1. An Italian consensus on the management of Lennox-Gastaut syndrome. (October 2022) Authors: Riva, Antonella; Coppola, Antonietta; Bonaventura, Carlo Di; Elia, Maurizio; Ferlazzo, Edoardo; Gobbi, Giuseppe; Marini, Carla; Meletti, Stefano; Romeo, Antonino; Santoro, Katia; Verrotti, Alberto; Capovilla, Giuseppe; Striano, Pasquale; Aguglia, Umberto; Bagnasco, Irene; Bartolini, Emanuele; Bat... Journal: Seizure Issue: Volume 101(2022) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation. (October 2017) Authors: Bernardo, Pia; Galletta, Diana; Iasevoli, Felice; D'Ambrosio, Luigi; Troisi, Serena; Gennaro, Elena; Zara, Federico; Striano, Salvatore; de Bartolomeis, Andrea; Coppola, Antonietta Journal: Seizure Issue: Volume 51(2017) Page Start: 186 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical evolution and epilepsy outcome in three patients with CDKL5‐related developmental encephalopathy. Issue 3 (17th July 2019) Authors: Bernardo, Pia; Ferretti, Alessandro; Terrone, Gaetano; Santoro, Claudia; Bravaccio, Carmela; Striano, Salvatore; Coppola, Antonietta; Striano, Pasquale Journal: Epileptic disorders Issue: Volume 21:Issue 3(2019) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. High-functioning autism spectrum disorder with fluent speech and late-onset epilepsy: an unusual presentation of Inv-Dup (15) syndrome. Issue 1 (4th March 2019) Authors: Bernardo, Pia; Del Gaudio, Luigi; Madia, Francesca; Riccio, Maria Pia; Marino, Maria; Santoro, Claudia; Caccavale, Carmela; Striano, Salvatore; Bravaccio, Carmela; Coppola, Antonietta Journal: Neurocase Issue: Volume 25:Issue 1/2(2019) Page Start: 62 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy. (September 2020) Authors: Terrone, Gaetano; Pinelli, Michele; Bernardo, Pia; Parrini, Elena; Imperati, Floriana; Brunetti-Pierri, Nicola; Del Giudice, Ennio Journal: European journal of paediatric neurology Issue: Volume 28(2020) Page Start: 237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Neurophysiological Signatures of Motor Impairment in Patients with Rett Syndrome. Issue 5 (17th March 2020) Authors: Bernardo, Pia; Cobb, Stuart; Coppola, Antonietta; Tomasevic, Leo; Di Lazzaro, Vincenzo; Bravaccio, Carmela; Manganelli, Fiore; Dubbioso, Raffaele Journal: Annals of neurology Issue: Volume 87:Issue 5(2020) Page Start: 763 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Pain and sleep disturbances in Rett syndrome and other neurodevelopmental disorders. (17th October 2018) Authors: Cappuccio, Gerarda; Bernardo, Pia; Raiano, Enza; Pinelli, Michele; Alagia, Marianna; Esposito, Marcello; Della Casa, Roberto; Strisciuglio, Pietro; Brunetti‐Pierri, Nicola; Bravaccio, Carmela Journal: Acta pædiatrica Issue: Volume 108:Number 1(2019) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Treatment of hypersalivation in rett syndrome with botulinum toxin: Efficacy and clinical implications. (December 2018) Authors: Esposito, Marcello; Raiano, Enza; Bernardo, Pia; Cappuccio, Gerarda; Dubbioso, Raffaele; Bravaccio, Carmela; Vergara, Emilia; Peluso, Silvio; Manganelli, Fiore Journal: Toxicon Issue: Volume 156(2018)Supplement 1 Page Start: S28 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. UBE2A deficiency in two siblings: A novel splicing variant inherited from a maternal germline mosaicism. Issue 3 (28th December 2017) Authors: Giugliano, Teresa; Santoro, Claudia; Torella, Annalaura; Del Vecchio Blanco, Francesca; Bernardo, Pia; Nigro, Vincenzo; Piluso, Giulio Journal: American journal of medical genetics Issue: Volume 176:Issue 3(2018) Page Start: 722 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Xq25 microduplication syndrome: a further contribution to its definition. A case report and review of the literature. Issue 2 (April 2020) Authors: Turchi, Giulia; Bernardo, Pia; Consales, Alessandro; Bilo, Leonilda; Coppola, Antonietta Journal: Clinical dysmorphology Issue: Volume 29:Issue 2(2020:Apr.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗