1. A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype. (May 2018) Authors: Iapadre, Giulia; Morana, Giovanni; Vari, Maria Stella; Pinto, Francesca; Lanteri, Paola; Tessa, Alessandra; Santorelli, Filippo Maria; Striano, Pasquale; Verrotti, Alberto Journal: European journal of paediatric neurology Issue: Volume 22:Number 3(2018:May) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An update on brivaracetam for the treatment of pediatric partial epilepsy. (24th July 2021) Authors: Tulli, Eleonora; Di Cara, Giuseppe; Iapadre, Giulia; Striano, Pasquale; Verrotti, Alberto Journal: Expert opinion on pharmacotherapy Issue: Volume 22:Number 11(2021) Page Start: 1387 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Anti-viral therapy for congenital cytomegalovirus infection: pharmacokinetics, efficacy and side effects. (18th May 2016) Authors: Mareri, Arianna; Lasorella, Stefania; Iapadre, Giulia; Maresca, Maria; Tambucci, Renato; Nigro, Giovanni Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 29:Number 10(2016) Page Start: 1657 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cessation of epilepsy therapy in children. (3rd May 2016) Authors: Stagi, Stefano; Lasorella, Stefania; Piccorossi, Alessandra; Iapadre, Giulia; Verrotti, Alberto Journal: Expert review of neurotherapeutics Issue: Volume 16:Number 5(2016) Page Start: 549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical and electroencephalographic features of epilepsy in patients with triple X syndrome: A case series. (November 2022) Authors: Dell'Isola, Giovanni Battista; Mencaroni, Elisabetta; Prontera, Paolo; Cara, Giuseppe Di; Ferraro, Luigi; Bonanni, Paolo; Carotenuto, Marco; Iapadre, Giulia; Matricardi, Sara; Operto, Francesca; Orsini, Alessandro; Parisi, Pasquale; Pavone, Piero; Salpietro, Vincenzo; Savasta, Salvatore; Striano,... Journal: Seizure Issue: Volume 102(2022) Page Start: 32 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Epilepsy, electroclinical features, and long‐term outcomes in Pitt–Hopkins syndrome due to pathogenic variants in the TCF4 gene. (7th October 2021) Authors: Matricardi, Sara; Bonanni, Paolo; Iapadre, Giulia; Elia, Maurizio; Cesaroni, Elisabetta; Danieli, Alberto; Negrin, Susanna; Zagaroli, Luca; Operto, Francesca Felicia; Carotenuto, Marco; Pisani, Francesco; Turco, Emanuela Claudia; Orsini, Alessandro; Bonuccelli, Alice; Savasta, Salvatore; Concolin... Journal: European journal of neurology Issue: Volume 29:Number 1(2022) Page Start: 19 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Intramuscular Midazolam for treatment of Status Epilepticus. (2nd January 2021) Authors: Riva, Antonella; Iapadre, Giulia; Grasso, Eleonora Agata; Balagura, Ganna; Striano, Pasquale; Verrotti, Alberto Journal: Expert opinion on pharmacotherapy Issue: Volume 22:Number 1(2021) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Ketogenic diet and childhood neurological disorders other than epilepsy: an overview. (4th May 2017) Authors: Verrotti, Alberto; Iapadre, Giulia; Pisano, Simone; Coppola, Giangennaro Journal: Expert review of neurotherapeutics Issue: Volume 17:Number 5(2017) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Moving beyond sodium valproate: choosing the right anti-epileptic drug in children. (13th August 2019) Authors: Balagura, Ganna; Iapadre, Giulia; Verrotti, Alberto; Striano, Pasquale Journal: Expert opinion on pharmacotherapy Issue: Volume 20:Number 12(2019) Page Start: 1449 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder). (September 2018) Authors: Striano, Pasquale; Iapadre, Giulia; Vari, Maria Stella; Verrotti, Alberto Journal: European journal of paediatric neurology Issue: Volume 22:Number 5(2018:Sep.) Page Start: 892 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗