Dravet syndrome in Sweden: a population-based study

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

(2014) Rumiko Takayama et al.   EPILEPSIA

GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome

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

Progressive Gait Deterioration in Adolescents With Dravet Syndrome

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

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

(2012) A. Brunklaus et al.   BRAIN

PCDH19-related infantile epileptic encephalopathy: An unusual X-linked inheritance disorder

(2012) Christel Depienne et al.   HUMAN MUTATION

Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants

(2011) RENZO GUERRINI et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Electroencephalographic characteristics of Dravet syndrome

(2011) Michelle Bureau et al.   EPILEPSIA

Neuroimaging and neuropathology of Dravet syndrome

(2011) Renzo Guerrini 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 core Dravet syndrome phenotype

(2011) Charlotte Dravet   EPILEPSIA

The genetics of Dravet syndrome

(2011) Carla Marini et al.   EPILEPSIA

Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: A prospective pilot study

(2011) Rima Nabbout et al.   EPILEPSIA

Electroencephalographic Features in Dravet Syndrome

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

Genotype-phenotype associations in SCN1A-related epilepsies

(2011) S. M. Zuberi et al.   NEUROLOGY

Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene

(2010) Renzo Guerrini et al.   EPILEPSIA

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

The International Classification of Diseases, 10th Edition (ICD-10) changeover is coming

(2010)   OPTOMETRY

Dravet syndrome: Early clinical manifestations and cognitive outcome in 37 Italian patients

(2009) Francesca Ragona et al.   BRAIN & DEVELOPMENT

SCN1Aduplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

(2009) Carla Marini et al.   EPILEPSIA

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

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

(2008) C Depienne et al.   JOURNAL OF MEDICAL GENETICS

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

(2007) Behrouz Kassaï et al.   EPILEPSIA