Neuroimaging and neuropathology of Dravet syndrome

The genetics of Dravet syndrome

(2011) Carla Marini et al.   EPILEPSIA

Polymicrogyria and epilepsy

(2010) Renzo Guerrini   EPILEPSIA

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

(2010) François Le Gal et al.   EPILEPSIA

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

(2010) Renzo Guerrini et al.   EPILEPSIA

Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene

(2010) A. Suls et al.   NEUROLOGY

Unusual consequences of status epilepticus in Dravet syndrome

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

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

(2009) Carla Marini et al.   EPILEPSIA

Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy

(2009) Takafumi Sakakibara et al.   EPILEPSIA

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

(2009) Mari Akiyama et al.   EPILEPSIA

Rasmussen encephalitis associated withSCN1Amutation

(2007) Iori Ohmori et al.   EPILEPSIA