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Novel Mutation in KCNQ2 Causing Benign Familial Neonatal Seizures
Pediatric Neurology , 10/20/09

Goldberg–Stern H et al. – This KCNQ2 mutation has implications for diagnosis and prognosis of familial neonatal seizures. Its presence suggests a benign disease with good prognosis and its identification can spare patients and physicians the need for extensive investigations or prolonged therapy.

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A 10-Month-Old Infant With Reversible Findings of Brain Death

Current and future treatment of epilepsy
The Internet Journal of Neurology, 11/03/09 Relevance Score: 91%

“It shouldn’t be something that's evil, it should be talked about”: A phenomenological approach to epilepsy and stigma
Seizure - European Journal of Epilepsy, 10/15/09 Relevance Score: 89%

Interictal EEG spikes identify the region of electrographic seizure onset in some, but not all, pediatric epilepsy patients
Epilepsia, 10/01/09 Relevance Score: 89%

Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy
Epilepsia, 10/01/09 Relevance Score: 89%

Pathologic cardiac repolarization in pharmacoresistant epilepsy and its potential role in sudden unexpected death in epilepsy: A case–control study
Epilepsia, 10/21/09 Relevance Score: 88%