Get started
Author

Antonio Varone

Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
2022 · Margherita Nosadini, Michael Eyre, et al. · Neurology Neuroimmunology & Neuroinflammation · 80
PDF
Onasemnogene abeparvovec gene replacement therapy for the treatment of spinal muscular atrophy: a real-world observational study
2022 · Ilaria Bitetti, Valentina Lanzara, et al. · Gene Therapy · 64
PDF
Pseudotumor cerebri
2010 · Pietro Spennato, Claudio Ruggiero, et al. · Child s Nervous System · 58
Neuroendoscopic management of interhemispheric cysts in children
2006 · Giuseppe Cinalli, Paola Peretta, et al. · Journal of Neurosurgery Pediatrics · 55
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey
2022 · Giorgia Coratti, Martina Ricci, et al. · Neurology · 51
PDF
Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapies
2023 · Marika Pane, Beatrice Berti, et al. · EClinicalMedicine · 49
PDF
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy
2013 · Teresa Esposito, Simone Sampaolo, et al. · Orphanet Journal of Rare Diseases · 49
PDF
Spinal muscular atrophy in the era of newborn screening: how the classification could change
2025 · Antonio Varone, Gabriella Esposito, et al. · Frontiers in Neurology · 21
PDF
Motor and neurocognitive profiles of children with symptomatic spinal muscular atrophy type 1 with two copies of SMN2 before and after treatment: a longitudinal observational study
2024 · Ilaria Bitetti, Maria Rosaria Manna, et al. · Frontiers in Neurology · 21
PDF
Cytogenetic evaluation of isochromosome 17q in posterior fossa tumors of children and correlation with clinical outcome in medulloblastoma
2002 · Carolina DeChiara, Annamaria Borghese, et al. · Child s Nervous System · 16
Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016
2024 · Maria Carmela Pera, Giorgia Coratti, et al. · EClinicalMedicine · 15
Malignant cerebral infarction associated with COVID-19 in a child
2021 · Maria Rosaria Scala, Pietro Spennato, et al. · Child s Nervous System · 15
PDF
Neuroendoscopic management of interhemispheric cysts in children
2007 · Giuseppe Cinalli, Paola Peretta, et al. · Neurosurgical FOCUS · 14
PDF
De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling
2023 · Manuela Morleo, Rossella Venditti, et al. · The American Journal of Human Genetics · 12
Is Covid-19 lockdown related to an increase of accesses for seizures in the emergency department? An observational analysis of a paediatric cohort in the Southern Italy
2020 · Federica Palladino, Eugenio Merolla, et al. · Neurological Sciences · 11
PDF
Neuropsychiatric syndrome with myoclonus after SARS-CoV-2 infection in a paediatric patient
2022 · M. Della Corte, C. Delehaye, et al. · Clinical Neurology and Neurosurgery · 10
PDF
Aicardi and Turner syndrome in a 45,X0/46,XX female
2012 · Pietro Spennato, Alessandro La Porta, et al. · Clinical Neurology and Neurosurgery · 10
Acute cerebellar ataxia in children
1997 · Giuseppe Maggi, Antonio Varone, et al. · Child s Nervous System · 10
Subacute sclerosing panencephalitis as a re-emerging condition due to low vaccination coverage: a case-series
2025 · Gabriella Errichiello, Francesco Tengattini, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 9
PDF
Early treatment with Ataluren of a 2-year-old boy with nonsense mutation Duchenne dystrophy.
2021 · Ilaria Bitetti, Cinzia Mautone, et al. · PubMed Central · 7
PDF
Argo Delphi consensus statement on red flags and clinical gateways towards rare disease diagnosis
2025 · Giuseppe Limongelli, Fabio De Iaco, et al. · Scientific Reports · 6
PDF
HPDL Biallelic Variants in Cerebral Palsy and Childhood‐Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights
2025 · Serena Mero, Sara Satolli, et al. · Movement Disorders · 6
PDF
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey
2024 · Anna Capasso, Gianpaolo Cicala, et al. · European Journal of Pediatrics · 5
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus
2024 · Roberta Roberti, Antonella Riva, et al. · Expert Review of Neurotherapeutics · 5
PDF
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
2023 · Emanuele Monda, Michele Lioncino, et al. · International Journal of Molecular Sciences · 5
PDF
Works count: 63
Citation count: 633
H-index: 13
I10-index: 18
Year
Topic
Type