1. A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype. Issue 5 (25th March 2015) Authors: Romaniello, Romina; Saettini, Francesco; Panzeri, Elena; Arrigoni, Filippo; Bassi, Maria T.; Borgatti, Renato Journal: NeuroReport Issue: Volume 26:Issue 5(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non‐traumatic brain injury. (2nd December 2016) Authors: Molteni, Erika; Rocca, Maria A; Strazzer, Sandra; Pagani, Elisabetta; Colombo, Katia; Arrigoni, Filippo; Boffa, Giacomo; Copetti, Massimiliano; Pastore, Valentina; Filippi, Massimo Journal: Developmental medicine & child neurology Issue: Volume 59:Number 2(2017) Page Start: 199 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. A robust deconvolution method to disentangle multiple water pools in diffusion MRI. (27th July 2018) Authors: De Luca, Alberto; Leemans, Alexander; Bertoldo, Alessandra; Arrigoni, Filippo; Froeling, Martijn Journal: NMR in biomedicine Issue: Volume 31:Number 11(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome. (2nd March 2021) Authors: Masnada, Silvia; Pichiecchio, Anna; Formica, Manuela; Arrigoni, Filippo; Borrelli, Paola; Accorsi, Patrizia; Bonanni, Paolo; Borgatti, Renato; Bernardina, Bernardo Dalla; Danieli, Alberto; Darra, Francesca; Deconinck, Nicolas; De Giorgis, Valentina; Dulac, Olivier; Gataullina, Svetlana; Giordano,... Journal: Neurology Issue: Volume 96:Number 9(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Biallelic loss of EMC10 leads to mild to severe intellectual disability. Issue 7 (9th June 2022) Authors: Kaiyrzhanov, Rauan; Rocca, Clarissa; Suri, Mohnish; Gulieva, Sughra; Zaki, Maha S.; Henig, Noa Z.; Siquier, Karine; Guliyeva, Ulviyya; Mounir, Samir M.; Marom, Daphna; Allahverdiyeva, Aynur; Megahed, Hisham; van Bokhoven, Hans; Cantagrel, Vincent; Rad, Aboulfazl; Pourkeramti, Alemeh; Dehghani, Bo... Journal: Annals of clinical and translational neurology Issue: Volume 9:Issue 7(2022) Page Start: 1080 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Brain malformations and mutations in α‐ and β‐tubulin genes: a review of the literature and description of two new cases. (7th January 2014) Authors: Romaniello, Romina; Arrigoni, Filippo; Cavallini, Anna; Tenderini, Erika; Baschirotto, Cinzia; Triulzi, Fabio; Bassi, Maria‐Teresa; Borgatti, Renato Journal: Developmental medicine & child neurology Issue: Volume 56:Number 4(2014:Apr.) Page Start: 354 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Brain Structure and Degeneration Staging in Friedreich Ataxia: Magnetic Resonance Imaging Volumetrics from the ENIGMA‐Ataxia Working Group. Issue 4 (17th September 2021) Authors: Harding, Ian H.; Chopra, Sidhant; Arrigoni, Filippo; Boesch, Sylvia; Brunetti, Arturo; Cocozza, Sirio; Corben, Louise A.; Deistung, Andreas; Delatycki, Martin; Diciotti, Stefano; Dogan, Imis; Evangelisti, Stefania; França, Marcondes C.; Göricke, Sophia L.; Georgiou‐Karistianis, Nellie; Gramegna, ... Journal: Annals of neurology Issue: Volume 90:Issue 4(2021) Page Start: 570 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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) ↗
10. Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). Issue 4 (29th January 2018) Authors: Kurtas, Nehir; Arrigoni, Filippo; Errichiello, Edoardo; Zucca, Claudio; Maghini, Cristina; D'Angelo, Maria Grazia; Beri, Silvana; Giorda, Roberto; Bertuzzo, Sara; Delledonne, Massimo; Xumerle, Luciano; Rossato, Marzia; Zuffardi, Orsetta; Bonaglia, Maria Clara Journal: Journal of medical genetics Issue: Volume 55:Issue 4(2018) Page Start: 269 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗