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Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Epilepsia|March 1, 1997
Early-onset benign occipital seizure susceptibility syndromeC D Ferrie, A Beaumanoir, R Guerrini, et al.
Clinical Genetics|April 27, 2011
Fabry disease: polymorphic haplotypes and a novel missense mutation in the GLA geneL Ferri, C Guido, G la Marca, et al.
Journal of the Neurological Sciences|June 4, 2021
Seizure outcome after epilepsy surgery in tuberous sclerosis complex: Results and analysis of predictors from a multicenter studyC Vannicola, L Tassi, C Barba, et al.
Epilepsia|October 3, 2001
Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate resultsA Bernasconi, V Martinez, P Rosa-Neto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 24, 2024
Home-based, computer-assisted cognitive rehabilitation for attention in pediatric onset multiple sclerosis: a randomized, multicenter pilot studyCamilla Masciulli, E Portaccio, B Goretti, et al.
Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, et al.
Brain : a Journal of Neurology|May 11, 2006
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutationsE Parrini, A Ramazzotti, W B Dobyns, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2015
Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsyA Müller, I Helbig, C Jansen, et al.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
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