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Massimo Mastrangelo

Showing results (11-20 of 58) with videos related to

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Hormone Research in Paediatrics|September 13, 2017
Short-Term Vitamin D3 Supplementation in Children with Neurodisabilities: Comparison of Two Delivery MethodsFrancesca Penagini, Barbara Borsani, Katia Maruca, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 28, 2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathyMassimo Mastrangelo, Angela Peron, Luigina Spaccini, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 12, 2005
The Milan Project: a newborn hearing screening programmeGiancarlo Pastorino, Paola Sergi, Massimo Mastrangelo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 31, 2012
Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR)Elena Antelmi, Massimo Mastrangelo, Francesca Bisulli, et al.
Brain Sciences|July 2, 2021
Reply to Dravet, C. Different Outcomes of Acute Encephalopathy after Status Epilepticus in Patients with Dravet Syndrome. How to Avoid Them? Comment on "De Liso et al. Fatal Status Epilepticus in Dravet Syndrome. <i>Brain Sci</i>. 2020, <i>10</i>, 889"Paola De Liso, Virginia Pironi, Massimo Mastrangelo, et al.
Brain Sciences|November 26, 2020
Fatal Status Epilepticus in Dravet SyndromePaola De Liso, Virginia Pironi, Massimo Mastrangelo, et al.
JACC. Case Reports|September 17, 2025
Amplitude-Integrated/Continuous Electroencephalography for Early Detection of Low Cardiac Output After Chest Closure in an InfantAlessandro Barbaria, Mariarita Capizzi, Federica Sperandeo, et al.
American Journal of Medical Genetics. Part A|July 31, 2013
Snyder-Robinson syndrome: a novel nonsense mutation in spermine synthase and expansion of the phenotypeAngela Peron, Luigina Spaccini, Joy Norris, et al.
Journal of Child Neurology|January 10, 2008
High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemiaMassimo Mastrangelo, Laura Canafoglia, Silvana Franceschetti, et al.
Epilepsy & Behavior : E&B|November 26, 2019
Management of status epilepticus in adults. Position paper of the Italian League against EpilepsyFabio Minicucci, Monica Ferlisi, Francesco Brigo, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Hormone Research in Paediatrics|September 13, 2017
Short-Term Vitamin D3 Supplementation in Children with Neurodisabilities: Comparison of Two Delivery MethodsFrancesca Penagini, Barbara Borsani, Katia Maruca, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 28, 2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathyMassimo Mastrangelo, Angela Peron, Luigina Spaccini, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 12, 2005
The Milan Project: a newborn hearing screening programmeGiancarlo Pastorino, Paola Sergi, Massimo Mastrangelo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 31, 2012
Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR)Elena Antelmi, Massimo Mastrangelo, Francesca Bisulli, et al.
Brain Sciences|July 2, 2021
Reply to Dravet, C. Different Outcomes of Acute Encephalopathy after Status Epilepticus in Patients with Dravet Syndrome. How to Avoid Them? Comment on "De Liso et al. Fatal Status Epilepticus in Dravet Syndrome. <i>Brain Sci</i>. 2020, <i>10</i>, 889"Paola De Liso, Virginia Pironi, Massimo Mastrangelo, et al.
Brain Sciences|November 26, 2020
Fatal Status Epilepticus in Dravet SyndromePaola De Liso, Virginia Pironi, Massimo Mastrangelo, et al.
JACC. Case Reports|September 17, 2025
Amplitude-Integrated/Continuous Electroencephalography for Early Detection of Low Cardiac Output After Chest Closure in an InfantAlessandro Barbaria, Mariarita Capizzi, Federica Sperandeo, et al.
American Journal of Medical Genetics. Part A|July 31, 2013
Snyder-Robinson syndrome: a novel nonsense mutation in spermine synthase and expansion of the phenotypeAngela Peron, Luigina Spaccini, Joy Norris, et al.
Journal of Child Neurology|January 10, 2008
High-frequency rhythmic cortical myoclonus in a long-surviving patient with nonketotic hypergylcemiaMassimo Mastrangelo, Laura Canafoglia, Silvana Franceschetti, et al.
Epilepsy & Behavior : E&B|November 26, 2019
Management of status epilepticus in adults. Position paper of the Italian League against EpilepsyFabio Minicucci, Monica Ferlisi, Francesco Brigo, et al.
Pageof 6