1. Advances in genetic testing and optimization of clinical management in children and adults with epilepsy. (3rd March 2020) Authors: Scala, Marcello; Bianchi, Amedeo; Bisulli, Francesca; Coppola, Antonietta; Elia, Maurizio; Trivisano, Marina; Pruna, Dario; Pippucci, Tommaso; Canafoglia, Laura; Lattanzi, Simona; Franceschetti, Silvana; Nobile, Carlo; Gambardella, Antonio; Michelucci, Roberto; Zara, Federico; Striano, Pasquale Journal: Expert review of neurotherapeutics Issue: Volume 20:Number 3(2020) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation. Issue 4 (19th September 2020) Authors: Michelucci, Roberto; Dazzo, Emanuela; Volpi, Lilia; Pasini, Elena; Riguzzi, Patrizia; Minardi, Raffaella; Marliani, Anna Federica; Tappatà, Maria; Bisulli, Francesca; Tassinari, Carlo Alberto; Nobile, Carlo Journal: Epileptic disorders Issue: Volume 22:Issue 4(2020) Page Start: 443 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees. Issue 10 (19th September 2014) Authors: Fanciulli, Manuela; Pasini, Elena; Malacrida, Sandro; Striano, Pasquale; Striano, Salvatore; Michelucci, Roberto; Ottman, Ruth; Nobile, Carlo Journal: Epilepsia Issue: Volume 55:Issue 10(2014:Oct.) Page Start: 1651 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy. (27th July 2015) Authors: Striano, Pasquale; Serioli, Elena; Santulli, Lia; Manna, Ida; Labate, Angelo; Dazzo, Emanuela; Pasini, Elena; Gambardella, Antonio; Michelucci, Roberto; Striano, Salvatore; Nobile, Carlo Journal: Epilepsia Issue: Volume 56:issue 10(2015:Oct.) Page Start: e168 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epilepsy-causing Reelin mutations result in impaired secretion and intracellular degradation of mutant proteins. Issue 5 (11th September 2021) Authors: Dazzo, Emanuela; Nobile, Carlo Journal: Human molecular genetics Issue: Volume 31:Issue 5(2022) Page Start: 665 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. In response: DEPDC5 mutations in epilepsy with auditory features. (5th February 2016) Authors: Striano, Pasquale; Michelucci, Roberto; Striano, Salvatore; Nobile, Carlo Journal: Epilepsia Issue: Volume 57:issue 2(2016) Page Start: 336 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. Issue 7 (26th April 2013) Authors: Michelucci, Roberto; Pasini, Elena; Malacrida, Sandro; Striano, Pasquale; Bonaventura, Carlo Di; Pulitano, Patrizia; Bisulli, Francesca; Egeo, Gabriella; Santulli, Lia; Sofia, Vito; Gambardella, Antonio; Elia, Maurizio; de Falco, Arturo; Neve, Angela la; Banfi, Paola; Coppola, Giangennaro; Avoni,... Journal: Epilepsia Issue: Volume 54:Issue 7(2013:Jul.) Page Start: 1288 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutations in MICAL‐1cause autosomal‐dominant lateral temporal epilepsy. Issue 3 (13th March 2018) Authors: Dazzo, Emanuela; Rehberg, Kati; Michelucci, Roberto; Passarelli, Daniela; Boniver, Clementina; Vianello Dri, Valeria; Striano, Pasquale; Striano, Salvatore; Pasterkamp, R. Jeroen; Nobile, Carlo Journal: Annals of neurology Issue: Volume 83:Issue 3(2018) Page Start: 483 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The genetic basis of juvenile myoclonic epilepsy. Issue 6 (June 2018) Authors: Striano, Pasquale; Nobile, Carlo Journal: Lancet neurology Issue: Volume 17:Issue 6(2018) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Whole-exome sequencing to disentangle the complex genetics of hippocampal sclerosis–temporal lobe epilepsy. (June 2018) Authors: Striano, Pasquale; Nobile, Carlo Journal: Neurology Issue: Volume 4:Number 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗