VIGNOLI, AGLAIA
VIGNOLI, AGLAIA
Dipartimento di Scienze della Salute
Behind the seizures: Exploring the emotional burden of adolescents with idiopathic generalized epilepsy
2026 M.P. Zanaboni, A. Raspanti, C.A. Quaranta, M.S. Bova, M. Celario, M.M. Mensi, G. Milito, F.F. Operto, L. Pasca, G.M.G. Pastorino, F. Raviglione, M. Vedana, A. Vignoli, V. De Giorgis
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitors
2026 I. Musante, G. Gorrieri, S. Tamburro, G. Ferrera, S. Baldassari, A. Fetta, S.G. Caraffi, A. Vignoli, G. Fiorito, L. Garavelli, M.P. Canevini, D.M. Cordelli, F. Zara, E. Ricci, P. Scudieri
Targeting the gut to improve seizure control in CDKL5 deficiency disorder (CDD): study protocol for a single-arm, open-label clinical trial
2025 F. Triva, E. Borghi, M.D. Marsiglia, E. Ottaviano, E. Ricci, P. Tognini, M. Montecucco, A. Vignoli
Acceptance of virtual reality to promote attention orientation in children: a qualitative study among children with ADHD and neurotypical development
2025 G. Bernardelli, S. Arlati, A. Scaglione, E. Saligari, P. Frigerio, A. Sotgiu, V. Flori, D. Lucini, A. Vignoli, A. Zangiacomi
Adjunctive Brivaracetam in People with Epilepsy and Intellectual Disability: Evidence from the BRIVAracetam Add-On First Italian netwoRk Study
2025 S. Lattanzi, L. Canafoglia, M.P. Canevini, S. Casciato, E.C. Irelli, V. Chiesa, F. Dainese, G. De Maria, G. Didato, G. Di Gennaro, G. Falcicchio, M. Fanella, E. Ferlazzo, M. Gangitano, A. La Neve, O. Mecarelli, E. Montalenti, A. Morano, F. Piazza, C. Pizzanelli, P. Pulitano, F. Ranzato, E. Rosati, L. Tassi, C. Di Bonaventura, L. Zumm, E. Zambrelli, F. Villani, A. Vignoli, E. Viglietta, I. Viganò, M. Ventura, A.E. Vaudano, G. Tumminelli, M. Tombini, E. Tartara, D. Stokelj, M. Sessa, E. Savastano, E.M. Salamone, A. Rum, G.R. Rizzo, R. Renna, R. Quintas, P.P. Quarato, S. Quadri, M. Puligheddu, S. Pradella, V. Porcella, P. Pollicino, F. Placidi, L.R. Pisani, F. Pisani, N. Pilolli, P. Pignatta, M. Piccioli, M. Pezzella, G. Perri, A. Peretti, G. Pauletto, C. Pastori, M.G. Pascarella, F. Paladin, B. Orlando, A. Nilo, C. Milano, S. Meletti, A. Mazzeo, A. Mascia, D. Marino, L. Mari, G. Maira, M. Magliani, C. Luisi, A. Labate, B. Kassabian, F. Izzi, F. Habetswallner, L. Giuliano, F.S. Giorgi, A.T. Giallonardo, S. Gazzina, R. Galli, T. Francavilla, N. Foschi, F. Fortunato, D. Fonti, G. Fisco, F. Ferreri, A. Ferrari, J. Fattouch, E. Fallica, Y. Failli, M.T. Faedda, G. Evangelista, A. Estraneo, M. Elia, V. Durante, F. Dono, E. Domina, A.R.D. Liberto, R.D. Giacomo, J.C. Difrancesco, F. Deleo, A. D’Aniello, E. Cumbo, C. Costa, M. Contento, D. Colella, D. Cocito, R. Ciuffini, D. Ciampanelli, G. Chianale, E. Cesnik, C. Calvello, C. Cagnetti, E. Caggia, F. Brigo, J. Bongiorno, P. Bonanni, G. Boero, G. Billo, M. Biggi, I. Berto, S. Beretta, V. Belcastro, L.M. Basili, E. Bartolini, P. Banfi, V. Badioni, F. Avorio, G. Assenza, M. Ascoli, A. Alicino
Publisher Correction: Rett syndrome
2025 W.A. Gold, A.K. Percy, J.L. Neul, S.R. Cobb, L. Pozzo-Miller, J.K. Issar, B. Ben-Zeev, A. Vignoli, W.E. Kaufmann
Developmental and epileptic encephalopathies: From current care to future perspectives - insights from epilepsy centres in Lombardy, Italy
2025 G. Didato, F. Ragona, A. Pompili, F. Beccaria, S. Beretta, V. Chiesa, V.D. Giorgis, G.D. Maria, R. Dilena, I.L. Giordano, F. Labriola, M. Lodi, C. Peruzzi, R. Quintas, C. Zucca, A. Vignoli
Clinical and genetic landscape of epilepsies with absence seizures and single‐gene etiology
2025 B. Simona, G. Ilaria, R. Maria Luisa, P. Elena, M. Davide, M. Mario, P. Francesco, F. Corinna, G. Lucio, C. Elisabetta, M. Carla, C.I. Emanuele, D.B. Carlo, R. Marica, C. Antonietta, P. Jacopo, B. Tommaso Lo, D. Francesca, L. Laura, B. Francesca, P. Marco, B. Domenica, D.D. Angela, T. Marina, S. Nicola, S. Roberta, C. Davide, C. Laura, G. Renzo, L. Collaborative Group: Carmen Barba, E. Bartolini, P. Bernardo, M.P. Canevini, G. Cantalupo, S. Casellato, M. Cavallin, I. Contaldo, A. Ferretti, M. Luigia Gambardella, T. Granata, G. Lentini, A. Luchetti, F. Melani, P. Parisi, S. Pellacani, L. Pietrangelo, T. Pisano, I. Onida, E. Ricci, A. Vignoli
Is highly purified cannabidiol a treatment opportunity for drug‐resistant epilepsy in subjects with typical Rett syndrome and CDKL5 deficiency disorder?
2025 A. Vignoli, G. Prato, E. Alfei, I. Bagnasco, A. Danieli, M. Celario, J. Favaro, S. Matricardi, F.F. Operto, A. Orsini, D.P. Bernasconi, N. Pietrafusa, E. Ricci, L. Manfredini, G. Balletto, P. Bonanni, M.P. Canevini, V. De Giorgis, L. Nobili, S. Sartori, M.N. Savini, I. Viganò, N. Specchio
Prediction of evolution to epilepsy or genetic epilepsy with febrile seizures plus (GEFS+) in children presenting with febrile seizures: a retrospective multicenter longitudinal study
2025 P. Baso, S. Masnada, M.M. Lodi, F. Teutonico, A. Vignoli, E. Ricci, M.P. Canevini, F. Brustia, M. Viri, C. Cereda, L. Lalli, S. Ferraro, P. Veggiotti
Tuberous sclerosis complex, epilepsy, and the microbiota-gut-brain axis: a pilot study of shared and divergent microbial signatures
2025 E. Ottaviano, M.D. Marsiglia, C. Ceccarani, S. Ancona, F. Triva, F. La Briola, S. Bergamoni, F. Teutonico, A. Pompili, I. Viganò, E. Ricci, A. Vignoli, E. Borghi
SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder
2025 M.M.K. Wong, R.A. Kampen, R.O. Braden, G. Alagöz, M.S. Hildebrand, A.J.M. Dingemans, J. Corbally, J. Den Hoed, E. Mendoza, W.J.J. Claassen, C. Barnett, M. Barnett, A. Brusco, D. Carli, B.B.A. De Vries, F. Elmslie, G.B. Ferrero, N.A. Jansen, I.M.B.H. Van De Laar, A. Moroni, D. Mowat, L. Murray, F. Novara, A. Peron, I.E. Scheffer, F. Sirchia, S.J. Turner, A. Vignoli, A. Vino, S. Weber, W.K. Chung, M. Gerard, V. López-González, E. Palmer, A.T. Morgan, B.W. Van Bon, S.E. Fisher
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
Natural history of adults with KBG syndrome: a physician-reported experience
2024 A. Bayat, H. Grimes, E. de Boer, M.K. Herlin, R.S. Dahl, I.C.B. Lund, M. Bayat, A.C. Skjelmose Bolund, C.E. Gjerulfsen, P.A. Gregersen, M. Zilmer, S. Juhl, K. Cebula, E. Rahikkala, I. Maystadt, A. Peron, A. Vignoli, R.M. Alfano, F. Stanzial, F. Benedicenti, A. Currò, H. Luk, G. Jouret, E. Zurita, L. Heuft, F. Schnabel, A. Busche, H.E. Veenstra-Knol, T. Tkemaladze, P. Vrielynck, D. Lederer, K. Platzer, C.W. Ockeloen, H. Goel, K.J. Low
Myoclonus: Differential diagnosis and current management
2024 A. Riva, G. D'Onofrio, E. Ferlazzo, A. Pascarella, E. Pasini, S. Franceschetti, F. Panzica, L. Canafoglia, A. Vignoli, A. Coppola, V. Badioni, F. Beccaria, A. Labate, A. Gambardella, A. Romeo, G. Capovilla, R. Michelucci, P. Striano, V. Belcastro
Continuous spike-wave of slow sleep in a patient with KCNB1-related epilepsy responsive to highly purified cannabidiol: a case report and comparison with literature
2024 G. Ferrera, E. Ricci, A. Peron, E. Parrini, A. Vignoli, M.P. Canevini
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
Early onset epileptic and developmental encephalopathy and MOGS variants: a new diagnosis in the whole exome sequencing (WES) ERA : Report of a new patient and review of the literature
2024 F. Teutonico, C. Volpe, A. Proto, I. Costi, U. Cavallari, P. Doneda, M. Iascone, L. Sturiale, R. Barone, S. Martinelli, A. Vignoli
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders
2024 J. Sidpra, S. Sudhakar, A. Biswas, F. Massey, V. Turchetti, T. Lau, E. Cook, J.R. Alvi, H.M. Elbendary, J.L. Jewell, A. Riva, A. Orsini, A. Vignoli, Z. Federico, J. Rosenblum, A. Schoonjans, M. de Wachter, I. Delgado Alvarez, A. Felipe-Rucián, N.A. Haridy, S. Haider, M. Zaman, S. Banu, N. Anwaar, F. Rahman, S. Maqbool, R. Yadav, V. Salpietro, R. Maroofian, R. Patel, R. Radhakrishnan, S.P. Prabhu, K. Lichtenbelt, H. Stewart, Y. Murakami, U. Löbel, F. D'Arco, E. Wakeling, W. Jones, E. Hay, S. Bhate, T.S. Jacques, D.M. Mirsky, M.T. Whitehead, M.S. Zaki, T. Sultan, P. Striano, A.C. Jansen, M. Lequin, L.S. de Vries, M. Severino, A.C. Edmondson, L. Menzies, P.M. Campeau, H. Houlden, A. Mctague, S. Efthymiou, K. Mankad
Rett syndrome
2024 W.A. Gold, A.K. Percy, J.L. Neul, S.R. Cobb, L. Pozzo-Miller, J.K. Issar, B. Ben-Zeev, A. Vignoli, W.E. Kaufmann