Biella Fabio

Soft cerebellar signs unveil RARS2‐related epilepsy / V. Yahya, R. Dilena, R. DEL BO, M. Magni, F. Biella, S. Salani, F. Fortunato, E. Scola, A. Di Fonzo, E. Monfrini. - In: EPILEPTIC DISORDERS. - ISSN 1294-9361. - 26:4(2024 Aug), pp. 540-543. [10.1002/epd2.20237]

Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis / S.K. Aburahma, L.A. Rousan, M. Shboul, F. Biella, S. Lucchiari, G.P. Comi, G. Meola, S. Pagliarani. - In: FRONTIERS IN NEUROLOGY. - ISSN 1664-2295. - 15:(2024), pp. 1359479.1-1359479.8. [10.3389/fneur.2024.1359479]

Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency / E. Monfrini, A. Pesini, F. Biella, C.F.R. Sobreira, V. Emmanuele, G. Brescia, L.C. Lopez, S. Tadesse, M. Hirano, G.P. Comi, C.M. Quinzii, A. Di Fonzo. - In: NEUROLOGY. GENETICS. - ISSN 2376-7839. - 9:2(2023 Apr), pp. e200058.1-e200058.7. [10.1212/NXG.0000000000200058]

Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes / M. Rizzuti, V. Melzi, D. Gagliardi, D. Resnati, M. Meneri, L. Dioni, P. Masrori, N. Hersmus, K. Poesen, M. Locatelli, F. Biella, R. Silipigni, V. Bollati, N. Bresolin, G.P. Comi, P. Van Damme, M. Nizzardo, S. Corti. - In: CELLULAR AND MOLECULAR LIFE SCIENCES. - ISSN 1420-682X. - 79:3(2022 Mar 14), pp. 189.1-189.16. [10.1007/s00018-022-04217-1]

Morpholino oligomers ameliorates pathological hallmarks in C9orf72 cellular lines and mice / M. Bersani, D. Gagliardi, M. Taiana, F. Biella, M. Nizzardo, S. Corti. ((Intervento presentato al convegno Virtual ENCALS Meeting : European Network to Cure ALS tenutosi a online nel 2021.