1. A validation study of the clinical diagnosis of Dup15q syndrome: Which symptoms matter most?. (January 2020) Authors: Beghi, E.; Giussani, G.; Bianchi, E.; Randazzo, G.; Sarcona, V.; Elia, M.; Striano, P.; Verrotti, A.; Ferretti, A.; Rebessi, E.; Specchio, N.; Bonanni, P. Journal: Seizure Issue: Volume 74(2019) Page Start: 26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and genetic spectrum of SCN2A-associated episodic ataxia. (May 2019) Authors: Schwarz, N.; Bast, T.; Gaily, E.; Golla, G.; Gorman, K.M.; Griffiths, L.R.; Hahn, A.; Hukin, J.; King, M.; Korff, C.; Miranda, M.J.; Møller, R.S.; Neubauer, B.; Smith, R.A.; Smol, T.; Striano, P.; Stroud, B.; Vaccarezza, M.; Kluger, G.; Lerche, H. Journal: European journal of paediatric neurology Issue: Volume 23:Number 3(2019:May) Page Start: 438 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication. (25th October 2015) Authors: Verrotti, A.; Laino, D.; Rinaldi, V. E.; Suppiej, A.; Giordano, L.; Toldo, I.; Margari, L.; Parisi, P.; Rizzo, R.; Matricardi, S.; Cusmai, R.; Grosso, S.; Gaggero, R.; Zamponi, N.; Pavone, P.; Capovilla, G.; Rauchenzauner, M.; Cerminara, C.; Di Gennaro, G.; Esposito, M. Journal: European journal of neurology Issue: Volume 23:Number 2(2016:Feb.) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort. (December 2019) Authors: Pepi, C.; Cesaroni, E.; Striano, P.; Maiorani, D.; Pruna, D.; Cossu, S.; Di Capua, M.; Vigevano, F.; Specchio, N.; Cusmai, R. Journal: Seizure Issue: Volume 73(2019) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Early‐onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. Issue 5 (30th September 2012) Authors: Agostinelli, S.; Traverso, M.; Accorsi, P.; Beccaria, F.; Belcastro, V.; Capovilla, G.; Cappanera, S.; Coppola, A.; Dalla Bernardina, B.; Darra, F.; Ferretti, M.; Elia, M.; Galeone, D.; Giordano, L.; Gobbi, G.; Nicita, F.; Parisi, P.; Pezzella, M.; Spalice, A.; Striano, S. Journal: European journal of neurology Issue: Volume 20:Issue 5(2013:May) Page Start: 856 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Electroclinical findings and long‐term outcomes in epileptic patients with inv dup (15). (23rd January 2018) Authors: Matricardi, S.; Darra, F.; Spalice, A.; Basti, C.; Fontana, E.; Dalla Bernardina, B.; Elia, M.; Giordano, L.; Accorsi, P.; Cusmai, R.; De Liso, P.; Romeo, A.; Ragona, F.; Granata, T.; Concolino, D.; Carotenuto, M.; Pavone, P.; Pruna, D.; Striano, P.; Savasta, S. Journal: Acta neurologica Scandinavica Issue: Volume 137:Number 6(2018) Page Start: 575 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7. (July 2018) Authors: Orsini, A.; Bonuccelli, A.; Striano, P.; Azzara, A.; Costagliola, G.; Consolini, R.; Peroni, D.G.; Valetto, A.; Bertini, V. Journal: Seizure Issue: Volume 59(2018) Page Start: 38 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Interictal and periictal headache in patients with epilepsy: migraine‐triggered seizures or epilepsy‐triggered headache?. Issue 10 (24th December 2012) Authors: Belcastro, V.; Striano, P.; Parisi, P. Journal: European journal of neurology Issue: Volume 20:Issue 10(2013:Oct.) Page Start: 1333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Pediatric moyamoya disease and syndrome in Italy: Data from the Italian Society of Pediatric Neurology multicentric retrospective study. (June 2017) Authors: Sartori, S.; Po', C.; Carai, A.; Rosati, A.; Accorsi, P.; Iodice, A.; Savasta, S.; D'Avella, D.; Greco, F.; Raviglione, F.; Ragazzi, P.; Agostini, M.; Cesaroni, E.; Di Rosa, G.; Striano, P.; Nicita, F.; Cordelli, D.; Suppiej, A.; Nosadini, M.; Marras, C.E. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e151 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features. Issue 3 (11th May 2018) Authors: Ricotti, R.; Nardo, T.; Striano, P.; Stefanini, M.; Orioli, D.; Botta, E. Journal: Clinical genetics Issue: Volume 94:Issue 3/4(2018) Page Start: 386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗