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Alessandro Orsini

Showing results (51-60 of 110) with videos related to

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Frontiers in Neurology|April 1, 2022
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical ApplicationsGiorgio Costagliola, Greta Depietri, Alexandre Michev, et al.
Genes|April 27, 2024
An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature ReviewAlessandro Orsini, Andrea Santangelo, Alessandra Carmignani, et al.
Genes|July 29, 2023
Congenital Myopathy as a Phenotypic Expression of <i>CACNA1S</i> Gene Mutation: Case Report and Systematic Review of the LiteratureGemma Marinella, Alessandro Orsini, Massimo Scacciati, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 18, 2024
IL-17 in serum and cerebrospinal fluid of pediatric patients with acute neuropsychiatric disorders: Implications for PANDAS and PANSThomas Foiadelli, Nicolò Loddo, Lucia Sacchi, et al.
Epilepsy & Behavior : E&B|February 26, 2022
De novo GRIN2A variants associated with epilepsy and autism and literature reviewGiuseppe Donato Mangano, Antonella Riva, Antonina Fontana, et al.
Frontiers in Neurology|August 28, 2023
Pediatric hypnic headache: a systematic reviewAlessandro Ferretti, Margherita Velardi, Claudia Fanfoni, et al.
Children (Basel, Switzerland)|June 28, 2023
Digital Devices Use and Fine Motor Skills in Children between 3-6 YearsFrancesca Felicia Operto, Andrea Viggiano, Antonio Perfetto, et al.
Acta Bio-Medica : Atenei Parmensis|April 20, 2022
Peripheral Arterial Tonometry (EndoPAT)-measured Endothelial Dysfunction in Migraine with Aura childrenAlice Bonuccelli, Claudia Sciarrotta, Maria Grazia Esposito, et al.
Neurology. Genetics|August 18, 2017
Novel <i>AMPD2</i> mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalitiesAndrea Accogli, Michele Iacomino, Francesca Pinto, et al.
Journal of Clinical Medicine|October 16, 2025
Advancing Non-Invasive Ophthalmic Imaging in Sturge-Weber Syndrome: Clinical Guidelines Towards Early Choroidal Hemangioma DetectionMariachiara Di Pippo, Daria Rullo, Chiara Ciancimino, et al.
Pageof 11

Showing results (51-60 of 110) with videos related to

Sort By:
Pageof 11
Frontiers in Neurology|April 1, 2022
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical ApplicationsGiorgio Costagliola, Greta Depietri, Alexandre Michev, et al.
Genes|April 27, 2024
An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature ReviewAlessandro Orsini, Andrea Santangelo, Alessandra Carmignani, et al.
Genes|July 29, 2023
Congenital Myopathy as a Phenotypic Expression of <i>CACNA1S</i> Gene Mutation: Case Report and Systematic Review of the LiteratureGemma Marinella, Alessandro Orsini, Massimo Scacciati, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 18, 2024
IL-17 in serum and cerebrospinal fluid of pediatric patients with acute neuropsychiatric disorders: Implications for PANDAS and PANSThomas Foiadelli, Nicolò Loddo, Lucia Sacchi, et al.
Epilepsy & Behavior : E&B|February 26, 2022
De novo GRIN2A variants associated with epilepsy and autism and literature reviewGiuseppe Donato Mangano, Antonella Riva, Antonina Fontana, et al.
Frontiers in Neurology|August 28, 2023
Pediatric hypnic headache: a systematic reviewAlessandro Ferretti, Margherita Velardi, Claudia Fanfoni, et al.
Children (Basel, Switzerland)|June 28, 2023
Digital Devices Use and Fine Motor Skills in Children between 3-6 YearsFrancesca Felicia Operto, Andrea Viggiano, Antonio Perfetto, et al.
Acta Bio-Medica : Atenei Parmensis|April 20, 2022
Peripheral Arterial Tonometry (EndoPAT)-measured Endothelial Dysfunction in Migraine with Aura childrenAlice Bonuccelli, Claudia Sciarrotta, Maria Grazia Esposito, et al.
Neurology. Genetics|August 18, 2017
Novel <i>AMPD2</i> mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalitiesAndrea Accogli, Michele Iacomino, Francesca Pinto, et al.
Journal of Clinical Medicine|October 16, 2025
Advancing Non-Invasive Ophthalmic Imaging in Sturge-Weber Syndrome: Clinical Guidelines Towards Early Choroidal Hemangioma DetectionMariachiara Di Pippo, Daria Rullo, Chiara Ciancimino, et al.
Pageof 11