VEGGIOTTI, PIERANGELO
VEGGIOTTI, PIERANGELO
Dipartimento di Scienze Biomediche e Cliniche
The influence of wakefulness fluctuations on brain networks involved in centrotemporal spike occurrence
2024 F. Talami, L. Lemieux, P. Avanzini, A. Ballerini, G. Cantalupo, H. Laufs, S. Meletti, A.E. Vaudano, P. Bergonzini, E. Caramaschi, M.P. Canevini, B.D. Bernardina, G. Gobbi, M. Filippini, G. Gessaroli, B. Piccolo, F. Pisani, M. Santucci, P. Veggiotti, A. Vignoli
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study
2024 B. Cavirani, C. Spagnoli, S.G. Caraffi, A. Cavalli, C.A. Cesaroni, G. Cutillo, V. De Giorgis, D. Frattini, G.B. Marchetti, S. Masnada, A. Peron, S. Rizzi, C. Varesio, L. Spaccini, A. Vignoli, M.P. Canevini, P. Veggiotti, L. Garavelli, C. Fusco
Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome
2024 S. Olivotto, A. Freddi, R. Previtali, A. Mauri, C. Cereda, R. De Amicis, S. Bertoli, C. Doneda, P. Veggiotti
Long−term health outcome and quality of life in children with multisystem inflammatory syndrome: findings from multidMEDisciplinary follow−up at an Italian tertiary−care paediatric hospital
2024 E. D'Auria, S.M. Bova, A.R. Dallapiccola, R. De Santis, A. Leone, V. Calcaterra, S. Mannarino, M. Garbin, S. Olivotto, S. Zirpoli, M. Ghezzi, A.M. Munari, E. Verduci, A. Farolfi, A. Bosetti, V. Perico, P. Capetti, A. Gadda, L. Gianolio, G. Lo Monaco, L. Lonoce, R. Previtali, L. Serafini, S. Taranto, P. Veggiotti, G. Zuccotti
Menkes disease complicated by concurrent ACY1 deficiency: A case report
2023 A. Mauri, L.A. Saielli, E. Alfei, M. Iascone, D. Marchetti, E. Cattaneo, A. Di Lauro, L. Antonelli, L. Alberti, E. Bonaventura, P. Veggiotti, L. Spaccini, C. Cereda
A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet
2023 J.C. Difrancesco, F. Ragona, C. Murano, A. Frosio, D. Melgari, A. Binda, S. Calamaio, R. Prevostini, M. Mauri, L. Canafoglia, B. Castellotti, G. Messina, C. Gellera, R. Previtali, P. Veggiotti, R. Milanesi, A. Barbuti, R. Solazzi, E. Freri, T. Granata, I. Rivolta
Paradigm shift in the treatment of tuberous sclerosis: Effectiveness of everolimus
2023 R. Previtali, G. Prontera, E. Alfei, L. Nespoli, S. Masnada, P. Veggiotti, S. Mannarino
Case report: Early-onset parkinsonism among the neurological features in children with PHACTR1 variants
2023 R. Previtali, A. Leidi, M. Basso, G. Izzo, C. Stignani, L. Spaccini, M. Iascone, P. Veggiotti, S.M. Bova
Thyroid dysfunction in children and adolescents affected by undernourished and overnourished eating disorders
2023 V. Calcaterra, V.C. Magenes, F. Siccardo, C. Hruby, M. Basso, V. Conte, G. Maggioni, V. Fabiano, S. Russo, P. Veggiotti, G. Zuccotti
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring
2023 E. Bonaventura, L. Alberti, S. Lucchi, L. Cappelletti, S. Fazzone, E. Cattaneo, M. Bellini, G. Izzo, C. Parazzini, A. Bosetti, E. Di Profio, G. Fiore, M. Ferrario, C. Mameli, A. Sangiorgio, S. Masnada, G.V. Zuccotti, P. Veggiotti, L. Spaccini, M. Iascone, E. Verduci, C. Cereda, D. Tonduti
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders
2023 C. Varesio, V. De Giorgis, P. Veggiotti, N. Nardocci, T. Granata, F. Ragona, L. Pasca, M.M. Mensi, R. Borgatti, S. Olivotto, R. Previtali, A. Riva, M.M. Mancardi, P. Striano, M. Cavallin, R. Guerrini, F.F. Operto, A. Pizzolato, R. Di Maulo, F. Martino, A. Lodi, C. Marini
FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy
2023 S. Masnada, R. Previtali, P. Erba, E. Beretta, A. Camporesi, L. Chiapparini, C. Doneda, M. Iascone, M.U.A. Sartorio, L. Spaccini, P. Veggiotti, M. Osio, D. Tonduti, I. Moroni
Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
2023 R. De Amicis, A. Leone, M. Pellizzari, A. Foppiani, A. Battezzati, C. Lessa, A. Tagliabue, C. Ferraris, V. De Giorgis, S. Olivotto, R. Previtali, P. Veggiotti, S. Bertoli
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study
2023 I. Toldo, F. Brunello, P. Cavasin, M. Nosadini, S. Sartori, A.C. Frigo, R. Mai, V. Pelliccia, M.M. Mancardi, P. Striano, M. Severino, F. Zara, R. Rizzi, S. Casellato, G. Di Rosa, M. Mastrangelo, A. Spalice, M. Budetta, L. De Palma, R. Guerrini, D. Pruna, D.M. Cordelli, V. Sofia, A. Papa, V. Chiesa, F. Ragona, P. Parisi, A. D'Aniello, P. Veggiotti, F. Dainese, L. Giordano, L. Licchetta, P. Tinuper, G. D'Orsi, M. Cassina, R. Manara
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants
2022 G. Berecki, K.B. Howell, J. Heighway, N. Olivier, J. Rodda, I. Overmars, D.R.M. Vlaskamp, T.L. Ware, S. Ardern-Holmes, G. Lesca, M. Alber, P. Veggiotti, I.E. Scheffer, S.F. Berkovic, M. Wolff, S. Petrou
Long-term therapeutic effect of eslicarbazepine acetate in children: An open-label extension of a cognition study in children aged 6–16 years
2022 P. Veggiotti, S. Jozwiak, F. Kirkham, J. Moreira, A. Pereira, F. Ikedo, H. Gama
Seizures may be an early sign of acute COVID-19, and the Omicron variant could present a more epileptogenic profile
2022 S.M. Bova, L. Serafini, I. Serati, L. Fiori, P. Veggiotti
Cognitive, Behavioral and Socioemotional Development in a Cohort of Preterm Infants at School Age: A Cross-Sectional Study
2022 C. Ionio, G. Lista, P. Veggiotti, C. Colombo, G. Ciuffo, I. Daniele, M. Landoni, B. Scelsa, E. Alfei, S. Bova
Safety and efficacy of ganaxolone in patients with CDKL5 deficiency disorder: results from the double-blind phase of a randomised, placebo-controlled, phase 3 trial
2022 E.M.P. Knight, S. Amin, N. Bahi-Buisson, T.A. Benke, J.H. Cross, S.T. Demarest, H.E. Olson, N. Specchio, T.R. Fleming, A.A. Aimetti, M. Gasior, O. Devinsky, E. Belousova, O. Belyaev, B. Ben-Zeev, A. Brunklaus, M.A. Ciliberto, F. Darra, R. Davis, V. De Giorgis, O. Doronina, M. Fahey, R. Guerrini, P. Heydemann, O. Khaletskaya, P. Lisewski, E.D. Marsh, A.N. Moosa, S. Perry, S. Philip, R.R. Rajaraman, B. Renfroe, R.P. Saneto, I.E. Scheffer, Y. Sogawa, B. Suter, M.T. Sweney, D. Tarquinio, P. Veggiotti, G. Wallace, J. Weisenberg, A. Wilfong, E.C. Wirrell, M. Zafar, M. Zolnowska
A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster
2022 G.D. Mangano, V. Antona, E. Cali, A. Fontana, V. Salpietro, H. Houlden, P. Veggiotti, R. Nardello