1. A novel Xp22.13 microdeletion in Nance‐Horan syndrome. Issue 11 (2nd May 2017) Authors: Accogli, Andrea; Traverso, Monica; Madia, Francesca; Bellini, Tommaso; Vari, Maria Stella; Pinto, Francesca; Capra, Valeria Journal: Birth defects research Issue: Volume 109:Issue 11(2017) Page Start: 866 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia. Issue 1 (8th November 2021) Authors: Gemelli, Chiara; Traverso, Monica; Trevisan, Lucia; Fabbri, Sabrina; Scarsi, Elena; Carlini, Barbara; Prada, Valeria; Mongini, Tiziana; Ruggiero, Lucia; Patrone, Serena; Gallone, Salvatore; Iodice, Rosa; Pisciotta, Livia; Zara, Federico; Origone, Paola; Rota, Eugenia; Minetti, Carlo; Bruno, Claud... Journal: Muscle & nerve Issue: Volume 65:Issue 1(2022) Page Start: 96 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical dissection of early onset absence epilepsy in children and prognostic implications. Issue 10 (27th August 2013) Authors: Agostinelli, Sergio; Accorsi, Patrizia; Beccaria, Francesca; Belcastro, Vincenzo; Canevini, Maria Paola; Capovilla, Giuseppe; Cappanera, Silvia; Bernardina, Bernardo Dalla; Darra, Francesca; Gaudio, Luigi Del; Elia, Maurizio; Falsaperla, Raffaele; Giordano, Lucio; Gobbi, Giuseppe; Minetti, Carlo;... Journal: Epilepsia Issue: Volume 54:Issue 10(2013:Oct.) Page Start: 1761 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy. (April 2018) Authors: Stella Vari, Maria; Traverso, Monica; Bellini, Tommaso; Madia, Francesca; Pinto, Francesca; Striano, Pasquale; Minetti, Carlo; Zara, Federico Journal: Seizure Issue: Volume 57(2018) Page Start: 63 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy. (August 2017) Authors: Vari, Maria Stella; Traverso, Monica; Bellini, Tommaso; Madia, Francesca; Pinto, Francesca; Minetti, Carlo; Striano, Pasquale; Zara, Federico Journal: Seizure Issue: Volume 50(2017) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion. Issue 5 (28th February 2013) Authors: Coppola, Antonietta; Bagnasco, Irene; Traverso, Monica; Brusco, Alfredo; Di Gregorio, Eleonora; Del Gaudio, Luigi; Santulli, Lia; Caccavale, Carmela; Vigliano, Piernanda; Minetti, Carlo; Striano, Salvatore; Zara, Federico; Striano, Pasquale Journal: Epilepsia Issue: Volume 54:Issue 5(2013:May) Page Start: e69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Erratum to "De novo 12q22.q23.3 duplication associated with temporal lobe epilepsy" [Seizure 57 (2018) 63–65]. (April 2018) Authors: Vari, Maria Stella; Traverso, Monica; Bellini, Tommaso; Madia, Francesca; Pinto, Francesca; Striano, Pasquale; Minetti, Carlo; Zara, Federico Journal: Seizure Issue: Volume 57(2018) Page Start: R1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy. Issue 2 (20th May 2014) Authors: Vanni, Nicola; Fruscione, Floriana; Ferlazzo, Edoardo; Striano, Pasquale; Robbiano, Angela; Traverso, Monica; Sander, Thomas; Falace, Antonio; Gazzerro, Elisabetta; Bramanti, Placido; Bielawski, Jacek; Fassio, Anna; Minetti, Carlo; Genton, Pierre; Zara, Federico Journal: Annals of neurology Issue: Volume 76:Issue 2(2014:Aug.) Page Start: 206 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy. (8th March 2016) Authors: Stamberger, Hannah; Nikanorova, Marina; Willemsen, Marjolein H.; Accorsi, Patrizia; Angriman, Marco; Baier, Hartmut; Benkel-Herrenbrueck, Ira; Benoit, Valérie; Budetta, Mauro; Caliebe, Almuth; Cantalupo, Gaetano; Capovilla, Giuseppe; Casara, Gianluca; Courage, Carolina; Deprez, Marie; Destrée, An... Journal: Neurology Issue: Volume 86:Number 10(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment. (10th August 2022) Authors: Fiorillo, Chiara; Capodivento, Giovanna; Geroldi, Alessandro; Tozza, Stefano; Moroni, Isabella; Mohassel, Payam; Cataldi, Matteo; Campana, Chiara; Morando, Simone; Panicucci, Chiara; Pedemonte, Marina; Brolatti, Noemi; Siliquini, Sabrina; Traverso, Monica; Baratto, Serena; Debellis, Doriana; Magr... Journal: Neuropathology & applied neurobiology Issue: Volume 48:Number 7(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗