VIGNOLI, AGLAIA
VIGNOLI, AGLAIA
Dipartimento di Scienze della Salute
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
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
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
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
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
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
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
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
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
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children
2024 A. Fetta, F. Toni, I. Pettenuzzo, E. Ricci, A. Rocca, C. Gambi, L. Soliani, V. Di Pisa, S. Martini, G. Sperti, V. Cagnazzo, P. Accorsi, E. Bartolini, D. Battaglia, P. Bernardo, M.P. Canevini, A.R. Ferrari, L. Giordano, C. Locatelli, M. Mancardi, A. Orsini, T. Pippucci, D. Pruna, A. Rosati, A. Suppiej, S. Tagliani, A. Vaisfeld, A. Vignoli, K. Izumi, I. Krantz, D.M. Cordelli
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
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
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
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
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
Psychogenic non-epileptic seizures in individuals with intellectual disability/borderline cognitive function: Characterization through a comparison study
2024 E. Ricci, K. Turner, E. De Ponti, G. Ferrera, E. Zambrelli, G. Tumminelli, M. Canevini, A. Vignoli, V. Chiesa
24-h continuous non-invasive multiparameter home monitoring of vitals in patients with Rett syndrome by an innovative wearable technology: evidence of an overlooked chronic fatigue status
2024 S. Leoncini, L. Boasiako, S. Di Lucia, A. Beker, V. Scandurra, A. Vignoli, M.P. Canevini, G. Prato, L. Nobili, A.G. Nicotera, G. Di Rosa, M.B.T. Chiarini, R. Cutrera, S. Grosso, G. Lazzeri, E. Tongiorgi, P. Morano, M. Botteghi, A. Barducci, C. De Felice
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
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
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