Volume 20, issue 4, August 2018

Review article

Genetic literacy series: genetic epilepsy with febrile seizures plus (p.232-8)
Kenneth A. Myers, Ingrid E. Scheffer, Samuel F. Berkovic
Free Access

Original articles

Identifying the educational needs of physicians in pediatric epilepsy in order to improve care: results from a needs assessment in Germany, Spain, and the United States (p.239-56)
Suzanne Murray, Sara Labbé, Sanjeev Kothare, Ignacio Málaga, Gerhard Kluger, Patti Ogden, Patrice Lazure, Alexis Arzimanoglou
Free Access

A comparison between the 1981 and 2017 International League Against Epilepsy classification of seizure types based on an outpatient setting (p.257-64)
Hui Gao, Josemir W. Sander, Yingfeng Xiao, Yingying Zhang, Dong Zhou
Free Access

Inadequate benzodiazepine dosing may result in progression to refractory and non-convulsive status epilepticus (p.265-9)
Shishir Keekana Rao, Advait Mahulikar, Mohammad Ibrahim, Aashit Shah, Navid Seraji-Bozorgzad, Wazim Mohamed
Free Access

Under-reporting of sudden unexpected death in epilepsy (p.270-8)
Sarah Chen, Golsa Joodi, Orrin Devinsky, Murrium I. Sadaf, Irion W. Pursell, Ross J. Simpson Jr
Free Access

Clinical commentaries

A child with hyperekplexia and epileptic myoclonus (p.279-82)
Lara Wadi, Yasser Medlej, Makram Obeid
Free Access

Epileptic ictal strabismus: a case report and review of the literature (p.283-8)
Francesco Brigo, Franco Alessandrini, Giammario Ragnedda, Piera Canu, Veronica Tavernelli, Arianna Bratti, Raffaele Nardone
Free Access

Neonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental andepileptic encephalopathy (p.289-94)
Linda Pons, Gaëtan Lesca, Damien Sanlaville, Nicolas Chatron, Audrey Labalme, Véronique Manel, Alexis Arzimanoglou, Julitta de Bellescize, Laurence Lion-François
Free Access

A triad of infantile spasms, nystagmus and a focal tonic seizure (p.295-300)
Stephanie Garcia Tarodo, Thu Nguyen, Emmanuelle Ranza, Serge Vulliémoz, Christian M. Korff
Free Access

Probable dysimmune epilepsia partialis continua manifesting as epileptic moving toes syndrome: electroclinical features of a challenging case (p.301-12)
Francesco Brigo, Alberto Vogrig, Arianna Bratti, Veronica Tavernelli, Raffaele Nardone, Eugen Trinka
Free Access

Biallelic loss-of-function UBA5 mutations in a patient with intractable West syndrome and profound failure to thrive (p.313-8)
Atsuro Daida, Shin-ichiro Hamano, Satoru Ikemoto, Ryuki Matsuura, Mitsuko Nakashima, Naomichi Matsumoto, Mitsuhiro Kato
Free Access