1. Cortical network dysfunction revealed by magnetoencephalography in carriers of spinocerebellar ataxia 1 or 2 mutation. Issue 7 (July 2020) Authors: Visani, Elisa; Mariotti, Caterina; Nanetti, Lorenzo; Mongelli, Alessia; Castaldo, Anna; Panzica, Ferruccio; Rossi Sebastiano, Davide; Nigri, Anna; Grisoli, Marina; Franceschetti, Silvana; Canafoglia, Laura Journal: Clinical neurophysiology Issue: Volume 131:Issue 7(2020:Jul.) Page Start: 1548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. D14 Plasma levels of 24S-hydroxycholesterol are reduced in Huntington disease subjects: preliminary results of a 2-year longitudinal study. (12th September 2022) Authors: Fichera, Mario; Nanetti, Lorenzo; Favagrossa, Monica; Castaldo, Anna; Nigri, Anna; Mongelli, Alessia; Marchini, Gloria; Gellera, Cinzia; Grisoli, Marina; Birolini, Giulia; Valenza, Marta; Bagnati, Renzo; Passoni, Alice; Colombo, Laura; Cattaneo, Elena; Salmona, Mario; Mariotti, Caterina Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 93(2022)Supplement 1 Page Start: A25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. F6 Does premanifest HD perform worse in arithmetic? Symbol digit and calculation tests confirm early cognitive impairment in preHD and correlate with brain MRI abnormalities. (13th September 2016) Authors: Castaldo, Anna; Nanetti, Lorenzo; Bachoud-Lévi, Anne-Catherine; Giavazzi, Maria; Contarino, Valeria; Nava, Simone; Mongelli, Alessia; Gellera, Cinzia; Grisoli, Marina; Bruzzone, Maria Grazia; Bella, Daniela Di; Ciammola, Andrea; Taroni, Franco; Mariotti, Caterina Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Frataxin deficiency in Friedreich's ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival. (15th January 2020) Authors: Tiano, Francesca; Amati, Francesca; Cherubini, Fabio; Morini, Elena; Vancheri, Chiara; Maletta, Sara; Fortuni, Silvia; Serio, Dario; Quatrana, Andrea; Luffarelli, Riccardo; Benini, Monica; Alfedi, Giulia; Panarello, Luca; Rufini, Alessandra; Toschi, Nicola; Frontali, Marina; Romano, Silvia; Marco... Journal: Human molecular genetics Issue: Volume 29:Number 3(2020) Page Start: 471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. G08 An italian study to estimate the frequency of the intermediate triplet length in the huntingtin gene: 1/20 subject carries an allele with 27–35 cag. (September 2018) Authors: Nanetti, Lorenzo; Mongelli, Alessia; Castaldo, Anna; Salvatore, Elena; Rizzo, Elena; Gellera, Cinzia; Taroni, Franco; Mariotti, Caterina Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 89(2018)Supplement 1 Page Start: A68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1. Issue 12 (7th January 2022) Authors: Quatrana, Andrea; Morini, Elena; Tiano, Francesca; Vancheri, Chiara; Panarello, Luca; Romano, Silvia; Marcotulli, Christian; Casali, Carlo; Mariotti, Caterina; Mongelli, Alessia; Fichera, Mario; Rufini, Alessandra; Condò, Ivano; Novelli, Giuseppe; Testi, Roberto; Amati, Francesca; Malisan, Florence Journal: Human molecular genetics Issue: Volume 31:Issue 12(2022) Page Start: 2010 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. I16 Very slow disease progression in two hd patients carrying 40 and 45 cag repeats: a 10-year follow-up observational report. (13th September 2016) Authors: Mariotti, Caterina; Nanetti, Lorenzo; Castaldo, Anna; Mongelli, Alessia; Rizzo, Elena; Grisoli, Marina; Taroni, Franco; Gellera, Cinzia Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A64 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. JMJD3 and vascular injury: the Emperor's new clothes. Issue 14 (5th October 2018) Authors: Mongelli, Alessia; Gaetano, Carlo Journal: Cardiovascular research Issue: Volume 114:Issue 14(2018) Page Start: 1825 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout. Issue 2 (27th November 2020) Authors: Magri, Stefania; Nanetti, Lorenzo; Mongelli, Alessia; Rizzo, Elena; Taroni, Franco; Mariotti, Caterina; Gellera, Cinzia Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 397 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients. (21st June 2018) Authors: Mongelli, Alessia; Sarro, Lidia; Rizzo, Elena; Nanetti, Lorenzo; Meucci, Nicoletta; Pezzoli, Gianni; Goldwurm, Stefano; Taroni, Franco; Mariotti, Caterina; Gellera, Cinzia Journal: Neuroscience letters Issue: Volume 678(2018) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗