Search research articles
Contact Us
Filters
Showing results (211-220 of 260) with videos related to
Page
of 26
Sort By:
Epilepsy Research
|
May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients
Tiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Brain Sciences
|
November 27, 2021
Neuropsychological Sequelae, Quality of Life and Adaptive Behavior in Children and Adolescents with Anti-NMDAR Encephalitis: A Narrative Review
Samuela Tarantino, Roberto Averna, Claudia Ruscitto, et al.
Epilepsia Open
|
September 3, 2024
Epilepsy surgery below the age of 5 years: Are we still in time to preserve developmental and intellectual functions?
Simona Cappelletti, Cinzia Correale, Mattia Mercier, et al.
Pediatric Blood & Cancer
|
December 3, 2015
Metastatic Group 3 Medulloblastoma in a Patient With Tuberous Sclerosis Complex: Case Description and Molecular Characterization of the Tumor
Romina Moavero, Valentina Folgiero, Andrea Carai, et al.
Epilepsia
|
November 14, 2019
Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow-up
Nicola Specchio, Nicola Pietrafusa, Marcello Bellusci, et al.
Neonatology
|
February 27, 2022
Neonatal Cerebral Venous Thrombosis following Maternal SARS-CoV-2 Infection in Pregnancy
Francesca Campi, Daniela Longo, Iliana Bersani, et al.
Epilepsia
|
September 18, 2020
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study
Nicola Specchio, Nicola Pietrafusa, Viola Doccini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 24, 2016
Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia
Lorena Travaglini, Marta Nardella, Emanuele Bellacchio, et al.
Brain Sciences
|
July 2, 2021
The Role of KRAS Mutations in Cortical Malformation and Epilepsy Surgery: A Novel Report of Nevus Sebaceous Syndrome and Review of the Literature
Chiara Pepi, Luca de Palma, Marina Trivisano, et al.
Epilepsia
|
January 13, 2023
Gain of function SCN1A disease-causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication
Sara Matricardi, Sandrine Cestèle, Marina Trivisano, et al.
Page
of 26
Search research articles
Search
Showing results (211-220 of 260) with videos related to
Sort By:
Page
of 26
Epilepsy Research
|
May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients
Tiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Brain Sciences
|
November 27, 2021
Neuropsychological Sequelae, Quality of Life and Adaptive Behavior in Children and Adolescents with Anti-NMDAR Encephalitis: A Narrative Review
Samuela Tarantino, Roberto Averna, Claudia Ruscitto, et al.
Epilepsia Open
|
September 3, 2024
Epilepsy surgery below the age of 5 years: Are we still in time to preserve developmental and intellectual functions?
Simona Cappelletti, Cinzia Correale, Mattia Mercier, et al.
Pediatric Blood & Cancer
|
December 3, 2015
Metastatic Group 3 Medulloblastoma in a Patient With Tuberous Sclerosis Complex: Case Description and Molecular Characterization of the Tumor
Romina Moavero, Valentina Folgiero, Andrea Carai, et al.
Epilepsia
|
November 14, 2019
Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow-up
Nicola Specchio, Nicola Pietrafusa, Marcello Bellusci, et al.
Neonatology
|
February 27, 2022
Neonatal Cerebral Venous Thrombosis following Maternal SARS-CoV-2 Infection in Pregnancy
Francesca Campi, Daniela Longo, Iliana Bersani, et al.
Epilepsia
|
September 18, 2020
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study
Nicola Specchio, Nicola Pietrafusa, Viola Doccini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 24, 2016
Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia
Lorena Travaglini, Marta Nardella, Emanuele Bellacchio, et al.
Brain Sciences
|
July 2, 2021
The Role of KRAS Mutations in Cortical Malformation and Epilepsy Surgery: A Novel Report of Nevus Sebaceous Syndrome and Review of the Literature
Chiara Pepi, Luca de Palma, Marina Trivisano, et al.
Epilepsia
|
January 13, 2023
Gain of function SCN1A disease-causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication
Sara Matricardi, Sandrine Cestèle, Marina Trivisano, et al.
Page
of 26