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Massimo Mastrangelo

Showing results (41-50 of 58) with videos related to

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International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 20, 2011
Definition of the neurological phenotype associated with dup (X)(p11.22-p11.23)Marcella Broli, Francesca Bisulli, Massimo Mastrangelo, 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.
Neurology|March 31, 2026
Genetic Etiologies of Epilepsies With Status Epilepticus: Insights From the Italian Pediatric Status Epilepticus Group CohortCarla Marini, Anna Rosati, Lucia Fusco, et al.
Pediatric Research|May 20, 2026
Electrographic-only seizures and status epilepticus in neonates with Tuberous Sclerosis ComplexSerena Pellegrin, Massimo Mastrangelo, Patrizia Accorsi, et al.
Epilepsia Open|July 14, 2022
KETASER01 protocol: What went right and what went wrongAnna Rosati, Manuela L'Erario, Roberto Bianchi, et al.
BMJ Open|June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Epilepsia|May 16, 2025
Optimizing pediatric status epilepticus management: The role of early midazolam infusion and adherence to clinical practice guidelinesAnna Rosati, Patrizia Bartolotta, Carla Marini, et al.
American Journal of Human Genetics|September 1, 2009
Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and femalesRoberto Giorda, M Clara Bonaglia, Silvana Beri, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 20, 2011
Definition of the neurological phenotype associated with dup (X)(p11.22-p11.23)Marcella Broli, Francesca Bisulli, Massimo Mastrangelo, 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.
Neurology|March 31, 2026
Genetic Etiologies of Epilepsies With Status Epilepticus: Insights From the Italian Pediatric Status Epilepticus Group CohortCarla Marini, Anna Rosati, Lucia Fusco, et al.
Pediatric Research|May 20, 2026
Electrographic-only seizures and status epilepticus in neonates with Tuberous Sclerosis ComplexSerena Pellegrin, Massimo Mastrangelo, Patrizia Accorsi, et al.
Epilepsia Open|July 14, 2022
KETASER01 protocol: What went right and what went wrongAnna Rosati, Manuela L'Erario, Roberto Bianchi, et al.
BMJ Open|June 18, 2016
Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01)Anna Rosati, Lucrezia Ilvento, Manuela L'Erario, et al.
Epilepsia|January 31, 2013
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significanceFederico Zara, Nicola Specchio, Pasquale Striano, et al.
Epilepsia|May 16, 2025
Optimizing pediatric status epilepticus management: The role of early midazolam infusion and adherence to clinical practice guidelinesAnna Rosati, Patrizia Bartolotta, Carla Marini, et al.
American Journal of Human Genetics|September 1, 2009
Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and femalesRoberto Giorda, M Clara Bonaglia, Silvana Beri, et al.
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