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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2020
Is Covid-19 lockdown related to an increase of accesses for seizures in the emergency department? An observational analysis of a paediatric cohort in the Southern ItalyFederica Palladino, Eugenio Merolla, Marella Solimeno, et al.Epilepsia|May 13, 2014
Seizures in fetal alcohol spectrum disorders: evaluation of clinical, electroencephalographic, and neuroradiologic features in a pediatric case seriesFrancesco Nicita, Alberto Verrotti, Dario Pruna, et al.Neuropharmacology|September 7, 2021
Increased efficacy of combining prebiotic and postbiotic in mouse models relevant to autism and depressionAntonio Leo, Carmen De Caro, Paolo Mainardi, et al.Neurogenetics|January 31, 2008
Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian familiesFrancesca Madia, Pasquale Striano, Carlo Di Bonaventura, et al.Expert Review of Neurotherapeutics|February 4, 2021
Managing CLN2 disease: a treatable neurodegenerative condition among other treatable early childhood epilepsiesMaria Mazurkiewicz-Bełdzińska, Mireia Del Toro, Göknur Haliloğlu, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2018
Spinal motor neuron involvement in a patient with homozygous PRUNE mutationMichele Iacomino, Chiara Fiorillo, Annalaura Torella, et al.Epilepsia|June 16, 2010
Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug-refractory epilepsyMaria Paola Canevini, Giovambattista De Sarro, Carlo Andrea Galimberti, et al.Neurology. Genetics|May 27, 2016
White matter involvement in a family with a novel PDGFB mutationRoberta Biancheri, Mariasavina Severino, Angela Robbiano, et al.Epilepsia|February 4, 2009
Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patientsEdoardo Ferlazzo, Constant K Adjien, Renzo Guerrini, et al.Journal of Epilepsy Research|March 4, 2021
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language ImpairmentPiero Pavone, Xena Giada Pappalardo, Ugochi Ngaobiri Nelly Ohazuruike, et al.Pageof 68