Sfoglia per Autore
A pilot study of a ketogenic diet in patients with Lafora body disease
2006 S. Cardinali, L. Canafoglia, S. Bertoli, S. Franceschetti, G. Lanzi, A. Tagliabue, P. Veggiotti
Auditory attention at the onset of West syndrome: correlation with EEG patterns and visual function
2006 G. Baranello, T. Randò, A. Bancale, M. D'Acunto, R. Epifanio, M. Frisone, A. Guzzetta, G. La Torre, A. Mannocci, D. Ricci, S. Signorini, F. Tinelli, E. Biagioni, P. Veggiotti, E. Fazzi, E. Mercuri, G. Cioni, F. Guzzetta
Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients
2006 G. Capovilla, A. Gambardella, G. Rubboli, F. Beccaria, A. Montagnini, U. Aguglia, M. Canevini, S. Casellato, T. Granata, F. Paladin, A. Romeo, G. Stranci, P. Tinuper, P. Veggiotti, G. Avanzini, C. Tassinari
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families
2006 P. Striano, M. Lispi, E. Gennaro, F. Madia, M. Traverso, L. Bordo, P. Aridon, F. Martinelli Boneschi, B. Barone, B. dalla Bernardina, A. Bianchi, G. Capovilla, P. De Marco, O. Dulac, R. Gaggero, A. Gambardella, R. Nabbout, J. Prud'Homme, R. Day, F. Vanadia, M. Vecchi, P. Veggiotti, F. Vigevano, M. Viri, C. Minetti, F. Zara
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case
2006 S. Orcesi, K. Gorni, C. Termine, C. Uggetti, P. Veggiotti, F. Carrara, M. Zeviani, A. Berardinelli, G. Lanzi
The ketogenic diet: from molecular mechanisms to clinical effects
2006 J. Freeman, P. Veggiotti, G. Lanzi, A. Tagliabue, E. Perucca
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations
2006 M. Mancardi, P. Striano, E. Gennaro, F. Madia, R. Paravidino, S. Scapolan, B. Dalla Bernardina, E. Bertini, A. Bianchi, G. Capovilla, F. Darra, M. Elia, E. Freri, G. Gobbi, T. Granata, R. Guerrini, C. Pantaleoni, A. Parmeggiani, A. Romeo, M. Santucci, M. Vecchi, P. Veggiotti, F. Vigevano, A. Pistorio, R. Gaggero, F. Zara
Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients
2006 G. Capovilla, A. Gambardella, G. Rubboli, F. Beccaria, A. Montagnini, U. Aguglia, M.P. Canevini, S. Casellato, T. Granata, F. Paladin, A. Romeo, G. Stranci, P. Tinuper, P. Veggiotti, G. Avanzini, C.A. Tassinari
Evaluation of nutritional status in children with refractory epilepsy
2006 S. Bertoli, S. Cardinali, P. Veggiotti, C. Trentani, G. Testolin, A. Tagliabue
Uncovering the neural correlates of the ketogenic diet: the contribution of functional neuroimaging
2007 P. Fusar-Poli, M. Cortesi, P. Veggiotti
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis
2007 P. Fusar-Poli, J. Perez, M. Broome, S. Borgwardt, A. Placentino, E. Caverzasi, M. Cortesi, P. Veggiotti, P. Politi, F. Barale, P. Mcguire
Ketogenic Diet: Electrophysiological Effects on the Normal Human Cortex
2007 R. Cantello, C. Varrasi, R. Tarletti, M. Cecchin, F. D'Andrea, P. Veggiotti, G. Bellomo, F. Monaco
Lafora disease : spectroscopy study correlated with neuropsychological findings
2008 A. Pichiecchio, P. Veggiotti, S. Cardinali, F. Longaretti, G. Poloni, C. Uggetti
Cryptogenic Epileptic Syndromes Related to SCN1A Twelve Novel Mutations Identified
2008 C. Zucca, F. Redaelli, R. Epifanio, N. Zanotta, A. Romeo, M. Lodi, P. Veggiotti, G. Airoldi, C. Panzeri, R. Romaniello, G. De Polo, P. Bonanni, S. Cardinali, C. Baschirotto, L. Martorell, R. Borgatti, N. Bresolin, M.T. Bassi
Long-term cognitive and behavioural follow-up in three patients with eye closure-triggered paroxysmal activity
2008 C. Termine, F. Teutonico, U. Balottin, M. Fasce, M. Ferri, S. Perna, P. Piccinelli, G. Rubboli, P. Veggiotti
Neurodevelopmental evolution of West syndrome : a 2-year prospective study
2008 F. Guzzetta, G. Cioni, E. Mercuri, E. Fazzi, E. Biagioni, P. Veggiotti, A. Bancale, G. Baranello, R. Epifanio, M. Frisone, A. Guzzetta, G. La Torre, A. Mannocci, T. Randò, D. Ricci, S. Signorini, F. Tinelli
Evidence of thalamic gray matter loss in pediatric multiple sclerosis
2008 S. Mesaros, M. Rocca, M. Absinta, A. Ghezzi, N. Milani, L. Moiola, P. Veggiotti, G. Comi, M. Filippi
MeCP2 investigation in a wide cohort of italian Rett patients and array methylation assay in six cases sharing the 1164_1027del44 MeCP2 mutation
2009 S. Russo, R. Lupi, M. Marchi, M. Masciadri, I. Moroni, L. Angelini, L. Giordano, P. Veggiotti, F. Cogliati, M.T. Bonati, L. Larizza
THE ELECTROCLINICAL SEIZURE PATTERN OF BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES IN 30 PATIENTS
2009 G. Capovilla, F. Beccaria, A. Bianchi, M. Canevini, B. Frassine, L. Giordano, G. Gobbi, M. Mastrangelo, C. Peruzzi, T. Pisano, P. Striano, P. Veggiotti, A. Vignoli, D. Pruna
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia
2009 P. De Filippi, M. Zecca, D. Lisini, V. Rosti, C. Cagioni, C. Carlo-Stella, O. Radi, P. Veggiotti, A. Mastronuzzi, A. Acquaviva, A. D’Ambrosio, F. Locatelli, C. Danesino
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