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S. Grosso · SciRah

Researcher profile · Semantic Scholar

S. Grosso

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S. Grosso — researcher profile on SciRah

h-index: 42
Works: 178
Citations: 5,528

Most-cited papers

Drug Retention Rate and Predictive Factors of Drug Survival for Interleukin-1 Inhibitors in Systemic Juvenile Idiopathic Arthritis
J. Sota, A. Insalaco, R. Cimaz, M. Alessio +16 more
2019Frontiers in Pharmacology348 citations Open access
Semantic Scholar
Oxidative stress in epilepsy
Ursula Geronzi, F. Lotti, S. Grosso
2018Expert Review of Neurotherapeutics183 citations
Semantic Scholar
Withdrawal of antiepileptic drugs: Guidelines of the Italian League Against Epilepsy
E. Beghi, G. Giussani, S. Grosso, A. Iudice +7 more
2013Epilepsia141 citations
Semantic Scholar
Topiramate-induced weight loss: a review.
A. Verrotti, Alessandra Scaparrotta, S. Agostinelli, S. Di Pillo +2 more
2011Epilepsy Research127 citations
Semantic Scholar
Focal seizures with affective symptoms are a major feature of PCDH19 gene–related epilepsy
C. Marini, F. Darra, N. Specchio, D. Mei +21 more
2012Epilepsia78 citations Open access
Semantic Scholar
Acute ataxia in paediatric emergency departments: a multicentre Italian study
Giacomo Garone, A. Reale, N. Vanacore, P. Parisi +25 more
2019Archives of Disease in Childhood71 citations
Semantic Scholar
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study.
A. Verrotti, G. Nanni, S. Agostinelli, P. Parisi +19 more
2011Epilepsy Research67 citations
Semantic Scholar
Treatment options for periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome in children and adults: a narrative review
C. Gaggiano, D. Rigante, J. Sota, S. Grosso +1 more
2018Clinical Rheumatology65 citations
Semantic Scholar
Lacosamide in pediatric and adult patients: comparison of efficacy and safety.
A. Verrotti, Giulia Loiacono, Antonella Pizzolorusso, P. Parisi +21 more
2013Seizure62 citations Open access
Semantic Scholar
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter study.
P. De Liso, F. Vigevano, N. Specchio, L. de Palma +27 more
2016Epilepsy Research61 citations
Semantic Scholar
Efficacy and safety of lacosamide in infants and young children with refractory focal epilepsy.
S. Grosso, P. Parisi, A. Spalice, A. Verrotti +1 more
2014European journal of paediatric neurology54 citations
Semantic Scholar
Rufinamide in children and adults with Lennox-Gastaut syndrome: first Italian multicenter experience.
G. Coppola, S. Grosso, E. Franzoni, P. Veggiotti +11 more
2010Seizure53 citations Open access
Semantic Scholar
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities
S. Matricardi, A. Spalice, V. Salpietro, G. Di Rosa +15 more
2016American Journal of Medical Genetics. Part C, Seminars in Medical Genetics48 citations Open access
Semantic Scholar
Epilepsy and vaccinations: Italian guidelines
D. Pruna, P. Balestri, N. Zamponi, S. Grosso +7 more
2013Epilepsia48 citations Open access
Semantic Scholar
Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype
D. Cordelli, L. Garavelli, S. Savasta, A. Guerra +36 more
2013American Journal of Medical Genetics. Part A48 citations
Semantic Scholar
Seizures and epilepsy in Sotos syndrome: Analysis of 19 Caucasian patients with long‐term follow‐up
F. Nicita, M. Ruggieri, A. Polizzi, L. Mauceri +11 more
2012Epilepsia45 citations Open access
Semantic Scholar
Cyclic Vomiting Syndrome in Children
U. Raucci, O. Borrelli, G. Di Nardo, R. Tambucci +25 more
2020Frontiers in Neurology42 citations Open access
Semantic Scholar
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.
F. Mari, A. Marozza, M. Mencarelli, Caterina Lo Rizzo +22 more
2015Brain & development (Tokyo. 1979)42 citations Open access
Semantic Scholar
Rufinamide in refractory childhood epileptic encephalopathies other than Lennox–Gastaut syndrome
G. Coppola, S. Grosso, E. Franzoni, P. Veggiotti +11 more
2011European Journal of Neurology42 citations
Semantic Scholar
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype.
Annarita Giliberti, Aurora Curró, F. T. Papa, E. Frullanti +5 more
2019European Journal of Medical Genetics37 citations
Semantic Scholar
Refractory absence seizures: An Italian multicenter retrospective study.
E. Franzoni, S. Matricardi, V. Di Pisa, G. Capovilla +22 more
2015European journal of paediatric neurology36 citations Open access
Semantic Scholar
Long-term follow-up in children with benign convulsions associated with gastroenteritis.
A. Verrotti, R. Moavero, F. Vigevano, L. Cantonetti +25 more
2014European journal of paediatric neurology36 citations
Semantic Scholar
Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases
C. Gaggiano, D. Rigante, A. Vitale, O. Lucherini +8 more
2019Mediators of Inflammation35 citations Open access
Semantic Scholar
Anakinra Drug Retention Rate and Predictive Factors of Long-Term Response in Systemic Juvenile Idiopathic Arthritis and Adult Onset Still Disease
J. Sota, D. Rigante, P. Ruscitti, A. Insalaco +29 more
2019Frontiers in Pharmacology34 citations Open access
Semantic Scholar
Oxidative stress in children affected by epileptic encephalopathies.
S. Grosso, M. Longini, Antonello Rodriguez, F. Proietti +3 more
2011Journal of Neurological Sciences34 citations
Semantic Scholar
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience.
S. Grosso, N. Zamponi, A. Bartocci, E. Cesaroni +3 more
2014European journal of paediatric neurology31 citations
Semantic Scholar
Natural history of KBG syndrome in a large European cohort
L. Loberti, L. Bruno, Stefania Granata, Gabriella Doddato +55 more
2022Human Molecular Genetics30 citations Open access
Semantic Scholar
Comparison of Early vs. Delayed Anakinra Treatment in Patients With Adult Onset Still's Disease and Effect on Clinical and Laboratory Outcomes
A. Vitale, G. Cavalli, P. Ruscitti, J. Sota +46 more
2020Frontiers in Medicine30 citations Open access
Semantic Scholar
Epilepsy in patients with Cornelia de Lange syndrome: a clinical series.
A. Verrotti, S. Agostinelli, G. Prezioso, G. Coppola +10 more
2013Seizure30 citations Open access
Semantic Scholar
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.
A. Verrotti, R. Cusmai, F. Nicita, Antonella Pizzolorusso +17 more
2013Jornal de Pediatria29 citations
Semantic Scholar
Dysembryoplastic neuroepithelial tumors: a prospective clinicopathologic and outcome study of 13 children.
A. Spalice, M. Ruggieri, S. Grosso, A. Verrotti +7 more
2010Pediatric Neurology29 citations
Semantic Scholar
The current status of biological treatment for uveitis
C. Gaggiano, J. Sota, S. Gentileschi, V. Caggiano +5 more
2020Expert Review of Clinical Immunology28 citations
Semantic Scholar
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene.
L. Bianciardi, Valentina Imperatore, E. Fernández-Vizarra, A. Lopomo +8 more
2016Molecular Genetics and Metabolism28 citations Open access
Semantic Scholar
Clinical Features at Onset and Genetic Characterization of Pediatric and Adult Patients with TNF-α Receptor—Associated Periodic Syndrome (TRAPS): A Series of 80 Cases from the AIDA Network
C. Gaggiano, A. Vitale, L. Obici, G. Merlini +33 more
2020Mediators of Inflammation27 citations Open access
Semantic Scholar
Management of status dystonicus in children. Cases report and review.
S. Grosso, A. Verrotti, M. Messina, M. Sacchini +1 more
2012European journal of paediatric neurology26 citations
Semantic Scholar
Long term outcome in children affected by absence epilepsy with onset before the age of three years.
A. Verrotti, C. Olivieri, S. Agostinelli, G. Coppola +8 more
2011Epilepsy & Behavior25 citations
Semantic Scholar
Long-term outcome of epilepsy in patients with Prader–Willi syndrome
A. Verrotti, R. Cusmai, D. Laino, R. Falsaperla +19 more
2014Journal of Neurology23 citations
Semantic Scholar
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age.
V. Uliana, S. Grosso, M. Cioni, F. Ariani +11 more
2010European Journal of Medical Genetics22 citations
Semantic Scholar
Recurrent Miller Fisher syndrome in children.
S. Grosso, A. Verrotti, M. Tei, S. Cornacchione +2 more
2014Pediatric Neurology21 citations
Semantic Scholar
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies.
S. Grosso, G. Coppola, Serena Donetti Dontin, G. Gobbi +5 more
2014European journal of paediatric neurology20 citations
Semantic Scholar
Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects
A. Verrotti, C. Soldani, D. Laino, R. d’Alonzo +1 more
2014World Journal of Pediatrics17 citations
Semantic Scholar
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS).
S. Grosso, P. Parisi, L. Giordano, R. D. Di Bartolo +1 more
2014Epilepsy Research16 citations
Semantic Scholar
Correspondence on ‘Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort’
M. V. Mastrolia, R. Agostiniani, C. Azzari, R. Bernardini +18 more
2020Annals of the Rheumatic Diseases15 citations
Semantic Scholar
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy.
S. Grosso, R. Mostardini, R. D. Di Bartolo, P. Balestri +1 more
2011European journal of paediatric neurology15 citations
Semantic Scholar
The Autoinflammatory Diseases Alliance Registry of monogenic autoinflammatory diseases
C. Gaggiano, A. Vitale, A. Tufan, G. Ragab +84 more
2022Frontiers in Medicine14 citations Open access
Semantic Scholar
Treating juvenile idiopathic arthritis (JIA)-related uveitis beyond TNF-α inhibition: a narrative review
C. Gaggiano, D. Rigante, G. Tosi, A. Vitale +4 more
2019Clinical Rheumatology14 citations
Semantic Scholar
CKAP2L mutation confirms the diagnosis of Filippi syndrome
G. Capecchi, M. Baldassarri, S. Ferranti, E. Guidoni +5 more
2018Clinical Genetics14 citations
Semantic Scholar
17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization
C. Romano, S. Ferranti, M. Mencarelli, I. Longo +2 more
2020Neurological Sciences13 citations
Semantic Scholar
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum.
S. Grosso, M. Carluccio, E. Cardaioli, A. Cerase +4 more
2017Brain & development (Tokyo. 1979)11 citations
Semantic Scholar
Valproate in adolescents with photosensitive epilepsy with generalized tonic-clonic seizures only.
A. Verrotti, S. Grosso, C. D’Egidio, P. Parisi +4 more
2014European journal of paediatric neurology11 citations
Semantic Scholar

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A. Spalice×17
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A. Spalice — researcher profile on SciRah
P. Balestri×13
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N. Zamponi — researcher profile on SciRah

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E. Franzoni×11

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A. Renieri — researcher profile on SciRah

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C. Gaggiano — researcher profile on SciRah

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