BIELLA, FABIO
BIELLA, FABIO
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis
2024 S.K. Aburahma, L.A. Rousan, M. Shboul, F. Biella, S. Lucchiari, G.P. Comi, G. Meola, S. Pagliarani
Soft cerebellar signs unveil RARS2‐related epilepsy
2024 V. Yahya, R. Dilena, R. DEL BO, M. Magni, F. Biella, S. Salani, F. Fortunato, E. Scola, A. Di Fonzo, E. Monfrini
Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency
2023 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
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes
2022 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
Morpholino oligomers ameliorates pathological hallmarks in C9orf72 cellular lines and mice
2021 M. Bersani, D. Gagliardi, M. Taiana, F. Biella, M. Nizzardo, S. Corti
INVESTIGATION OF C9ORF72 MOLECULAR HALLMARKS AND DEVELOPMENT OF THERAPEUTIC STRATEGIES
2021 F. Biella
A novel homozygous VPS11 variant may cause generalized dystonia
2021 E. Monfrini, F. Cogiamanian, S. Salani, L. Straniero, G. Fagiolari, M. Garbellini, E. Carsana, L. Borellini, F. Biella, M. Moggio, N. Bresolin, S. Corti, S. Duga, G.P. Comi, M. Aureli, A. Di Fonzo
Evaluation of Morpholino oligomers therapeutic efficacy in C9orf72 ALS iPSC-derived lines
2020 M. Bersani, M. Taiana, F. Biella, M. Nizzardo, S. Ghezzi, N. Bresolin, G.P. Comi, S. Corti
Changes in pathological phenotype of C9orf72 ALS iPSC-derived lines after treatment with Morpholino oligomers
2020 M. Bersani, M. Taiana, F. Biella, M. Nizzardo, S. Ghezzi, S. Corti
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy
2020 G. Bitetto, M.C. Malaguti, R. Ceravolo, E. Monfrini, L. Straniero, A. Morini, R. Di Giacopo, D. Frosini, G. Palermo, F. Biella, D. Ronchi, S. Duga, F. Taroni, S. Corti, G.P. Comi, N. Bresolin, B. Giometto, A. Di Fonzo
Neural stem cell transplantation for neurodegenerative diseases
2020 R. De Gioia, F. Biella, G. Citterio, F. Rizzo, E. Abati, M. Nizzardo, N. Bresolin, G.P. Comi, S. Corti
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementia
2020 D. Gagliardi, G. Costamagna, M. Taiana, L. Andreoli, F. Biella, M. Bersani, N. Bresolin, G.P. Comi, S. Corti