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P Striano

Showing results (41-50 of 57) with videos related to

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Brain : a Journal of Neurology|April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic casesF Bisulli, P Tinuper, P Avoni, et al.
Neurology|April 13, 2012
LGI1 microdeletion in autosomal dominant lateral temporal epilepsyM Fanciulli, L Santulli, L Errichiello, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Journal of Psychiatric Research|January 28, 2021
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreakA Orsini, M Corsi, V Pedrinelli, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, 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.
Acta Neurologica Scandinavica|January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)S Matricardi, F Darra, A Spalice, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 1, 2019
Clinical and genetic spectrum of SCN2A-associated episodic ataxiaN Schwarz, T Bast, E Gaily, et al.
Epilepsy Research|May 19, 2006
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsyA Ayerdi-Izquierdo, G Stavrides, J J Sellés-Martínez, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Brain : a Journal of Neurology|April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic casesF Bisulli, P Tinuper, P Avoni, et al.
Neurology|April 13, 2012
LGI1 microdeletion in autosomal dominant lateral temporal epilepsyM Fanciulli, L Santulli, L Errichiello, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Journal of Psychiatric Research|January 28, 2021
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreakA Orsini, M Corsi, V Pedrinelli, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, 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.
Acta Neurologica Scandinavica|January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)S Matricardi, F Darra, A Spalice, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 1, 2019
Clinical and genetic spectrum of SCN2A-associated episodic ataxiaN Schwarz, T Bast, E Gaily, et al.
Epilepsy Research|May 19, 2006
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsyA Ayerdi-Izquierdo, G Stavrides, J J Sellés-Martínez, et al.
Pageof 6