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Alberto Verrottı

Observed names: A Verrotti, A. Verrotti, ALBERTO VERROTTI, Alberto VERROTTI, Alberto Verrotti, Verrotti, A
Observed institutions: Medical University of South Carolina, University of Pavia, University of L'Aquila, University of Perugia, Azienda Ospedaliera di Perugia, San Salvatore Hospital, National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, University College London
ORCID: 0000-0001-6323-4187
Observed ORCIDs: 0000-0001-6323-4187, 0009-0001-2403-1990
OpenAlex ID: A5101624533
The Pharmacoresistant Epilepsy: An Overview on Existent and New Emerging Therapies
2021 · Antonella Fattorusso, Sara Matricardi, et al. · Frontiers in Neurology · 269
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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
2019 · Vincenzo Salpietro, Christine L. Dixon, et al. · Nature Communications · 250
Microbiota-gut brain axis involvement in neuropsychiatric disorders
2019 · Luigi Francesco Iannone, Alberto Preda, et al. · Expert Review of Neurotherapeutics · 177
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Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
2020 · Lucia V. Schottlaender, Rosella Abeti, et al. · The American Journal of Human Genetics · 88
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The pharmacological management of Lennox-Gastaut syndrome and critical literature review
2018 · Alberto Verrotti, Pasquale Striano, et al. · Seizure · 79
Efficacy of ketogenic diet for infantile spasms: A systematic review
2017 · G. Prezioso, G. Carlone, et al. · Acta Neurologica Scandinavica · 79
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Diet in the Treatment of Epilepsy: What We Know So Far
2020 · Alberto Verrotti, Giulia Iapadre, et al. · Nutrients · 75
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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
2019 · Stephanie Efthymiou, Vincenzo Salpietro, et al. · Brain · 71
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Using the Social Robot NAO for Emotional Support to Children at a Pediatric Emergency Department: Randomized Clinical Trial
2021 · Silvia Rossi, Silvano Junior Santini, et al. · Journal of Medical Internet Research · 51
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants
2020 · Caroline Neuray, Reza Maroofian, et al. · Brain · 50
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Child Abuse and Neglect and its Psycho-Physical and Social Consequences: A Review of the Literature
2016 · P. Ferrara, C. Guadagno, et al. · Current Pediatric Reviews · 49
Perampanel tolerability in children and adolescents with focal epilepsy: Effects on behavior and executive functions
2020 · Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, et al. · Epilepsy & Behavior · 46
Children with developmental dyslexia showed greater sleep disturbances than controls, including problems initiating and maintaining sleep
2016 · M Carotenuto, M Esposito, et al. · Acta Paediatrica · 46
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The Ketogenic Diet for the Treatment of Mood Disorders in Comorbidity With Epilepsy in Children and Adolescents
2020 · Francesca Felicia Operto, Sara Matricardi, et al. · Frontiers in Pharmacology · 45
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Melkersson–Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature
2019 · Salvatore Savasta, Alessandra Rossi, et al. · International Journal of Environmental Research and Public Health · 45
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Pharmacokinetics and Drug Interaction of Antiepileptic Drugs in Children and Adolescents
2018 · Giulia Iapadre, Ganna Balagura, et al. · Pediatric Drugs · 43
Femicide and murdered women’s children: which future for these children orphans of a living parent?
2015 · Pietro Ferrara, Olga Caporale, et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 41
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Fenfluramine for the Treatment of Dravet Syndrome and Lennox–Gastaut Syndrome
2020 · Ganna Balagura, Marta Cacciatore, et al. · CNS Drugs · 39
Social cognition and executive functions in children and adolescents with focal epilepsy
2020 · Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, et al. · European Journal of Paediatric Neurology · 37
Clitoromegaly in Childhood and Adolescence: Behind One Clinical Sign, a Clinical Sea
2018 · Maria L. Iezzi, Stefania Lasorella, et al. · Sexual Development · 36
Epilepsy is a possible feature in Williams‐Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region
2015 · Francesco Nicita, Giacomo Garone, et al. · American Journal of Medical Genetics Part A · 35
Effects on executive functions of antiepileptic monotherapy in pediatric age
2019 · Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, et al. · Epilepsy & Behavior · 33
Cognitive profile in BECTS treated with levetiracetam: A 2-year follow-up
2019 · Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, et al. · Epilepsy & Behavior · 33
Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review
2017 · M. Greco, P. Ferrara, et al. · Epilepsy Research · 28
72nd Congress of the Italian Society of Pediatrics
2017 · Marco Braghero, Annamaria Staiano, et al. · ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics · 28
Works count: 85
Citation count: 2,373
H-index: 26
I10-index: 54
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