Severe Epilepsy Syndromes of Early Childhood: The Link Between Genetics and Pathophysiology With a Focus on SCN1A Mutations

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

(2009) Ingrid E. Scheffer et al.   BRAIN & DEVELOPMENT

Epileptic syndromes in infancy and childhood

(2009) Rima Nabbout et al.   CURRENT OPINION IN NEUROLOGY

A catalog of SCN1A variants

(2008) Christoph Lossin   BRAIN & DEVELOPMENT

How do mutant Nav1.1 sodium channels cause epilepsy?

(2008) David S. Ragsdale   BRAIN RESEARCH REVIEWS

Inherited Neuronal Ion Channelopathies: New Windows on Complex Neurological Diseases

(2008) W. A. Catterall et al.   JOURNAL OF NEUROSCIENCE

Navigating the channels and beyond: unravelling the genetics of the epilepsies

(2008) Ingo Helbig et al.   LANCET NEUROLOGY

Mechanisms of human inherited epilepsies

(2008) Christopher A. Reid et al.   PROGRESS IN NEUROBIOLOGY

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

(2007) Behrouz Kassaï et al.   EPILEPSIA