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Genes|February 25, 2023
Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic ReviewLuca Bergonzini, Jacopo Pruccoli, Ilaria Pettenuzzo, et al.
Genes|July 2, 2021
Neurological Phenotype of Mowat-Wilson SyndromeDuccio Maria Cordelli, Veronica Di Pisa, Anna Fetta, et al.
Journal of Clinical Medicine|May 11, 2024
Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks ConsiderationAngelo Russo, Serena Mazzone, Laura Landolina, et al.
Children (Basel, Switzerland)|March 29, 2023
Post-Traumatic Headache in Children after Minor Head Trauma: Incidence, Phenotypes, and Risk FactorsArianna Dondi, Giovanni Battista Biserni, Sara Scarpini, et al.
Neuropediatrics|August 6, 2024
The Role of Electroencephalography in Children with Acute Altered Mental Status of Unknown Etiology: A Prospective StudyDaniela Chiarello, Annalisa Perrone, Emilia Ricci, et al.
The Journal of Pediatrics|July 29, 2023
Neurodevelopmental Correlates of Brain Magnetic Resonance Imaging Abnormalities in Extremely Low-birth-weight InfantsSilvia Martini, Jacopo Lenzi, Vittoria Paoletti, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|December 17, 2025
MOG IgG3-Subclass Antibodies in MOG-Associated Disease: Insights From a Pediatric Case With IgG1 Deficiency and Literature ReviewAnna Fetta, Francesca Conti, Agnese Lopalco, et al.
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