J Castro et al.   CEPHALALGIA

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation

(2008) Neeti Hindocha et al.   EPILEPSIA

An unexpected EEG course in Dravet syndrome

(2008) Rima Nabbout et al.   EPILEPSY RESEARCH

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

(2008) Katherine D. Holland et al.   NEUROSCIENCE LETTERS