Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy

Co-occurring malformations of cortical development andSCN1Agene mutations

(2014) Carmen Barba et al.   EPILEPSIA

Mesial Temporal Sclerosis in a Cohort of Children With SCN1A Gene Mutation

(2012) Katherine Van Poppel et al.   JOURNAL OF CHILD NEUROLOGY

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

(2011) C. B. Catarino et al.   BRAIN

Neuroimaging and neuropathology of Dravet syndrome

(2011) Renzo Guerrini et al.   EPILEPSIA

The core Dravet syndrome phenotype

(2011) Charlotte Dravet   EPILEPSIA

The genetics of Dravet syndrome

(2011) Carla Marini et al.   EPILEPSIA

A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation

(2010) François Le Gal et al.   EPILEPSIA

The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1

(2010) Ingmar Blümcke et al.   EPILEPSIA

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Interobserver and intraobserver reproducibility in focal cortical dysplasia (malformations of cortical development)

(2009) Wendy A. Chamberlain et al.   EPILEPSIA

Different features of histopathological subtypes of pediatric focal cortical dysplasia

(2008) Pavel Krsek et al.   ANNALS OF NEUROLOGY

DoSCN1Amutations protect from hippocampal sclerosis?

(2008)   EPILEPSIA