1. A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome. (July 2020) Authors: Terrone, Gaetano; Marchese, Francesca; Vari, Maria Stella; Severino, Mariasavina; Madia, Francesca; Amadori, Elisabetta; Del Giudice, Ennio; Romano, Alfonso; Gennaro, Elena; Zara, Federico; Striano, Pasquale Journal: Seizure Issue: Volume 79(2020) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel c132‐134del mutation in Unverricht‐Lundborg disease and the review of literature of heterozygous compound patients. (26th November 2016) Authors: Assenza, Giovanni; Benvenga, Antonella; Gennaro, Elena; Tombini, Mario; Campana, Chiara; Assenza, Federica; Di Pino, Giovanni; Di Lazzaro, Vincenzo Journal: Epilepsia Issue: Volume 58:issue 2(2017) Page Start: e31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel mutation in KCNQ3‐related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome. Issue 1 (27th March 2019) Authors: Piro, Ettore; Nardello, Rosaria; Gennaro, Elena; Fontana, Antonina; Taglialatela, Maurizio; Mangano, Giuseppe Donato; Corsello, Giovanni; Mangano, Salvatore Journal: Epileptic disorders Issue: Volume 21:Issue 1(2019) Page Start: 87 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases. (February 2019) Authors: von Stülpnagel, Celina; Hartlieb, Till; Borggräfe, Ingo; Coppola, Antonietta; Gennaro, Elena; Eschermann, Kirsten; Kiwull, Lorenz; Kluger, Felicitas; Krois, Ilona; Møller, Rikke S.; Rössler, Franziska; Santulli, Lia; Schwermer, Constanze; Wallacher-Scholz, Barbara; Zara, Federico; Wolf, Peter; Kl... Journal: Seizure Issue: Volume 65(2019) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022) Authors: Balagura, Ganna; Xian, Julie; Riva, Antonella; Marchese, Francesca; Ben Zeev, Bruria; Rios, Loreto; Sirsi, Deepa; Accorsi, Patrizia; Amadori, Elisabetta; Astrea, Guja; Baldassari, Simona; Beccaria, Francesca; Boni, Antonella; Budetta, Mauro; Cantalupo, Gaetano; Capovilla, Giuseppe; Cesaroni, Elis... Journal: Neurology Issue: Volume 8:Number 3(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022) Authors: Balagura, Ganna; Xian, Julie; Riva, Antonella; Marchese, Francesca; Ben Zeev, Bruria; Rios, Loreto; Sirsi, Deepa; Accorsi, Patrizia; Amadori, Elisabetta; Astrea, Guja; Baldassari, Simona; Beccaria, Francesca; Boni, Antonella; Budetta, Mauro; Cantalupo, Gaetano; Capovilla, Giuseppe; Cesaroni, Elis... Journal: Neurology Issue: Volume 8:Number 3(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. Issue 3 (29th January 2013) Authors: Zara, Federico; Specchio, Nicola; Striano, Pasquale; Robbiano, Angela; Gennaro, Elena; Paravidino, Roberta; Vanni, Nicola; Beccaria, Francesca; Capovilla, Giuseppe; Bianchi, Amedeo; Caffi, Lorella; Cardilli, Viviana; Darra, Francesca; Bernardina, Bernardo Dalla; Fusco, Lucia; Gaggero, Roberto; Gi... Journal: Epilepsia Issue: Volume 54:Issue 3(2013:Mar.) Page Start: 425 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants. (December 2020) Authors: Malerba, Federica; Alberini, Giulio; Balagura, Ganna; Marchese, Francesca; Amadori, Elisabetta; Riva, Antonella; Vari, Maria Stella; Gennaro, Elena; Madia, Francesca; Salpietro, Vincenzo; Angriman, Marco; Giordano, Lucio; Accorsi, Patrizia; Trivisano, Marina; Specchio, Nicola; Russo, Angelo; Gobb... Journal: Neurology Issue: Volume 6:Number 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Maternal germinal mosaicism for SCN1A in sibs with a mild form of Dravet syndrome. (May 2015) Authors: Guala, Andrea; Peruzzi, Cinzia; Gennaro, Elena; Pennese, Loredana; Danesino, Cesare Journal: American journal of medical genetics Issue: Volume 167:Number 5(2015:May) Page Start: 1165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗