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Nelia Zamponi

Showing results (31-40 of 50) with videos related to

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Journal of Child Neurology|April 13, 2011
Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of lifeStefano Sartori, Roberta Polli, Elisa Bettella, et al.
Epilepsia|April 24, 2014
The long-term effect of vagus nerve stimulation on quality of life in patients with pharmacoresistant focal epilepsy: the PuLsE (Open Prospective Randomized Long-term Effectiveness) trialPhilippe Ryvlin, Frank G Gilliam, Dang K Nguyen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2022
Knowledge and attitudes of neurologists toward epilepsy surgery: an Italian surveySara Casciato, Alessandra Morano, Lorenzo Ricci, et al.
World Neurosurgery|October 12, 2018
CD34 Expression in Low-Grade Epilepsy-Associated Tumors: Relationships with Clinicopathologic FeaturesMarco Giulioni, Gianluca Marucci, Massimo Cossu, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
The Journal of Pediatrics|September 3, 2013
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndromeAlberto Verrotti, Raffaella Cusmai, Francesco Nicita, et al.
Epilepsy Research|December 15, 2010
Benign convulsions associated with mild gastroenteritis: a multicenter clinical studyAlberto Verrotti, Giuliana Nanni, Sergio Agostinelli, et al.
Seizure|January 10, 2013
Lacosamide in pediatric and adult patients: comparison of efficacy and safetyAlberto Verrotti, Giulia Loiacono, Antonella Pizzolorusso, et al.
Plos One|October 30, 2014
PDCD10 gene mutations in multiple cerebral cavernous malformationsMaria Sole Cigoli, Francesca Avemaria, Stefano De Benedetti, et al.
Epilepsia|September 6, 2012
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsyCarla Marini, Francesca Darra, Nicola Specchio, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Journal of Child Neurology|April 13, 2011
Pathogenic role of the X-linked cyclin-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of lifeStefano Sartori, Roberta Polli, Elisa Bettella, et al.
Epilepsia|April 24, 2014
The long-term effect of vagus nerve stimulation on quality of life in patients with pharmacoresistant focal epilepsy: the PuLsE (Open Prospective Randomized Long-term Effectiveness) trialPhilippe Ryvlin, Frank G Gilliam, Dang K Nguyen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 21, 2022
Knowledge and attitudes of neurologists toward epilepsy surgery: an Italian surveySara Casciato, Alessandra Morano, Lorenzo Ricci, et al.
World Neurosurgery|October 12, 2018
CD34 Expression in Low-Grade Epilepsy-Associated Tumors: Relationships with Clinicopathologic FeaturesMarco Giulioni, Gianluca Marucci, Massimo Cossu, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
The Journal of Pediatrics|September 3, 2013
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndromeAlberto Verrotti, Raffaella Cusmai, Francesco Nicita, et al.
Epilepsy Research|December 15, 2010
Benign convulsions associated with mild gastroenteritis: a multicenter clinical studyAlberto Verrotti, Giuliana Nanni, Sergio Agostinelli, et al.
Seizure|January 10, 2013
Lacosamide in pediatric and adult patients: comparison of efficacy and safetyAlberto Verrotti, Giulia Loiacono, Antonella Pizzolorusso, et al.
Plos One|October 30, 2014
PDCD10 gene mutations in multiple cerebral cavernous malformationsMaria Sole Cigoli, Francesca Avemaria, Stefano De Benedetti, et al.
Epilepsia|September 6, 2012
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsyCarla Marini, Francesca Darra, Nicola Specchio, et al.
Pageof 5