Search research articles
Contact Us
Filters
Showing results (1-10 of 87) with videos related to
Page
of 9
Sort By:
Epilepsia
|
April 6, 2011
Cognitive development in children with Dravet syndrome
Francesca Ragona
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 3, 2018
ATP1A3-related disorders: An update
Miryam Carecchio, Giovanna Zorzi, Francesca Ragona, et al.
Neuropediatrics
|
June 4, 2014
Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review
Francesca Ragona, Sara Matricardi, Barbara Castellotti, et al.
Epilepsy & Behavior : E&B
|
January 17, 2016
Neuropsychological profiles and outcomes in children with new onset frontal lobe epilepsy
Sara Matricardi, Francesco Deleo, Francesca Ragona, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 4, 2018
Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders
Tiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Journal of Neuroimmunology
|
November 30, 2002
Antibodies against GluR3 peptides are not specific for Rasmussen's encephalitis but are also present in epilepsy patients with severe, early onset disease and intractable seizures
Renato Mantegazza, Pia Bernasconi, Fulvio Baggi, et al.
Journal of Neurology
|
February 18, 2016
Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis
Sara Matricardi, Mara Patrini, Elena Freri, et al.
Expert Opinion on Pharmacotherapy
|
April 6, 2023
Cannabidiol use in patients with Dravet syndrome and Lennox-Gastaut syndrome: experts' opinions using a nominal group technique (NGT) approach
Paolo Bonanni, Francesca Ragona, Carlo Fusco, et al.
Journal of Child Neurology
|
October 31, 2013
A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern
Romina Romaniello, Claudio Zucca, Erika Tenderini, et al.
Developmental Medicine and Child Neurology
|
June 9, 2019
Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis
Margherita Nosadini, Tiziana Granata, Sara Matricardi, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 87) with videos related to
Sort By:
Page
of 9
Epilepsia
|
April 6, 2011
Cognitive development in children with Dravet syndrome
Francesca Ragona
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 3, 2018
ATP1A3-related disorders: An update
Miryam Carecchio, Giovanna Zorzi, Francesca Ragona, et al.
Neuropediatrics
|
June 4, 2014
Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review
Francesca Ragona, Sara Matricardi, Barbara Castellotti, et al.
Epilepsy & Behavior : E&B
|
January 17, 2016
Neuropsychological profiles and outcomes in children with new onset frontal lobe epilepsy
Sara Matricardi, Francesco Deleo, Francesca Ragona, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 4, 2018
Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders
Tiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Journal of Neuroimmunology
|
November 30, 2002
Antibodies against GluR3 peptides are not specific for Rasmussen's encephalitis but are also present in epilepsy patients with severe, early onset disease and intractable seizures
Renato Mantegazza, Pia Bernasconi, Fulvio Baggi, et al.
Journal of Neurology
|
February 18, 2016
Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis
Sara Matricardi, Mara Patrini, Elena Freri, et al.
Expert Opinion on Pharmacotherapy
|
April 6, 2023
Cannabidiol use in patients with Dravet syndrome and Lennox-Gastaut syndrome: experts' opinions using a nominal group technique (NGT) approach
Paolo Bonanni, Francesca Ragona, Carlo Fusco, et al.
Journal of Child Neurology
|
October 31, 2013
A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern
Romina Romaniello, Claudio Zucca, Erika Tenderini, et al.
Developmental Medicine and Child Neurology
|
June 9, 2019
Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis
Margherita Nosadini, Tiziana Granata, Sara Matricardi, et al.
Page
of 9