Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scn1b-based model of Dravet syndrome

De novo mutations in epileptic encephalopathies

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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

(2013) Gemma L Carvill et al.   NATURE GENETICS

Multiple molecular mechanisms for a single GABAA mutation in epilepsy

(2013) C. A. Reid et al.   NEUROLOGY

Abnormal neuronal patterning occurs during early postnatal brain development of Scn1b-null mice and precedes hyperexcitability

(2013) W. J. Brackenbury et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Progressive Gait Deterioration in Adolescents With Dravet Syndrome

(2012) Jill M. Rodda et al.   ARCHIVES OF NEUROLOGY

Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome

(2012) Dezhi Cao et al.   EPILEPSIA

The mechanism of action of retigabine (ezogabine), a first-in-class K+ channel opener for the treatment of epilepsy

(2012) Martin J. Gunthorpe et al.   EPILEPSIA

The spectrum of anticonvulsant efficacy of retigabine (ezogabine) in animal models: Implications for clinical use

(2012) Charles H. Large et al.   EPILEPSIA

A homozygous mutation of voltage-gated sodium channel βIgeneSCN1Bin a patient with Dravet syndrome

(2012) Ikuo Ogiwara et al.   EPILEPSIA

NontruncatingSCN1AMutations Associated with Severe Myoclonic Epilepsy of Infancy Impair Cell Surface Expression

(2012) Christopher H. Thompson et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Sodium Channel Accessory Subunit Nav 1 Regulates Neuronal Excitability through Modulation of Repolarizing Voltage-Gated K+ Channels

(2012) C. Marionneau et al.   JOURNAL OF NEUROSCIENCE

Aberrant Dendritic Excitability: A Common Pathophysiology in CNS Disorders Affecting Memory?

(2012) Michael W. Nestor et al.   MOLECULAR NEUROBIOLOGY

Closed-loop optogenetic control of thalamus as a tool for interrupting seizures after cortical injury

(2012) Jeanne T Paz et al.   NATURE NEUROSCIENCE

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome

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

The pharmacologic treatment of Dravet syndrome

(2011) Catherine Chiron et al.   EPILEPSIA

The effects of stiripentol on GABAA receptors

(2011) Janet L. Fisher   EPILEPSIA

Voltage-Gated Na+ Channel  1B: A Secreted Cell Adhesion Molecule Involved in Human Epilepsy

(2011) G. A. Patino et al.   JOURNAL OF NEUROSCIENCE

Glutamatergic pre-ictal discharges emerge at the transition to seizure in human epilepsy

(2011) Gilles Huberfeld et al.   NATURE NEUROSCIENCE

Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotype

(2011) Mario Mastrangelo et al.   PEDIATRIC NEUROLOGY

Na+ Channel ? Subunits: Overachievers of the Ion Channel Family

(2011) William J. Brackenbury et al.   Frontiers in Pharmacology

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

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

Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus

(2010) Verena C. Wimmer et al.   JOURNAL OF CLINICAL INVESTIGATION

Kv7 (KCNQ) channel openers induce hypothermia in the mouse

(2010) Line V. Kristensen et al.   NEUROSCIENCE LETTERS

Functional reciprocity between Na+ channel Nav1.6 and  1 subunits in the coordinated regulation of excitability and neurite outgrowth

(2010) W. J. Brackenbury et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Translational Research in Epilepsy Genetics

(2009) Saul A. Mullen et al.   ARCHIVES OF NEUROLOGY

A Functional Null Mutation of SCN1B in a Patient with Dravet Syndrome

(2009) G. A. Patino et al.   JOURNAL OF NEUROSCIENCE

A revised Racine's scale for PTZ-induced seizures in rats

(2009) Annika Lüttjohann et al.   PHYSIOLOGY & BEHAVIOR

Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy

(2009) J. C. Oakley et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Increased thalamic inhibition in the absence seizure prone DBA/2J mouse

(2008) Heneu O. Tan et al.   EPILEPSIA

Voltage-Gated Na+ Channel  1 Subunit-Mediated Neurite Outgrowth Requires Fyn Kinase and Contributes to Postnatal CNS Development In Vivo

(2008) W. J. Brackenbury et al.   JOURNAL OF NEUROSCIENCE

Mechanisms of human inherited epilepsies

(2008) Christopher A. Reid et al.   PROGRESS IN NEUROBIOLOGY

Severe myoclonic epilepsy in infancy: A systematic review and a meta-analysis of individual patient data

(2007) Behrouz Kassaï et al.   EPILEPSIA