Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

(2013) Federico Zara et al.   EPILEPSIA

NovelKCNQ2andKCNQ3Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin-1A

(2013) Maria Virginia Soldovieri et al.   HUMAN MUTATION

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

(2012) Sarah E. Heron et al.   AMERICAN JOURNAL OF HUMAN GENETICS

KCNQ2 abnormality in BECTS: Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2

(2012) Atsushi Ishii et al.   EPILEPSY RESEARCH

An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy

(2011) Gerald Raymond et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

(2011) Sarah Weckhuysen et al.   ANNALS OF NEUROLOGY

Proposed genetic classification of the “benign” familial neonatal and infantile epilepsies

(2011) John C. Mulley et al.   EPILEPSIA

Refractory neonatal epilepsy with a de novo duplication of chromosome 2q24.2q24.3

(2011) Akihisa Okumura et al.   EPILEPSIA

Metabolic and monogenic causes of seizures in neonates and young infants

(2011) Johan L.K. Van Hove et al.   MOLECULAR GENETICS AND METABOLISM

Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3

(2010) Sarah E. Heron et al.   EPILEPSIA

The First Korean Case of KCNQ2 Mutation in a Family with Benign Familial Neonatal Convulsions

(2010) Mi-Sun Yum et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

Novel Mutation in KCNQ2 Causing Benign Familial Neonatal Seizures

(2009) Hadassa Goldberg-Stern et al.   PEDIATRIC NEUROLOGY

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes

(2008) B. A. Neubauer et al.   NEUROLOGY