1. Intrafamilial heterogeneity of clinical phenotype of PRRT2 mutations. (June 2017) Authors: Graziola, F.; Trivisano, M.; Travaglini, L.; Terracciano, A.; Bertini, E.; Specchio, N.; Curatolo, P.; Vigevano, F.; Capuano, A. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Prospective serial neuropsychological study in infants with Tuberous Sclerosis Complex (TSC): First analysis from the EPISTOP Project. (June 2017) Authors: Benvenuto, A.; Moavero, R.; Graziola, F.; Siracusano, M.; Emberti Gialloreti, L.; Aronica, E.; Jansen, A.; Jansen, F.E.; Jozwiak, S.; Kotulska-Jozwiak, K.; Kwiatkowski, D.; Lagae, L.; Curatolo, P. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Risankizumab shows faster response in bio naïve than in bio‐experienced psoriatic patients. (22nd June 2022) Authors: Mastorino, L.; Castelli, F.; Stroppiana, E.; Verrone, A.; Ortoncelli, M.; Susca, S.; Boskovic, S.; Passerini, S.G.; Macagno, N.; Cariti, C.; Licciardello, M.; Solaroli, C.; Pertusi, G.; Aragone, M.G.; Baggini, G.; Addese, C.; Leporati, C.; Peila, R.; Giura, M.T.; Rossotto, G. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 10(2022) Page Start: e838 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗