Dravet Syndrome: Diagnosis and Long-Term Course

Ictal ontogeny in Dravet syndrome

(2015) Se Hee Kim et al.   CLINICAL NEUROPHYSIOLOGY

The incidence ofSCN1A-related Dravet syndrome in Denmark is 1:22,000: A population-based study from 2004 to 2009

(2015) Allan Bayat et al.   EPILEPSIA

Co-occurring malformations of cortical development andSCN1Agene mutations

(2014) Carmen Barba et al.   EPILEPSIA

Long-term course of Dravet syndrome: A study from an epilepsy center in Japan

(2014) Rumiko Takayama et al.   EPILEPSIA

Cognitive and adaptive evaluation of 21 consecutive patients with Dravet syndrome

(2014) Nathalie Villeneuve et al.   EPILEPSY & BEHAVIOR

Brain morphometry of Dravet Syndrome

(2014) Alejandro Pérez et al.   EPILEPSY RESEARCH

Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome

(2014) A. Fasano et al.   NEUROLOGY

GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome

(2014) G. L. Carvill et al.   NEUROLOGY

Sleep Abnormalities in Children With Dravet Syndrome

(2014) Radhika Dhamija et al.   PEDIATRIC NEUROLOGY

Untangling the Dravet Syndrome Seizure Network: The Changing Face of a Rare Genetic Epilepsy

(2014) Ravi Chopra et al.   Epilepsy Currents

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

(2013) Arvid Suls et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations

(2013) Xiaojing Xu et al.   BRAIN & DEVELOPMENT

Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome

(2013) Christine S Cheah et al.   Channels

SCN1Atesting for epilepsy: Application in clinical practice

(2013) Shinichi Hirose et al.   EPILEPSIA

Dravet syndrome: New potential genetic modifiers, imaging abnormalities, and ictal findings

(2013) Eija Gaily et al.   EPILEPSIA

Role of the sodium channelSCN9Ain genetic epilepsy with febrile seizures plus and Dravet syndrome

(2013) John C. Mulley et al.   EPILEPSIA

Transition and transfer from pediatric to adult health care in epilepsy: A families' survey on Dravet syndrome

(2013) Mathieu Kuchenbuch et al.   EPILEPSY & BEHAVIOR

Sudden unexpected death in a mouse model of Dravet syndrome

(2013) Franck Kalume et al.   JOURNAL OF CLINICAL INVESTIGATION

Focal Scn1a knockdown induces cognitive impairment without seizures

(2013) Alex C. Bender et al.   NEUROBIOLOGY OF DISEASE

Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy

(2013) Rima Nabbout et al.   Orphanet Journal of Rare Diseases

Altered Cardiac Electrophysiology and SUDEP in a Model of Dravet Syndrome

(2013) David S. Auerbach et al.   PLoS One

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome

(2012) A. Brunklaus et al.   BRAIN

Autistic-like behaviour in Scn1a +/− mice and rescue by enhanced GABA-mediated neurotransmission

(2012) Sung Han et al.   NATURE

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

(2012) Iori Ohmori et al.   NEUROBIOLOGY OF DISEASE

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

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

(2011) C. B. Catarino et al.   BRAIN

Dravet syndrome: The long-term outcome

(2011) Pierre Genton et al.   EPILEPSIA

Dravet syndrome and parent associations: The IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief

(2011) Joan V. Skluzacek et al.   EPILEPSIA

The genetics of Dravet syndrome

(2011) Carla Marini et al.   EPILEPSIA

Neuropsychological development in children with Dravet syndrome

(2011) Daniela Chieffo et al.   EPILEPSY RESEARCH

Electroencephalographic Features in Dravet Syndrome

(2011) Nicola Specchio et al.   JOURNAL OF CHILD NEUROLOGY

Early development in Dravet syndrome; visual function impairment precedes cognitive decline

(2010) Daniela Chieffo et al.   EPILEPSY RESEARCH

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

(2009) Nanda A. Singh et al.   PLoS Genetics

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

(2009) Christel Depienne et al.   PLoS Genetics

A Screening test for the prediction of Dravet syndrome before one year of age

(2008) Junri Hattori et al.   EPILEPSIA

An unexpected EEG course in Dravet syndrome

(2008) Rima Nabbout et al.   EPILEPSY RESEARCH