Rapid and safe response to low-dose carbamazepine in neonatal epilepsy

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

(2015) Bronwyn E. Grinton et al.   EPILEPSIA

Early and effective treatment ofKCNQ2encephalopathy

(2015) Tiziana Pisano et al.   EPILEPSIA

A novel KCNQ3 gene mutation in a child with infantile convulsions and partial epilepsy with centrotemporal spikes

(2015) Carlo Fusco et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

The phenotypic spectrum of SCN8A encephalopathy

(2015) J. Larsen et al.   NEUROLOGY

SCN2Aencephalopathy

(2015) Katherine B. Howell et al.   NEUROLOGY

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

(2015) Ragna S. Boerma et al.   Neurotherapeutics

Exacerbation of Benign Familial Neonatal Epilepsy Induced by Massive Doses of Phenobarbital and Midazolam

(2014) Tomoki Maeda et al.   PEDIATRIC NEUROLOGY

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

KCNQ2 encephalopathy: Delineation of the electroclinical phenotype and treatment response

(2013) A. L. Numis et al.   NEUROLOGY

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

PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine

(2012) C. Marini et al.   NEUROLOGY

Video-EEG monitoring in newborns with hypoxic-ischemic encephalopathy treated with hypothermia

(2011) K. B. Nash et al.   NEUROLOGY

Risk Factors for Epilepsy in Children With Neonatal Encephalopathy

(2011) Hannah C Glass et al.   PEDIATRIC RESEARCH

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

The Long-Term Effects of Neonatal Seizures

(2009) Gregory L. Holmes   CLINICS IN PERINATOLOGY

Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC)

(2009) Yoshihiro Sugiura et al.   EPILEPSY RESEARCH

Neutralization of a unique, negatively-charged residue in the voltage sensor of KV7.2 subunits in a sporadic case of benign familial neonatal seizures

(2009) Francesco Miceli et al.   NEUROBIOLOGY OF DISEASE

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures

(2009) H. Kurahashi et al.   NEUROLOGY

Altered KCNQ3 Potassium Channel Function Caused by the W309R Pore-Helix Mutation Found in Human Epilepsy

(2008) Akira Uehara et al.   JOURNAL OF MEMBRANE BIOLOGY

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes

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