Latest papers

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

Gaussian process modeling of EEG for the detection of neonatal seizures.

A multistage knowledge-based system for EEG seizure detection in newborn infants.

Mutation analysis of WASF2 and GALE genes in one Chinese family with benign familial infantile convulsions with a novel locus.

Treatment of pediatric epilepsy: European expert opinion, 2007.

Prognosis of neonatal seizures: It's the etiology, Stupid--or is it?

K+ M-current regulates the transition to seizures in immature and adult hippocampus.

SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.

Focal motor seizure with automatisms in a newborn.

Proposal of an algorithm for diagnosis and treatment of neonatal seizures in developing countries.

[The effect of neonatal convulsions and antiepileptic drugs on the developing brain: controversial aspects and therapeutic implications].

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

Seizure recurrence and developmental disabilities after neonatal seizures: outcomes are unrelated to use of phenobarbital prophylaxis.

Benign familial neonatal convulsions: always benign?

Neonatal convulsions secondary to paroxetine withdrawal.

A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC).

Neonatal seizures: gaps between the laboratory and the clinic.

Correlating the clinical and genetic features of benign familial neonatal seizures (BFNS) with the functional consequences of underlying mutations.

Ictal EEG in patients with convulsions with mild gastroenteritis.

Benign Myoclonic Epilepsy in Infancy (BMEI): A Longitudinal Electroclinical Study of 22 Cases