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Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, ... Neurology 60 (12), 1961-1967, 2003 | 329 | 2003 |
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy H Stamberger, M Nikanorova, MH Willemsen, P Accorsi, M Angriman, ... Neurology 86 (10), 954-962, 2016 | 316 | 2016 |
Recommendations for the management of “febrile seizures” Ad hoc Task Force of LICE Guidelines Commission G Capovilla, M Mastrangelo, A Romeo, F Vigevano Epilepsia 50, 2-6, 2009 | 258 | 2009 |
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Conservative treatment of thoracic outlet syndrome C Vanti, L Natalini, A Romeo, D Tosarelli, P Pillastrini Eura medicophys 43, 55-70, 2007 | 157 | 2007 |
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Grey‐scale analysis allows a quantitative evaluation of thyroid echogenicity in the patients with Hashimoto's thyroiditis G Mazziotti, F Sorvillo, S Iorio, A Carbone, A Romeo, M Piscopo, ... Clinical endocrinology 59 (2), 223-229, 2003 | 116 | 2003 |
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity M Malacarne, E Gennaro, F Madia, S Pozzi, D Vacca, B Barone, ... The American Journal of Human Genetics 68 (6), 1521-1526, 2001 | 106 | 2001 |
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype–phenotype correlations P Striano, MM Mancardi, R Biancheri, F Madia, E Gennaro, R Paravidino, ... Epilepsia 48 (6), 1092-1096, 2007 | 103 | 2007 |
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences A Labate, P Tarantino, M Viri, L Mumoli, M Gagliardi, A Romeo, F Zara, ... Epilepsia 53 (12), e196-e199, 2012 | 97 | 2012 |
Management of psychogenic non‐epileptic seizures: a multidisciplinary approach S Gasparini, E Beghi, E Ferlazzo, M Beghi, V Belcastro, KP Biermann, ... European journal of neurology 26 (2), 205-e15, 2019 | 93 | 2019 |
68Ga-PSMA PET/CT in patients with recurrent prostate cancer after radical treatment: prospective results in 314 patients P Caroli, I Sandler, F Matteucci, U De Giorgi, L Uccelli, M Celli, F Foca, ... European journal of nuclear medicine and molecular imaging 45, 2035-2044, 2018 | 93 | 2018 |
Requirement of b-myb function for survival and differentiative potential of human neuroblastoma cells G Raschell, A Negroni, A Sala, S Pucci, A Romeo, B Calabretta Journal of Biological Chemistry 270 (15), 8540-8545, 1995 | 89 | 1995 |
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome) P Striano, V Sofia, G Capovilla, G Rubboli, C Di Bonaventura, A Coppola, ... Epilepsia 49 (3), 425-430, 2008 | 88 | 2008 |
Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients G Capovilla, A Gambardella, G Rubboli, F Beccaria, A Montagnini, ... Epilepsia 47 (3), 529-533, 2006 | 83 | 2006 |
Knowledge and attitudes toward epilepsy among primary and secondary schoolteachers in Italy O Mecarelli, G Capovilla, A Romeo, G Rubboli, P Tinuper, E Beghi Epilepsy & Behavior 22 (2), 285-292, 2011 | 81 | 2011 |
Past and present public knowledge and attitudes toward epilepsy in Italy O Mecarelli, G Capovilla, A Romeo, G Rubboli, P Tinuper, E Beghi Epilepsy & Behavior 18 (1-2), 110-115, 2010 | 79 | 2010 |