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

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

(2011) C. B. Catarino et al.   BRAIN

A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome

(2011) Blanca Tro-Baumann et al.   EPILEPSIA

Encephalopathy and SCN1A mutations

(2011) Shan Tang 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

Comorbidities and predictors of health-related quality of life in Dravet syndrome

(2011) Andreas Brunklaus et al.   EPILEPSIA

Genotype-phenotype associations in SCN1A-related epilepsies

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

Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report

(2010) Masaru Takayanagi et al.   EPILEPSIA

Investigation of widespread neocortical pathology associated with hippocampal sclerosis in epilepsy: A postmortem study

(2010) Francine Blanc et al.   EPILEPSIA

Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study

(2010) Anne M McIntosh et al.   LANCET NEUROLOGY

Long-Term Mortality in Childhood-Onset Epilepsy

(2010) Matti Sillanpää et al.   NEW ENGLAND JOURNAL OF MEDICINE

Unusual consequences of status epilepticus in Dravet syndrome

(2010) M. Chipaux et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Levetiracetam in Childhood Epilepsy

(2010) Alberto Verrotti et al.   PEDIATRIC DRUGS

Translational Research in Epilepsy Genetics

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

TheSCN1Avariant database: a novel research and diagnostic tool

(2009) Lieve RF Claes et al.   HUMAN MUTATION

Physicochemical property changes of amino acid residues that accompany missense mutations in SCN1A affect epilepsy phenotype severity

(2009) K Kanai et al.   JOURNAL OF MEDICAL 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 catalog of SCN1A variants

(2008) Christoph Lossin   BRAIN & DEVELOPMENT

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

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

Refractory, life-threatening status epilepticus in a 3-year-old girl

(2008) Pasquale Striano et al.   LANCET NEUROLOGY