Alice Bonuccelli

Efficacy and safety of continuous midazolam infusion in the treatment of acute repetitive seizures in non‐intensive settings: A multicenter retrospective real‐world data study

Alessandro Orsini, Lorenza Marini, Luca Bergonzini, Francesco D'Angelo et autres

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Phenotypic Spectrum in Individuals With Pathogenic Loss- and Gain-of-Function Variants

Alessandra Rossi, Susan X. N. Lin, Nathan L. Absalom, Sebastian Ortiz-De la Rosa et autres

Phenotypic Spectrum in Individuals With Pathogenic GABRG2 Loss- and Gain-of-Function Variants

Alessandra Rossi, Susan X. N. Lin, Nathan L. Absalom, Sebastian Ortiz-De la Rosa et autres

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Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience

Alessandro Orsini, Andrea Santangelo, Giorgio Costagliola, Massimo Scacciati et autres

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Hyperlysinemia, an ultrarare inborn error of metabolism: Review and update

Gemma Marinella, F Pascarella, Annalisa Vetro, Alice Bonuccelli et autres

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Exploring Headaches in Pediatric Behçet Disease: Prevalence, Clinical Impact, and Management

Andrea Santangelo, Antonio Corsello, Gilda Gizzi, Maddalena Lancieri et autres

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Infezione da West Nile Virus

Francesca Orsi, G. Bini, Giampiero I. Baroncelli, Alice Bonuccelli et autres

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An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review

Alessandro Orsini, Andrea Santangelo, Alessandra Carmignani, Anna Camporeale et autres

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Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay

Thomas Foiadelli, Andrea Santangelo, Giorgio Costagliola, Elisa Costa et autres

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Ataxia Telangiectasia Arising as Immunodeficiency: The Intriguing Differential Diagnosis

Federica Cavone, Susanna Cappelli, Alice Bonuccelli, Sofia D’Elios et autres

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Kabuki syndrome and rare tumors in a young girl carrying a frameshift kmt2d mutation

Alice Bonuccelli, Tommaso Baldaccini, Alessandro Orsini, Elisabetta Alberti et autres

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Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature

Gemma Marinella, Alessandro Orsini, Massimo Scacciati, Elisa Costa et autres

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