epilepsy

Co-occurring malformations of cortical development and SCN1A gene mutations.

Barba C, Parrini E, Coras R, Galuppi A, Craiu D, Kluger G, et al. Co-occurring malformations of cortical development and SCN1A gene mutations. Epilepsia. 2014;55(7):1009-19. DOI: 10.1111/epi.12658. PubMed PMID: 24902755.

Sofie's journey.

Levy C, Levy B. Sofie's journey. Epilepsia. 2014;55(9):1329-30. DOI: 10.1111/epi.12664. PubMed PMID: 24903458.

Seizure frequency and patient-centered outcome assessment in epilepsy.

Choi H, Hamberger MJ, Munger Clary H, Loeb R, Onchiri FM, Baker G, et al. Seizure frequency and patient-centered outcome assessment in epilepsy. Epilepsia. 2014;55(8):1205-12. DOI: 10.1111/epi.12672. PubMed PMID: 24903898.

Automated detection of cortical dysplasia type II in MRI-negative epilepsy.

Hong S-J, Kim H, Schrader D, Bernasconi N, Bernhardt BC, Bernasconi A. Automated detection of cortical dysplasia type II in MRI-negative epilepsy. Neurology. 2014;83(1):48-55. DOI: 10.1212/WNL.0000000000000543. PubMed PMID: 24898923.

Interrater agreement for Critical Care EEG Terminology.

Gaspard N, Hirsch LJ, Laroche SM, Hahn CD, Westover MB. Interrater agreement for Critical Care EEG Terminology. Epilepsia. 2014;55(9):1366-73. DOI: 10.1111/epi.12653. PubMed PMID: 24888711.

Early onset epileptic encephalopathy caused by de novo SCN8A mutations.

Ohba C, Kato M, Takahashi S, Lerman-Sagie T, Lev D, Terashima H, et al. Early onset epileptic encephalopathy caused by de novo SCN8A mutations. Epilepsia. 2014;55(7):994-1000. DOI: 10.1111/epi.12668. PubMed PMID: 24888894.

Author response.

Lamberts RJ, Gaitatzis A, Sander JW, Elger CE, Surges R, Thijs RD. Author response. Neurology. 2014;82(16):1480. PubMed PMID: 24877220.