Co-occurring malformations of cortical development andSCN1Agene mutations

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene

(2013) Valerio Conti et al.   BRAIN

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

(2013) Eija Gaily et al.   EPILEPSIA

Progressive Gait Deterioration in Adolescents With Dravet Syndrome

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

A developmental and genetic classification for malformations of cortical development: update 2012

(2012) A. James Barkovich et al.   BRAIN

Dysfunction of KCNK Potassium Channels Impairs Neuronal Migration in the Developing Mouse Cerebral Cortex

(2012) Yuki Bando et al.   CEREBRAL CORTEX

Dravet syndrome: The main issues

(2012) Renzo Guerrini   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

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

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

Status epilepticus-induced pathologic plasticity in a rat model of focal cortical dysplasia

(2011) Francesca Colciaghi et al.   BRAIN

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

(2011) C. B. Catarino et al.   BRAIN

Insights into pathophysiology and therapy from a mouse model of Dravet syndrome

(2011) John C. Oakley et al.   EPILEPSIA

Neuroimaging and neuropathology of Dravet syndrome

(2011) Renzo Guerrini et al.   EPILEPSIA

The core Dravet syndrome phenotype

(2011) Charlotte Dravet   EPILEPSIA

De novo SCN1A mutations in migrating partial seizures of infancy

(2011) D. Carranza Rojo et al.   NEUROLOGY

Genotype-phenotype associations in SCN1A-related epilepsies

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

Role of cortical dysplasia in epileptogenesis following prolonged febrile seizure

(2010) Kyung-Il Park 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

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

(2010) C. Depienne et al.   JOURNAL OF MEDICAL GENETICS

NaV1.1 channels and epilepsy

(2010) William A. Catterall et al.   JOURNAL OF PHYSIOLOGY-LONDON

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

(2009) Carla Marini et al.   EPILEPSIA

A long-term follow-up study of Dravet syndrome up to adulthood

(2009) Mari Akiyama et al.   EPILEPSIA

HYPONATREMIA IN NEUROSURGICAL PATIENTS

(2009) Maryam Rahman et al.   NEUROSURGERY

Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options

(2008) Renzo Guerrini et al.   TRENDS IN NEUROSCIENCES