Pierangelo Veggiotti
Pierangelo Veggiotti
Verified email at unipv.it
TitleCited byYear
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
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
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
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
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
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
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
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 Span˛, G Tortorella, ...
Epilepsy research 49 (1), 45-48, 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
Continuous spike‐and‐wave activity during slow‐wave sleep: syndrome or EEG pattern?
P Veggiotti, F Beccaria, R Guerrini, G Capovilla, G Lanzi
Epilepsia 40 (11), 1593-1601, 1999
GLUT1 deficiency syndrome 2013: current state of the art
V De Giorgis, P Veggiotti
Seizure 22 (10), 803-811, 2013
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy
E Gennaro, FM Santorelli, E Bertini, D Buti, R Gaggero, G Gobbi, M Lini, ...
Biochemical and biophysical research communications 341 (2), 489-493, 2006
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
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
P Bonanni, M Malcarne, F Moro, P Veggiotti, D Buti, AR Ferrari, E Parrini, ...
Epilepsia 45 (2), 149-158, 2004
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
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
Lamotrigine in infantile spasms
P Veggiotti, C Cieuta, E Rey, O Dulac
The Lancet 344 (8933), 1375-1376, 1994
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients
F Ragona, D Brazzo, I De Giorgi, M Morbi, E Freri, F Teutonico, ...
Brain and Development 32 (1), 71-77, 2010
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene
F Moro, R Carrozzo, P Veggiotti, G Tortorella, D Toniolo, A Volzone, ...
Neurology 58 (6), 916-921, 2002
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study
A Verrotti, G Nanni, S Agostinelli, P Parisi, G Capovilla, F Beccaria, ...
Epilepsy research 93 (2-3), 107-114, 2011
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