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Brain : a Journal of Neurology|May 29, 2000
Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European familiesF Picard, S Baulac, P Kahane, et al.Neurology|June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformationM D D'Agostino, A Bastos, C Piras, et al.Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2002
Intravenous immunoglobulin in neurological disease: a specialist reviewC M Wiles, P Brown, H Chapel, et al.Neurology|January 13, 2012
FLNA genomic rearrangements cause periventricular nodular heterotopiaK R Clapham, T W Yu, V S Ganesh, et al.Nature Communications|August 2, 2014
Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine modelN Lozovaya, S Gataullina, T Tsintsadze, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panelL Vignatelli, E Antelmi, I Ceretelli, et al.Epilepsia|June 1, 2001
The costs of childhood epilepsy in Italy: comparative findings from three health care settingsR Guerrini, R Battini, A R Ferrari, et al.Neurology|December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionC Cardoso, A Boys, E Parrini, et al.Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.Pageof 45