Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group EH Kossoff, BA Zupec‐Kania, PE Amark, KR Ballaban‐Gil, ... Epilepsia 50 (2), 304-317, 2009 | 732 | 2009 |
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group EH Kossoff, BA Zupec‐Kania, S Auvin, KR Ballaban‐Gil, ... Epilepsia open 3 (2), 175-192, 2018 | 596 | 2018 |
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis P Fusar-Poli, J Perez, M Broome, S Borgwardt, A Placentino, E Caverzasi, ... Neuroscience & Biobehavioral Reviews 31 (4), 465-484, 2007 | 383 | 2007 |
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations E Parrini, A Ramazzotti, WB Dobyns, D Mei, F Moro, P Veggiotti, C Marini, ... Brain 129 (7), 1892-1906, 2006 | 378 | 2006 |
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 | 333 | 2003 |
The ketogenic diet: from molecular mechanisms to clinical effects J Freeman, P Veggiotti, G Lanzi, A Tagliabue, E Perucca Epilepsy Res 68 (2), 145-80, 2006 | 310 | 2006 |
Post-operative benefits of animal-assisted therapy in pediatric surgery: A randomised study V Calcaterra, P Veggiotti, C Palestrini, V De Giorgis, R Raschetti, ... PloS one 10 (6), e0125813, 2015 | 230 | 2015 |
GLUT1 deficiency syndrome 2013: current state of the art V De Giorgis, P Veggiotti Seizure 22 (10), 803-811, 2013 | 227 | 2013 |
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome VL Sheen, A Jansen, MH Chen, E Parrini, T Morgan, R Ravenscroft, ... Neurology 64 (2), 254-262, 2005 | 211 | 2005 |
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 210 | 2019 |
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group J Klepper, C Akman, M Armeno, S Auvin, M Cervenka, HJ Cross, ... Epilepsia open 5 (3), 354-365, 2020 | 205 | 2020 |
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience G Coppola, P Veggiotti, R Cusmai, S Bertoli, S Cardinali, C Dionisi-Vici, ... Epilepsy research 48 (3), 221-227, 2002 | 185 | 2002 |
Evidence of thalamic gray matter loss in pediatric multiple sclerosis S Mesaros, MA Rocca, M Absinta, A Ghezzi, N Milani, L Moiola, ... Neurology 70 (13_part_2), 1107-1112, 2008 | 177 | 2008 |
Treatment of electrical status epilepticus in sleep: a pooled analysis of 575 cases B Van Den Munckhof, V Van Dee, L Sagi, RH Caraballo, P Veggiotti, ... Epilepsia 56 (11), 1738-1746, 2015 | 159 | 2015 |
The phenotype of SCN8A developmental and epileptic encephalopathy E Gardella, C Marini, M Trivisano, MP Fitzgerald, M Alber, KB Howell, ... Neurology 91 (12), e1112-e1124, 2018 | 155 | 2018 |
Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies S Masnada, UBS Hedrich, E Gardella, J Schubert, C Kaiwar, EW Klee, ... Brain 140 (9), 2337-2354, 2017 | 155 | 2017 |
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients F Ragona, T Granata, BD Bernardina, F Offredi, F Darra, D Battaglia, ... Epilepsia 52 (2), 386-392, 2011 | 154 | 2011 |
Mutations in PROSC disrupt cellular pyridoxal phosphate homeostasis and cause vitamin-B6-dependent epilepsy N Darin, E Reid, L Prunetti, L Samuelsson, RA Husain, M Wilson, ... The American Journal of Human Genetics 99 (6), 1325-1337, 2016 | 153 | 2016 |
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance F Zara, N Specchio, P Striano, A Robbiano, E Gennaro, R Paravidino, ... Epilepsia 54 (3), 425-436, 2013 | 153 | 2013 |
Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial G Coppola, G Capovilla, A Montagnini, A Romeo, M Spanò, G Tortorella, ... Epilepsy research 49 (1), 45-48, 2002 | 153 | 2002 |