1. A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. (April 2019) Authors: Graziola, Federica; Stregapede, Fabrizia; Travaglini, Lorena; Garone, Giacomo; Verardo, Margherita; Bosco, Luca; Pro, Stefano; Bertini, Enrico; Curatolo, Paolo; Vigevano, Federico; Capuano, Alessandro Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acute ataxia in paediatric emergency departments: a multicentre Italian study. Issue 8 (4th April 2019) Authors: Garone, Giacomo; Reale, Antonino; Vanacore, Nicola; Parisi, Pasquale; Bondone, Claudia; Suppiej, Agnese; Brisca, Giacomo; Calistri, Lucia; Cordelli, Duccio Maria; Savasta, Salvatore; Grosso, Salvatore; Midulla, Fabio; Falsaperla, Raffaele; Verrotti, Alberto; Bozzola, Elena; Vassia, Cristina; Da D... Journal: Archives of disease in childhood Issue: Volume 104:Issue 8(2019) Page Start: 768 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Acute ataxia in paediatric emergency departments: a multicentre Italian study. Issue 8 (4th August 2019) Authors: Garone, Giacomo; Reale, Antonino; Vanacore, Nicola; Parisi, Pasquale; Bondone, Claudia; Suppiej, Agnese; Brisca, Giacomo; Calistri, Lucia; Cordelli, Duccio Maria; Savasta, Salvatore; Grosso, Salvatore; Midulla, Fabio; Falsaperla, Raffaele; Verrotti, Alberto; Bozzola, Elena; Vassia, Cristina; Da D... Journal: Archives of disease in childhood Issue: Volume 104:Issue 8(2019) Page Start: 768 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Acute hyperkinetic movement disorders in Italian paediatric emergency departments. Issue 8 (8th March 2018) Authors: Raucci, Umberto; Parisi, Pasquale; Vanacore, Nicola; Garone, Giacomo; Bondone, Claudia; Palmieri, Antonella; Calistri, Lucia; Suppiej, Agnese; Falsaperla, Raffaele; Capuano, Alessandro; Ferro, Valentina; Urbino, Antonio Francesco; Tallone, Ramona; Montemaggi, Alessandra; Sartori, Stefano; Pavone,... Journal: Archives of disease in childhood Issue: Volume 103:Issue 8(2018) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Acute strabismus in neurological emergencies of childhood: A retrospective, single-centre study. (May 2021) Authors: Garone, Giacomo; Ferro, Valentina; Barbato, Marta; Vanacore, Nicola; Papini, Laura; Pro, Stefano; Boni, Alessandra; Scialanga, Barbara; Nacca, Raffaella; Evangelisti, Melania; Di Nardo, Giovanni; Parisi, Pasquale; Raucci, Umberto Journal: European journal of paediatric neurology Issue: Volume 32(2021) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Early Myoclonic Encephalopathy in 9q33‐q34 Deletion Encompassing STXBP1 and SPTAN1. (16th March 2015) Authors: Nicita, Francesco; Ulgiati, Fiorenza; Bernardini, Laura; Garone, Giacomo; Papetti, Laura; Novelli, Antonio; Spalice, Alberto Journal: Annals of human genetics Issue: Volume 79:Number 3(2015:May) Page Start: 209 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Epilepsy is a possible feature in Williams‐Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region. Issue 1 (5th October 2015) Authors: Nicita, Francesco; Garone, Giacomo; Spalice, Alberto; Savasta, Salvatore; Striano, Pasquale; Pantaleoni, Chiara; Spartà, Maria Valentina; Kluger, Gerhard; Capovilla, Giuseppe; Pruna, Dario; Freri, Elena; D'Arrigo, Stefano; Verrotti, Alberto Journal: American journal of medical genetics Issue: Volume 170:Issue 1(2016) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Highlighting the Dystonic Phenotype Related to GNAO1. Issue 7 (20th June 2022) Authors: Wirth, Thomas; Garone, Giacomo; Kurian, Manju A.; Piton, Amélie; Millan, Francisca; Telegrafi, Aida; Drouot, Nathalie; Rudolf, Gabrielle; Chelly, Jamel; Marks, Warren; Burglen, Lydie; Demailly, Diane; Coubes, Phillipe; Castro‐Jimenez, Mayte; Joriot, Sylvie; Ghoumid, Jamal; Belin, Jérémie; Faucheu... Journal: Movement disorders Issue: Volume 37:Issue 7(2022) Page Start: 1547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Impact of Italian lockdown on Tourette's syndrome patients at the time of the COVID‐19 pandemic. Issue 11 (2nd September 2020) Authors: Graziola, Federica; Garone, Giacomo; Di Criscio, Lorena; Grasso, Melissa; Curatolo, Paolo; Vigevano, Federico; Capuano, Alessandro Journal: Psychiatry and clinical neurosciences Issue: Volume 74:Issue 11(2020) Page Start: 610 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review. (April 2019) Authors: Schirinzi, Tommaso; Garone, Giacomo; Travaglini, Lorena; Vasco, Gessica; Galosi, Serena; Rios, Loreto; Castiglioni, Claudia; Barassi, Claudia; Battaglia, Domenica; Gambardella, Maria Luigia; Cantonetti, Laura; Graziola, Federica; Marras, Carlo Efisio; Castelli, Enrico; Bertini, Enrico; Capuano, A... Journal: Parkinsonism & related disorders Issue: Volume 61(2019) Page Start: 19 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗