VEGGIOTTI, PIERANGELO
VEGGIOTTI, PIERANGELO
Dipartimento di Scienze Biomediche e Cliniche
The expanding knowledge of epilepsy in leukodystrophies
2024 Y. Vaia, E. Minacapilli, S. Masnada, P. Veggiotti, D. Tonduti, M.A.M. Lodi
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
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
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
Eating disorder risks and psychopathological distress in Italian high school adolescents
2024 V. Calcaterra, V.C. Magenes, M. Basso, V. Conte, G. Maggioni, S. Russo, A. De Silvestri, V. Fabiano, E.A. Marrocco, P. Veggiotti, G. Zuccotti
Long−term health outcome and quality of life in children with multisystem inflammatory syndrome: findings from multidisciplinary 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
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
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
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
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
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
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
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
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
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
Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis
2022 A. Mauri, A. Duse, G. Palm, R. Previtali, S. Bova, S. Olivotto, S. Benedetti, F. Coscia, P. Veggiotti, C. Cereda
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
2022 S. Olivotto, A. Duse, S. Maria Bova, V. Leonardi, E. Biganzoli, A. Milanese, C. Cereda, S. Bertoli, R. Previtali, P. Veggiotti
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
Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity
2022 S. Olivotto, A. Freddi, R. Lavatelli, E. Basso, A. Leidi, B. Castellotti, L. Spaccini, S.M. Bova, P. Veggiotti