Get started
Author

Francesca Beccaria

Observed name: F. Beccaria
Observed institutions: University of Messina, University of Zurich, University of Pavia, Istituto Giannina Gaslini, Magna Graecia University, Fondazione Istituto Neurologico Nazionale Casimiro Mondino, Azienda ospedaliera "Bianchi-Melacrino-Morelli", Institute of Neurological Sciences, University Children's Hospital Zurich, Ospedale San Donato, Fondazione Poliambulanza Istituto Ospedaliero, Azienda Ospedaliera Fatebenefratelli e Oftalmico, Policlinico San Matteo Fondazione, Fondazione IRCCS Istituto Neurologico Carlo Besta, Azienda Ospedaliera Carlo Poma, Aziende Socio Sanitarie Territoriale Lodi, University of Genoa, Sapienza University of Rome
ORCID: 0000-0003-0794-1172
Observed ORCID: 0000-0003-0794-1172
OpenAlex ID: A5015830625
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance
2013 · Federico Zara, Nicola Specchio, et al. · Epilepsia · 128
PDF
Suppressive Efficacy by a Commercially Available Blue Lens on PPR in 610 Photosensitive Epilepsy Patients
2006 · Giuseppe Capovilla, Antonio Gambardella, et al. · Epilepsia · 101
Continuous Spike‐and‐Wave Activity During Slow‐Wave Sleep: Syndrome or EEG Pattern?
1999 · Pierangelo Veggiotti, Francesca Beccaria, et al. · Epilepsia · 99
Increased cortical BOLD signal anticipates generalized spike and wave discharges in adolescents and adults with idiopathic generalized epilepsies
2012 · Francesca Benuzzi, Laura Mirandola, et al. · Epilepsia · 97
Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations
2007 · Pasquale Striano, Maria Margherita Mancardi, et al. · Epilepsia · 92
Treatment of convulsive status epilepticus in childhood: Recommendations of the I talian L eague A gainst E pilepsy
2013 · Giuseppe Capovilla, Francesca Beccaria, et al. · Epilepsia · 81
PDF
Confirmation of mutations in PROSC as a novel cause of vitamin B 6 -dependent epilepsy
2017 · Barbara Plecko, Markus Zweier, et al. · Journal of Medical Genetics · 78
The spectrum of benign myoclonus of early infancy: Clinical and neurophysiologic features in 102 patients
2009 · Roberto H. Caraballo, Giuseppe Capovilla, et al. · Epilepsia · 69
PDF
Benign convulsions associated with mild gastroenteritis: A multicenter clinical study
2010 · Alberto Verrotti, Giuliana Nanni, et al. · Epilepsy Research · 68
Photosensitivity: epidemiology, genetics, clinical manifestations, assessment, and management
2012 · Alberto Verrotti, Francesca Beccaria, et al. · Epileptic Disorders · 64
Paediatric anti-N-methyl-d-aspartate receptor encephalitis: The first Italian multicenter case series
2015 · Stefano Sartori, Margherita Nosadini, et al. · European Journal of Paediatric Neurology · 59
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy
2011 · Ida Manna, Antonio Gambardella, et al. · Epilepsia · 58
PDF
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia
2009 · Giuseppe Capovilla, Pasquale Striano, et al. · Epilepsia · 55
Myoclonus: Differential diagnosis and current management
2024 · Antonella Riva, Gianluca D'Onofrio, et al. · Epilepsia Open · 53
PDF
Mutational Analysis of EFHC1 Gene in Italian Families with Juvenile Myoclonic Epilepsy
2007 · Ferdinanda Annesi, Antonio Gambardella, et al. · Epilepsia · 52
Epilepsy Course and Developmental Trajectories in STXBP1 -DEE
2022 · Ganna Balagura, Julie Xian, et al. · Neurology Genetics · 49
PDF
Continuous spikes and waves during sleep in children with shunted hydrocephalus
1998 · P. Veggiotti, F. Beccaria, et al. · Child s Nervous System · 46
Genome‐wide linkage meta‐analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
2012 · Costin Leu, Carolien G.F. de Kovel, et al. · Epilepsia · 40
PDF
Two novel ALDH7A1 (antiquitin) splicing mutations associated with pyridoxine‐dependent seizures
2008 · Pasquale Striano, Silvia Battaglia, et al. · Epilepsia · 40
Benign partial epilepsy in infancy and early childhood with vertex spikes and waves during sleep: a new epileptic form
2000 · Giuseppe Capovilla, Francesca Beccaria · Brain and Development · 40
Ethosuximide Is Effective in the Treatment of Epileptic Negative Myoclonus in Childhood Partial Epilepsy
1999 · Giuseppe Capovilla, Francesca Beccaria, et al. · Journal of Child Neurology · 40
Photosensitive Benign Myoclonic Epilepsy in Infancy
2006 · Giuseppe Capovilla, Francesca Beccaria, et al. · Epilepsia · 39
PDF
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video‐polygraphic study
2001 · Giuseppe Capovilla, Guido Rubboli, et al. · Epileptic Disorders · 39
Long-term follow-up in children with benign convulsions associated with gastroenteritis
2014 · Alberto Verrotti, Romina Moavero, et al. · European Journal of Paediatric Neurology · 38
Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht‐Lundborg disease carrying compound heterozygous CSTB point and indel mutations
2012 · Laura Canafoglia, Elena Gennaro, et al. · Epilepsia · 38
Works count: 59
Citation count: 1,976
H-index: 28
I10-index: 44
Year
Topic
Type