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Bone Marrow Transplantation|May 16, 2003
Mesial temporal sclerosis--a late complication in four allogeneic pediatric recipients with persistent seizures after an acute episode of cyclosporine-A neurotoxicityM Faraci, E Lanino, S Dallorso, et al.
Clinical and Experimental Obstetrics & Gynecology|May 11, 2018
Virtopsy in conjoined ischiopagus twinsM P Biso, P Sala, V G Vellone, et al.
Epilepsy Research|April 28, 2001
Distribution of epileptiform discharges during nREM sleep in the CSWSS syndrome: relationship with sigma and delta activitiesL Nobili, M G Baglietto, M Beelke, et al.
Clinical Genetics|July 18, 2002
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage diseaseR Biancheri, E Verbeek, A Rossi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 20, 2013
Anti-NMDAR encephalitis misdiagnosed as Hashimoto's encephalopathyM Mirabelli-Badenier, R Biancheri, G Morana, et al.
Neurology|December 25, 2002
Severe neurologic complications after hematopoietic stem cell transplantation in childrenM Faraci, E Lanino, G Dini, et al.
American Journal of Medical Genetics|April 1, 1992
Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infectionsE Bertini, R Cusmai, G de Saint Basile, et al.
Neurology|October 13, 2006
Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancyF Madia, P Striano, E Gennaro, et al.
Neurology|July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancyP Striano, A Coppola, M Pezzella, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
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