1. ''Eye of tiger sign" mimic in patients with spastic paraplegia gene 7 (SPG7) mutations. (December 2020) Authors: Rizzo, Giovanni; Tonon, Caterina; Gramegna, Laura Ludovica; Bassi, Maria Teresa; Lodi, Raffaele; Liguori, Rocco Journal: Parkinsonism & related disorders Issue: Volume 81(2020) Page Start: 158 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. (January 2014) Authors: Costa, Cinzia; Prontera, Paolo; Sarchielli, Paola; Tonelli, Alessandra; Bassi, Maria Teresa; Cupini, Letizia Maria; Caproni, Stefano; Siliquini, Sabrina; Donti, Emilio; Calabresi, Paolo Journal: Cephalalgia Issue: Volume 34:Number 1(2014) Page Start: 68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel KCNQ3 gene mutation in a child with infantile convulsions and partial epilepsy with centrotemporal spikes. (January 2015) Authors: Fusco, Carlo; Frattini, Daniele; Bassi, Maria Teresa Journal: European journal of paediatric neurology Issue: Volume 19:Number 1(2015:Jan.) Page Start: 102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern. (February 2014) Authors: Romaniello, Romina; Zucca, Claudio; Tenderini, Erika; Arrigoni, Filippo; Ragona, Francesca; Zorzi, Giovanna; Bassi, Maria Teresa; Borgatti, Renato Journal: Journal of child neurology Issue: Volume 29:Number 2(2014:Feb.) Page Start: 249 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism. Issue 1 (2nd January 2019) Authors: Zecchini, Silvia; Giovarelli, Matteo; Perrotta, Cristiana; Morisi, Federica; Touvier, Thierry; Di Renzo, Ilaria; Moscheni, Claudia; Bassi, Maria Teresa; Cervia, Davide; Sandri, Marco; Clementi, Emilio; De Palma, Clara Journal: Autophagy Issue: Volume 15:Issue 1(2019) Page Start: 58 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cerebroretinal Microangiopathy With Calcifications and Cysts Associated With CTC1 and NDP Mutations. (December 2013) Authors: Romaniello, Romina; Arrigoni, Filippo; Citterio, Andrea; Tonelli, Alessandra; Sforzini, Cinzia; Rizzari, Carmelo; Pessina, Marco; Triulzi, Fabio; Bassi, Maria Teresa; Borgatti, Renato Journal: Journal of child neurology Issue: Volume 28:Number 12(2013) Page Start: 1702 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS Registry. Issue 7 (July 2016) Authors: Bersano, Anna; Markus, Hugh Stephen; Quaglini, Silvana; Arbustini, Eloisa; Lanfranconi, Silvia; Micieli, Giuseppe; Boncoraglio, Giorgio B.; Taroni, Franco; Gellera, Cinzia; Baratta, Silvia; Penco, Silvana; Mosca, Lorena; Grasso, Maurizia; Carrera, Paola; Ferrari, Maurizio; Cereda, Cristina; Griec... Journal: Stroke Issue: Volume 47:Issue 7(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network. (30th April 2022) Authors: Rossi, Salvatore; Rubegni, Anna; Riso, Vittorio; Barghigiani, Melissa; Bassi, Maria Teresa; Battini, Roberta; Bertini, Enrico; Cereda, Cristina; Cioffi, Ettore; Criscuolo, Chiara; Dal Fabbro, Beatrice; Dato, Clemente; D'Angelo, Maria Grazia; Di Muzio, Antonio; Diamanti, Luca; Dotti, Maria Teresa;... Journal: Neurology Issue: Volume 8:Number 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Epilepsia partialis continua associated with the p.Arg403Cys variant of the DNM1L gene: an unusual clinical progression with two episodes of super‐refractory status epilepticus with a 13‐year remission interval. Issue 1 (15th February 2022) Authors: Minghetti, Sara; Giorda, Roberto; Mastrangelo, Massimo; Tassi, Laura; Zanotta, Nicoletta; Galbiati, Sara; Bassi, Maria Teresa; Zucca, Claudio Journal: Epileptic disorders Issue: Volume 24:Issue 1(2022) Page Start: 176 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Issue 1 (2nd January 2016) Authors: Klionsky, Daniel J; Abdelmohsen, Kotb; Abe, Akihisa; Abedin, Md Joynal; Abeliovich, Hagai; Acevedo Arozena, Abraham; Adachi, Hiroaki; Adams, Christopher M; Adams, Peter D; Adeli, Khosrow; Adhihetty, Peter J; Adler, Sharon G; Agam, Galila; Agarwal, Rajesh; Aghi, Manish K; Agnello, Maria; Agostinis... Journal: Autophagy Issue: Volume 12:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗