1. Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron Disorders. (2nd November 2021) Authors: Poletti, Barbara; Solca, Federica; Carelli, Laura; Diena, Alberto; Colombo, Eleonora; Torre, Silvia; Maranzano, Alessio; Greco, Lucia; Cozza, Federica; Lizio, Andrea; Ferrucci, Roberta; Girotti, Floriano; Verde, Federico; Morelli, Claudia; Lunetta, Christian; Silani, Vincenzo; Ticozzi, Nicola Journal: Neurology Issue: Volume 97:Number 18(2021) Page Start: e1835 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. F34 Anosognosia of motor deficits in Huntington's disease. (12th September 2022) Authors: Gargallo, Francesca; Paridi, Dominga; Geminiani, Giuliano; Sorbo, Francesca Del; Silani, Vincenzo; Isaias, Ioannis; Soliveri, Paola; Girotti, Floriano Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 93(2022)Supplement 1 Page Start: A48 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy. Issue 3 (1st September 2000) Authors: Soliveri, Paola; Monza, Daniela; Paridi, Dominga; Carella, Francesco; Genitrini, Silvia; Testa, Daniela; Girotti, Floriano Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 69:Issue 3(2000) Page Start: 313 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Stereotypic behaviours in frontotemporal dementia and progressive supranuclear palsy. (December 2018) Authors: Prioni, Sara; Redaelli, Veronica; Soliveri, Paola; Fetoni, Vincenza; Barocco, Federica; Caffarra, Paolo; Scaglioni, Augusto; Tramacere, Irene; Girotti, Floriano Journal: Cortex Issue: Volume 109(2018) Page Start: 272 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene. (November 2017) Authors: Ciammola, Andrea; Carrera, Paola; Di Fonzo, Alessio; Sassone, Jenny; Villa, Roberta; Poletti, Barbara; Ferrari, Maurizio; Girotti, Floriano; Monfrini, Edoardo; Buongarzone, Gabriele; Silani, Vincenzo; Cinnante, Claudia Maria; Mignogna, Maria Lidia; D'Adamo, Patrizia; Bonati, Maria Teresa Journal: Parkinsonism & related disorders Issue: Volume 44(2017) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗