Epilepsia

Complete Loss of the Cytoplasmic Carboxyl Terminus of the KCNQ2 Potassium Channel: A Novel Mutation in a Large Czech Pedigree with Benign Neonatal Convulsions or Other Epileptic Phenotypes

"A Follow-up Survey on Seizures Induced by Animated Cartoon TV Program ""Pocket Monster"

Bilateral Hippocampal Volume Loss in Patients with a History of Encephalitis or Meningitis

Benzodiazepine-GABA

Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the

AUFGABEN UND ZIELE DER EPILEPSIE-FORSCHUNG.

An Xp; Yq Translocation Causing a Novel Contiguous Gene Syndrome in Brothers with Generalized Epilepsy, Ichthyosis, and Attention Deficits

An Incident Case-Control Study of First Unprovoked Afebrile Seizures in Children: A Population-Based Study of Pre- and Perinatal Risk Factors

Advances in Understanding the Process of Epileptogenesis Based on Patient Material: What Can the Patient Tell Us?

Absence Epilepsy with Onset before Age Three Years: Could this Be Glut-1 Deficiency Syndrome (De Vivo Syndrome)?

A Pharmacoepidemiologic Study of Factors Influencing the Outcome of Treatment with Lamotrigine in Chronic Epilepsy

A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood-onset Cognitive Deficit